https://www.proteinsynthesis.org/what-is-protein-synthesis/
Protein Folding
Protein Synthesis
Definition
Protein synthesis is process in which polypeptide chains are formed from coded combinations of
single amino acids inside the cell. The synthesis of new polypeptides requires a coded sequence,
enzymes, and messenger, ribosomal, and transfer ribonucleic
acids (RNAs). Protein synthesis takes place within the nucleus
and ribosomes of a cell and is regulated by DNA and RNA.
Protein synthesis is process in which polypeptide chains are formed from coded combinations of single amino acids inside the cell. The synthesis of new polypeptides requires a coded sequence, enzymes, and messenger, ribosomal, and transfer ribonucleic acids (RNAs). Protein synthesis takes place within the nucleus and ribosomes of a cell and is regulated by DNA and RNA.
Protein Synthesis Steps
Protein synthesis steps are twofold. Firstly, the code for a
protein (a chain of amino acids in a specific order) must be
copied from the genetic information contained within a cell’s
DNA. This initial protein synthesis step is known as transcription.
Transcription produces an exact copy of a section of DNA. This
copy is known as messenger RNA (mRNA) which must then be transported outside of the cell nucleus before the next step of protein synthesis can begin.
The second protein synthesis step is translation. Translation occurs within a cell organelle called a ribosome. Messenger RNA makes its way to and connects with the ribosome
under the influence of ribosomal RNA and enzymes. Transfer RNA (tRNA) is a molecule that carries a single amino acid and a coded sequence
that acts like a key. This key fits into a specific sequence of
three codes on the mRNA, bringing the correct amino acid into
place. Each set of three mRNA nitrogenous bases is called a
codon.
Translation and transcription will be explained in much more
detail further on. In order to keep protein synthesis simple, we
first need to know the basics.
Protein synthesis steps are twofold. Firstly, the code for a protein (a chain of amino acids in a specific order) must be copied from the genetic information contained within a cell’s DNA. This initial protein synthesis step is known as transcription.
Transcription produces an exact copy of a section of DNA. This copy is known as messenger RNA (mRNA) which must then be transported outside of the cell nucleus before the next step of protein synthesis can begin.
The second protein synthesis step is translation. Translation occurs within a cell organelle called a ribosome. Messenger RNA makes its way to and connects with the ribosome under the influence of ribosomal RNA and enzymes. Transfer RNA (tRNA) is a molecule that carries a single amino acid and a coded sequence that acts like a key. This key fits into a specific sequence of three codes on the mRNA, bringing the correct amino acid into place. Each set of three mRNA nitrogenous bases is called a codon.
Translation and transcription will be explained in much more detail further on. In order to keep protein synthesis simple, we first need to know the basics.
Polypeptides and Proteins
The result of protein synthesis is a chain of amino acids that
have been attached, link by link, in a specific order. This
chain is called a polymer or polypeptide and is constructed
according to a DNA-based code. You can picture a polypeptide
chain as a string of beads, with each bead playing the part of
an amino acid. The order in which the beads are strung are
copied from instructions in our DNA.
When speaking of protein synthesis it is important to make a
distinction between polypeptide chains and proteins. All
proteins are polypeptides but not all polypeptides are proteins;
however, both proteins and polypeptides are composed of amino
acid monomers.
The difference between a protein and a polypeptide is the form.
Smaller chains of amino acids – usually less than forty – remain
as single-chain strands and are called polypeptides. Larger
chains must package themselves more tightly; they fold into
fixed structures – secondary, tertiary, and quaternary. When a
polypeptide chain folds, it is called a protein.
Polypeptide chains are formed during the translation process of
protein synthesis. These polypeptides may or may not fold into
proteins at a later stage. However, the term ‘protein synthesis’
is used even in the scientific community and is not incorrect.
Understanding protein synthesis is easy when we imagine our DNA
as a recipe book. This book lists the instructions that show a
cell how to make every tiny part of every system, organ, and tissuewithin our bodies. All of these individual parts are
polypeptides. From the keratin in your hair and fingernails to
the hormones that run through your bloodstream, polypeptides and
proteins are the foundation stones of every structure. Our DNA
does not code for lipids or carbohydrates – it only codes for
polypeptides.
The enzyme RNA polymerase opens the DNA recipe book that sits inside the cell
nucleus. It uses certain pieces of code as bookmarks to find the
right page. This recipe book is written in a foreign language –
mRNA copies what is written without understanding it. The
recipes are translated into a language that other molecules can
decipher at a later stage. The translators are ribosomes and
tRNA. They read the recipe and can collect the right ingredients
and, in the correct order, make the finished polypeptide
product.
The result of protein synthesis is a chain of amino acids that have been attached, link by link, in a specific order. This chain is called a polymer or polypeptide and is constructed according to a DNA-based code. You can picture a polypeptide chain as a string of beads, with each bead playing the part of an amino acid. The order in which the beads are strung are copied from instructions in our DNA.
When speaking of protein synthesis it is important to make a distinction between polypeptide chains and proteins. All proteins are polypeptides but not all polypeptides are proteins; however, both proteins and polypeptides are composed of amino acid monomers.
The difference between a protein and a polypeptide is the form. Smaller chains of amino acids – usually less than forty – remain as single-chain strands and are called polypeptides. Larger chains must package themselves more tightly; they fold into fixed structures – secondary, tertiary, and quaternary. When a polypeptide chain folds, it is called a protein.
Polypeptide chains are formed during the translation process of protein synthesis. These polypeptides may or may not fold into proteins at a later stage. However, the term ‘protein synthesis’ is used even in the scientific community and is not incorrect.
Understanding protein synthesis is easy when we imagine our DNA as a recipe book. This book lists the instructions that show a cell how to make every tiny part of every system, organ, and tissuewithin our bodies. All of these individual parts are polypeptides. From the keratin in your hair and fingernails to the hormones that run through your bloodstream, polypeptides and proteins are the foundation stones of every structure. Our DNA does not code for lipids or carbohydrates – it only codes for polypeptides.
The enzyme RNA polymerase opens the DNA recipe book that sits inside the cell nucleus. It uses certain pieces of code as bookmarks to find the right page. This recipe book is written in a foreign language – mRNA copies what is written without understanding it. The recipes are translated into a language that other molecules can decipher at a later stage. The translators are ribosomes and tRNA. They read the recipe and can collect the right ingredients and, in the correct order, make the finished polypeptide product.
DNA Sequences
In the nucleus, two strands of DNA are held together by
nitrogenous bases (also called nucleobases or bases). Four bases
– cytosine, guanine, adenine, and thymine – form the letters of the words in the DNA recipe book.
One strand of DNA holds the original code. If the instructions
of this code are carefully followed, a specific correct
polypeptide can be assembled outside the nucleus. The second DNA
strand – the template strand – is a mirror image of the original
strand. It must be a mirror image as nucleobases can only attach
to complementary partners. For example, cytosine only ever pairs
with guanine and thymine only pairs with adenine.
You will probably have seen codes such as CTA, ATA, TAA, and CCC
in various biology textbooks. If these are the codons (sets of
three bases) of the original strand of DNA, the template strand
will attach to these using their partners. So using the given
examples, template DNA will attach to the original DNA strand
using GAT, TAT, ATT, and GGG.
Messenger RNA then copies the template strand. This means it
ends up creating an exact copy of the original strand. The only
difference is that mRNA replaces thymine with a base called
uracil. The mRNA copy of the template strand using the given
examples would read CUA, AUA, UAA, and CCC.
These codes can be read by transfer RNA outside the nucleus; the
recipe can be understood by a molecule that does not fully
understand the language used in the original (it does not
understand thymine, only uracil). Transfer RNA helps to bring
the right parts to the assembly line of the ribosome. There, a
protein chain is constructed that matches the instructions in
the original DNA strand.
In the nucleus, two strands of DNA are held together by nitrogenous bases (also called nucleobases or bases). Four bases – cytosine, guanine, adenine, and thymine – form the letters of the words in the DNA recipe book.
One strand of DNA holds the original code. If the instructions of this code are carefully followed, a specific correct polypeptide can be assembled outside the nucleus. The second DNA strand – the template strand – is a mirror image of the original strand. It must be a mirror image as nucleobases can only attach to complementary partners. For example, cytosine only ever pairs with guanine and thymine only pairs with adenine.
You will probably have seen codes such as CTA, ATA, TAA, and CCC in various biology textbooks. If these are the codons (sets of three bases) of the original strand of DNA, the template strand will attach to these using their partners. So using the given examples, template DNA will attach to the original DNA strand using GAT, TAT, ATT, and GGG.
Messenger RNA then copies the template strand. This means it ends up creating an exact copy of the original strand. The only difference is that mRNA replaces thymine with a base called uracil. The mRNA copy of the template strand using the given examples would read CUA, AUA, UAA, and CCC.
These codes can be read by transfer RNA outside the nucleus; the recipe can be understood by a molecule that does not fully understand the language used in the original (it does not understand thymine, only uracil). Transfer RNA helps to bring the right parts to the assembly line of the ribosome. There, a protein chain is constructed that matches the instructions in the original DNA strand.
Protein Synthesis Contributors
To make the copied stretch of code (transcription) we need
enzymes called RNA polymerases. These enzymes gather
free-floating messenger RNA (mRNA) molecules inside the nucleus
and assemble them to form the letters of the code. Each letter
of DNA code has its own key and each new letter formed by mRNA
carries a lock that suits this key, a little like tRNA.
Notice that we are talking about letters. This is important.
Inside the nucleus, the DNA code is not understood, simply
copied down – transcribed. Understanding the code by spelling
out the words formed by these letters – translating –
happens at a later stage.
RNA polymerase must find and bring over the appropriate mRNA
molecule for each nitrogenous base on the template strand. Selected mRNA molecules link
together to form a chain of letters. Eventually, these letters
will spell out the equivalent of a phrase. Each phrase
represents a specific (polypeptide) product. If the recipe is
not exactly followed, the final product might be completely
different or not work as well as it should.
Messenger RNA has now become the code. It travels to the next
group of important contributors that work as manufacturing
plants. Ribosomes are found outside the cell nucleus, either in
the cell cytoplasm or attached to the rough endoplasmic reticulum; it is ribosomes that make the endoplasmic reticulum ‘rough’.
A ribosome is split into two parts and the strand of mRNA runs
through it like ribbon through an old-fashioned typewriter. The
ribosome recognizes and connects to a special code at the start
of the translated phrase – the start codon. Transfer RNA molecules enter the ribosome, bringing with them
individual ingredients. As with all of these processes, enzymes
are required to make the connections.
If each mRNA codon has a lock, tRNA possesses the keys. The tRNA
key for an mRNA codon is called an anticodon. When a tRNA molecule holds the key that matches a
three-nucleobase code it can open the door, drop off its load
(an amino acid), and leave the ribosome factory to collect
another amino acid load. This will always be the same type of
amino acid as the anticodon.
Messenger RNA shifts along the ribosome as if on a conveyor
belt. At the next codon another tRNA molecule (with the right
key) brings the next amino acid. This amino acid bonds to the
previous one. A chain of bonded amino acids begins to form– a
polypeptide chain. When completed, this polypeptide chain is an
accurate final product manufactured according to the
instructions in the DNA recipe book. Not a pie or a cake but a
polypeptide chain.
The end of the mRNA code translation process is signaled by
a stop codon. Start and stop codons do not code for amino acids but tell
the tRNA and ribosome where a polypeptide chain should begin and
end.
The finished product – the newly synthesized polypeptide – is
released into the cytoplasm. From there it can travel to
wherever it is needed.
To make the copied stretch of code (transcription) we need enzymes called RNA polymerases. These enzymes gather free-floating messenger RNA (mRNA) molecules inside the nucleus and assemble them to form the letters of the code. Each letter of DNA code has its own key and each new letter formed by mRNA carries a lock that suits this key, a little like tRNA.
Notice that we are talking about letters. This is important. Inside the nucleus, the DNA code is not understood, simply copied down – transcribed. Understanding the code by spelling out the words formed by these letters – translating – happens at a later stage.
RNA polymerase must find and bring over the appropriate mRNA molecule for each nitrogenous base on the template strand. Selected mRNA molecules link together to form a chain of letters. Eventually, these letters will spell out the equivalent of a phrase. Each phrase represents a specific (polypeptide) product. If the recipe is not exactly followed, the final product might be completely different or not work as well as it should.
Messenger RNA has now become the code. It travels to the next group of important contributors that work as manufacturing plants. Ribosomes are found outside the cell nucleus, either in the cell cytoplasm or attached to the rough endoplasmic reticulum; it is ribosomes that make the endoplasmic reticulum ‘rough’.
A ribosome is split into two parts and the strand of mRNA runs through it like ribbon through an old-fashioned typewriter. The ribosome recognizes and connects to a special code at the start of the translated phrase – the start codon. Transfer RNA molecules enter the ribosome, bringing with them individual ingredients. As with all of these processes, enzymes are required to make the connections.
If each mRNA codon has a lock, tRNA possesses the keys. The tRNA key for an mRNA codon is called an anticodon. When a tRNA molecule holds the key that matches a three-nucleobase code it can open the door, drop off its load (an amino acid), and leave the ribosome factory to collect another amino acid load. This will always be the same type of amino acid as the anticodon.
Messenger RNA shifts along the ribosome as if on a conveyor belt. At the next codon another tRNA molecule (with the right key) brings the next amino acid. This amino acid bonds to the previous one. A chain of bonded amino acids begins to form– a polypeptide chain. When completed, this polypeptide chain is an accurate final product manufactured according to the instructions in the DNA recipe book. Not a pie or a cake but a polypeptide chain.
The end of the mRNA code translation process is signaled by a stop codon. Start and stop codons do not code for amino acids but tell the tRNA and ribosome where a polypeptide chain should begin and end.
The finished product – the newly synthesized polypeptide – is released into the cytoplasm. From there it can travel to wherever it is needed.
Site of Protein Synthesis
The site of protein synthesis is twofold. Transcription (copying
the code) occurs within the cell nucleus where DNA is located.
Once the mRNA copy of a small section of DNA has been made it
travels through the nuclear pores and into the cell cytoplasm.
In the cytoplasm, the strand of mRNA will move towards a free
ribosome or one attached to the rough endoplasmic reticulum.
Then the next step of protein synthesis – translation – can
begin.
The site of protein synthesis is twofold. Transcription (copying the code) occurs within the cell nucleus where DNA is located. Once the mRNA copy of a small section of DNA has been made it travels through the nuclear pores and into the cell cytoplasm. In the cytoplasm, the strand of mRNA will move towards a free ribosome or one attached to the rough endoplasmic reticulum. Then the next step of protein synthesis – translation – can begin.
New Roles for Ribosomes
The average mammalian cell contains more than ten million
ribosomes. Cancer cells can produce up to 7,500 ribosomal
subunits (small and large) every minute. As a
polypeptide-producing factory, the existence, development, and
function of every living organismdepends on the ribosome.
It was previously thought that eukaryotic ribosomes only played
effector roles in protein synthesis (caused an effect – a new
protein). However, recent research now shows that ribosomes also
regulate the translation process. They play a part in deciding
which proteins are manufactured and in what quantities. The
success and results of translation depend on more than the
availability of free amino acids and enzymes – they also
depend on the quality of the ribosomes.
The average mammalian cell contains more than ten million ribosomes. Cancer cells can produce up to 7,500 ribosomal subunits (small and large) every minute. As a polypeptide-producing factory, the existence, development, and function of every living organismdepends on the ribosome.
It was previously thought that eukaryotic ribosomes only played effector roles in protein synthesis (caused an effect – a new protein). However, recent research now shows that ribosomes also regulate the translation process. They play a part in deciding which proteins are manufactured and in what quantities. The success and results of translation depend on more than the availability of free amino acids and enzymes – they also depend on the quality of the ribosomes.
Transcription in Protein Synthesis
The transcription process is the first step of protein
synthesis. This step transfers genetic information from DNA to
the ribosomes of the cytoplasm or rough endoplasmic reticulum.
Transcription is divided into three phases: initiation,
elongation and termination.
The transcription process is the first step of protein synthesis. This step transfers genetic information from DNA to the ribosomes of the cytoplasm or rough endoplasmic reticulum. Transcription is divided into three phases: initiation, elongation and termination.
Initiation
Initiation requires two special protein groups. The first group
is transcription factors – these recognize promoter sequences in
the DNA. A promoter sequence is a section of code found at the
start of a single gene that shows where the copying process should begin and in
which direction this code should be read. A promoter works a
little like the start codon on mRNA.
The second protein group necessary for transcription initiation
consists of DNA-dependent RNA polymerases (RNAPs). An RNA
polymerase molecule binds to the promoter. Once this connection
has been made, the double-stranded DNA unwinds and opens
(unzips).
Connected bases keep the two strands of DNA in a double-helix
form. When the two strands unzip, the individual and now
unpartnered bases are left exposed. The unzipping process is
repeated along the stretch of DNA by RNAPs until the
transcription stop point or terminator is reached. Intitiation,
therefore, involves the recognition of a promotor sequence and
the unzipping of a section of DNA under the influence of
transcription factors and RNA polymerases.
Initiation requires two special protein groups. The first group is transcription factors – these recognize promoter sequences in the DNA. A promoter sequence is a section of code found at the start of a single gene that shows where the copying process should begin and in which direction this code should be read. A promoter works a little like the start codon on mRNA.
The second protein group necessary for transcription initiation consists of DNA-dependent RNA polymerases (RNAPs). An RNA polymerase molecule binds to the promoter. Once this connection has been made, the double-stranded DNA unwinds and opens (unzips).
Connected bases keep the two strands of DNA in a double-helix form. When the two strands unzip, the individual and now unpartnered bases are left exposed. The unzipping process is repeated along the stretch of DNA by RNAPs until the transcription stop point or terminator is reached. Intitiation, therefore, involves the recognition of a promotor sequence and the unzipping of a section of DNA under the influence of transcription factors and RNA polymerases.
Elongation
The next phase in the transcription process is elongation. With
the coded sequence exposed, RNAPs can read each individual
adenine, guanine, cytosine, or thymine base on the template
strand and connect the correct partner base to it. It is
important to remember that RNA is unable to replicate thymine
and replaces this with the nucleobase known as uracil.
If, for example, a short DNA sequence on the template strand is
represented by C-A-G-T-T-A or
cytosine-adenine-guanine-thymine-thymine-adenine, RNAP will
connect the correct partner bases obtained from populations of
free-floating bases within the nucleus. In this example, RNA
polymerase will attach a guanine base to cytosine, uracil to
adenine, cytosine to guanine, and adenine to thymine to form a
strand of messenger RNA with the coded nitrogenous base sequence
G-U-C-A-A-U. This process repeats until the RNAP enzyme detects
a sequence of genetic code that terminates it – the terminator.
The next phase in the transcription process is elongation. With the coded sequence exposed, RNAPs can read each individual adenine, guanine, cytosine, or thymine base on the template strand and connect the correct partner base to it. It is important to remember that RNA is unable to replicate thymine and replaces this with the nucleobase known as uracil.
If, for example, a short DNA sequence on the template strand is represented by C-A-G-T-T-A or cytosine-adenine-guanine-thymine-thymine-adenine, RNAP will connect the correct partner bases obtained from populations of free-floating bases within the nucleus. In this example, RNA polymerase will attach a guanine base to cytosine, uracil to adenine, cytosine to guanine, and adenine to thymine to form a strand of messenger RNA with the coded nitrogenous base sequence G-U-C-A-A-U. This process repeats until the RNAP enzyme detects a sequence of genetic code that terminates it – the terminator.
Termination
When the RNAPs detect a terminator sequence, the final phase of
transcription – termination – takes place. The string of RNAPs
disconnect from the DNA and the result is a strand of messenger
RNA. This mRNA carries the code that will eventually instruct
tRNA which amino acids to bring to a ribosome.
Messenger RNA leaves the nucleus via nuclear pores primarily
through diffusion but sometimes needs help from transporter enzymes and ATP
to reach its destination.
When the RNAPs detect a terminator sequence, the final phase of transcription – termination – takes place. The string of RNAPs disconnect from the DNA and the result is a strand of messenger RNA. This mRNA carries the code that will eventually instruct tRNA which amino acids to bring to a ribosome.
Messenger RNA leaves the nucleus via nuclear pores primarily through diffusion but sometimes needs help from transporter enzymes and ATP to reach its destination.
Translation Process in Protein Synthesis
During the translation process, the small and large subunits of
a ribosome close over a strand of mRNA, trapping it loosely
inside. Ribosomes arrange the strand into codons or sets of
three nitrogenous base letters. This is because the code for a
single amino acid – the most basic form of a protein – is a
three-letter nucleobase code.
As ribosomes recognize parts of code, we can say they understand
it. The jumble of copied letters made during the transcription
phase can be read and understood in the translation phase.
For example, GGU, GGC, GGA, and GGG code for the amino acid
known as glycine. Most amino acids have multiple codes as this
lowers the chance of mistakes – if RNA polymerase accidently
connects adenine instead of cytosine to GG, it doesn’t matter.
Both GGC and GGA code for the same amino acid. You can see a list of mRNA codons for the twenty non-essential amino
acids here.
There is only one start codon code – AUG. Three codons –
TAA, TAG, and TGA – represent stop codons. Neither start nor
stop codons match the code for an amino acid; they are
non-coding. The single start and three stop codons are clearly
marked on this codon wheel.
When a codon becomes visible – once the previous codon has been
linked to an amino acid – a section of a transfer RNA molecule
fits into the mRNA codon. This ‘key’ is called the anticodon.
Transfer RNA has two roles – to attach to an amino acid outside
of the ribosome and to deploy this amino acid at the right time
and in the right position on an mRNA strand within the ribosome.
Tens to thousands of transfer RNA molecules produce a
polypeptide chain. Titin or connectin is the largest protein
molecule and contains around 33,000 amino acids. The smallest
functional polypeptide is glutathione – just three amino acids.
To produce glutathione, first the ribosome and tRNA must read
the start codon (three bases), then read the first
protein-coding codon (three bases), the second (three bases),
the third (three bases), and the stop codon (three bases). The
coding DNA and mRNA recipes (sequences) for glutathione contain
nine bases. There may or may not be additional sections of
non-coding DNA within this recipe. Non-coding sequences do not produce amino acids.
As with the process of transcription, translation within the
ribosome is also split into the three stages of initiation,
elongation, and termination.
Initiation involves the recognition by the ribosome of the mRNA
start codon. Elongation refers to the process whereby the
ribosome moves along the mRNA transcript, recognizing and
exposing individual codons so that tRNA can bring the right
amino acids. The anticodon arm of tRNA attaches to the
appropriate mRNA codon under the influence of ribosomal enzymes.
Finally, termination occurs when the ribosome recognizes the
mRNA stop codon; the completed polypeptide chain is then
released into the cytoplasm. It is sent wherever it is needed –
inside the cell or to other tissues, exiting the cell membrane via exocytosis.
https://biologydictionary.net/protein-synthesis/
5.6 Protein Synthesis
Protein Synthesis
During the translation process, the small and large subunits of a ribosome close over a strand of mRNA, trapping it loosely inside. Ribosomes arrange the strand into codons or sets of three nitrogenous base letters. This is because the code for a single amino acid – the most basic form of a protein – is a three-letter nucleobase code.
As ribosomes recognize parts of code, we can say they understand it. The jumble of copied letters made during the transcription phase can be read and understood in the translation phase.
For example, GGU, GGC, GGA, and GGG code for the amino acid known as glycine. Most amino acids have multiple codes as this lowers the chance of mistakes – if RNA polymerase accidently connects adenine instead of cytosine to GG, it doesn’t matter. Both GGC and GGA code for the same amino acid. You can see a list of mRNA codons for the twenty non-essential amino acids here.
There is only one start codon code – AUG. Three codons – TAA, TAG, and TGA – represent stop codons. Neither start nor stop codons match the code for an amino acid; they are non-coding. The single start and three stop codons are clearly marked on this codon wheel.
When a codon becomes visible – once the previous codon has been linked to an amino acid – a section of a transfer RNA molecule fits into the mRNA codon. This ‘key’ is called the anticodon. Transfer RNA has two roles – to attach to an amino acid outside of the ribosome and to deploy this amino acid at the right time and in the right position on an mRNA strand within the ribosome.
Tens to thousands of transfer RNA molecules produce a polypeptide chain. Titin or connectin is the largest protein molecule and contains around 33,000 amino acids. The smallest functional polypeptide is glutathione – just three amino acids. To produce glutathione, first the ribosome and tRNA must read the start codon (three bases), then read the first protein-coding codon (three bases), the second (three bases), the third (three bases), and the stop codon (three bases). The coding DNA and mRNA recipes (sequences) for glutathione contain nine bases. There may or may not be additional sections of non-coding DNA within this recipe. Non-coding sequences do not produce amino acids.
As with the process of transcription, translation within the ribosome is also split into the three stages of initiation, elongation, and termination.
Initiation involves the recognition by the ribosome of the mRNA start codon. Elongation refers to the process whereby the ribosome moves along the mRNA transcript, recognizing and exposing individual codons so that tRNA can bring the right amino acids. The anticodon arm of tRNA attaches to the appropriate mRNA codon under the influence of ribosomal enzymes.
Finally, termination occurs when the ribosome recognizes the mRNA stop codon; the completed polypeptide chain is then released into the cytoplasm. It is sent wherever it is needed – inside the cell or to other tissues, exiting the cell membrane via exocytosis.
The Art of Protein Synthesis
Transcription
Summary
Review
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Protein Synthesis
Learning Objectives
By the end of this section, you will be able to:
- Explain how the genetic code stored within DNA determines the protein that will form
- Describe the process of transcription
- Describe the process of translation
- Discuss the function of ribosomes
It was mentioned earlier that DNA provides a “blueprint” for the cell structure and physiology. This refers to the fact that DNA contains the information necessary for the cell to build one very important type of molecule: the protein. Most structural components of the cell are made up, at least in part, by proteins and virtually all the functions that a cell carries out are completed with the help of proteins. One of the most important classes of proteins is enzymes, which help speed up necessary biochemical reactions that take place inside the cell. Some of these critical biochemical reactions include building larger molecules from smaller components (such as occurs during DNA replication or synthesis of microtubules) and breaking down larger molecules into smaller components (such as when harvesting chemical energy from nutrient molecules). Whatever the cellular process may be, it is almost sure to involve proteins. Just as the cell’s genome describes its full complement of DNA, a cell’s proteome is its full complement of proteins. Protein synthesis begins with genes. A gene is a functional segment of DNA that provides the genetic information necessary to build a protein. Each particular gene provides the code necessary to construct a particular protein. Gene expression, which transforms the information coded in a gene to a final gene product, ultimately dictates the structure and function of a cell by determining which proteins are made.
The interpretation of genes works in the following way. Recall that proteins are polymers, or chains, of many amino acid building blocks. The sequence of bases in a gene (that is, its sequence of A, T, C, G nucleotides) translates to an amino acid sequence. A triplet is a section of three DNA bases in a row that codes for a specific amino acid. Similar to the way in which the three-letter code d-o-g signals the image of a dog, the three-letter DNA base code signals the use of a particular amino acid. For example, the DNA triplet CAC (cytosine, adenine, and cytosine) specifies the amino acid valine. Therefore, a gene, which is composed of multiple triplets in a unique sequence, provides the code to build an entire protein, with multiple amino acids in the proper sequence ((Figure)). The mechanism by which cells turn the DNA code into a protein product is a two-step process, with an RNA molecule as the intermediate.
From DNA to RNA: Transcription
DNA is housed within the nucleus, and protein synthesis takes place in the cytoplasm, thus there must be some sort of intermediate messenger that leaves the nucleus and manages protein synthesis. This intermediate messenger is messenger RNA (mRNA), a single-stranded nucleic acid that carries a copy of the genetic code for a single gene out of the nucleus and into the cytoplasm where it is used to produce proteins.
There are several different types of RNA, each having different functions in the cell. The structure of RNA is similar to DNA with a few small exceptions. For one thing, unlike DNA, most types of RNA, including mRNA, are single-stranded and contain no complementary strand. Second, the ribose sugar in RNA contains an additional oxygen atom compared with DNA. Finally, instead of the base thymine, RNA contains the base uracil. This means that adenine will always pair up with uracil during the protein synthesis process.
Gene expression begins with the process called transcription, which is the synthesis of a strand of mRNA that is complementary to the gene of interest. This process is called transcription because the mRNA is like a transcript, or copy, of the gene’s DNA code. Transcription begins in a fashion somewhat like DNA replication, in that a region of DNA unwinds and the two strands separate, however, only that small portion of the DNA will be split apart. The triplets within the gene on this section of the DNA molecule are used as the template to transcribe the complementary strand of RNA ((Figure)). A codon is a three-base sequence of mRNA, so-called because they directly encode amino acids. Like DNA replication, there are three stages to transcription: initiation, elongation, and termination.
Stage 1: Initiation. A region at the beginning of the gene called a promoter—a particular sequence of nucleotides—triggers the start of transcription.
Stage 2: Elongation. Transcription starts when RNA polymerase unwinds the DNA segment. One strand, referred to as the coding strand, becomes the template with the genes to be coded. The polymerase then aligns the correct nucleic acid (A, C, G, or U) with its complementary base on the coding strand of DNA. RNA polymerase is an enzyme that adds new nucleotides to a growing strand of RNA. This process builds a strand of mRNA.
Stage 3: Termination. When the polymerase has reached the end of the gene, one of three specific triplets (UAA, UAG, or UGA) codes a “stop” signal, which triggers the enzymes to terminate transcription and release the mRNA transcript.
Before the mRNA molecule leaves the nucleus and proceeds to protein synthesis, it is modified in a number of ways. For this reason, it is often called a pre-mRNA at this stage. For example, your DNA, and thus complementary mRNA, contains long regions called non-coding regions that do not code for amino acids. Their function is still a mystery, but the process called splicing removes these non-coding regions from the pre-mRNA transcript ((Figure)). A spliceosome—a structure composed of various proteins and other molecules—attaches to the mRNA and “splices” or cuts out the non-coding regions. The removed segment of the transcript is called an intron. The remaining exons are pasted together. An exon is a segment of RNA that remains after splicing. Interestingly, some introns that are removed from mRNA are not always non-coding. When different coding regions of mRNA are spliced out, different variations of the protein will eventually result, with differences in structure and function. This process results in a much larger variety of possible proteins and protein functions. When the mRNA transcript is ready, it travels out of the nucleus and into the cytoplasm.
From RNA to Protein: Translation
Like translating a book from one language into another, the codons on a strand of mRNA must be translated into the amino acid alphabet of proteins. Translation is the process of synthesizing a chain of amino acids called a polypeptide. Translation requires two major aids: first, a “translator,” the molecule that will conduct the translation, and second, a substrate on which the mRNA strand is translated into a new protein, like the translator’s “desk.” Both of these requirements are fulfilled by other types of RNA. The substrate on which translation takes place is the ribosome.
Remember that many of a cell’s ribosomes are found associated with the rough ER, and carry out the synthesis of proteins destined for the Golgi apparatus. Ribosomal RNA (rRNA) is a type of RNA that, together with proteins, composes the structure of the ribosome. Ribosomes exist in the cytoplasm as two distinct components, a small and a large subunit. When an mRNA molecule is ready to be translated, the two subunits come together and attach to the mRNA. The ribosome provides a substrate for translation, bringing together and aligning the mRNA molecule with the molecular “translators” that must decipher its code.
The other major requirement for protein synthesis is the translator molecules that physically “read” the mRNA codons. Transfer RNA (tRNA) is a type of RNA that ferries the appropriate corresponding amino acids to the ribosome, and attaches each new amino acid to the last, building the polypeptide chain one-by-one. Thus tRNA transfers specific amino acids from the cytoplasm to a growing polypeptide. The tRNA molecules must be able to recognize the codons on mRNA and match them with the correct amino acid. The tRNA is modified for this function. On one end of its structure is a binding site for a specific amino acid. On the other end is a base sequence that matches the codon specifying its particular amino acid. This sequence of three bases on the tRNA molecule is called an anticodon. For example, a tRNA responsible for shuttling the amino acid glycine contains a binding site for glycine on one end. On the other end it contains an anticodon that complements the glycine codon (GGA is a codon for glycine, and so the tRNAs anticodon would read CCU). Equipped with its particular cargo and matching anticodon, a tRNA molecule can read its recognized mRNA codon and bring the corresponding amino acid to the growing chain ((Figure)).
Much like the processes of DNA replication and transcription, translation consists of three main stages: initiation, elongation, and termination. Initiation takes place with the binding of a ribosome to an mRNA transcript. The elongation stage involves the recognition of a tRNA anticodon with the next mRNA codon in the sequence. Once the anticodon and codon sequences are bound (remember, they are complementary base pairs), the tRNA presents its amino acid cargo and the growing polypeptide strand is attached to this next amino acid. This attachment takes place with the assistance of various enzymes and requires energy. The tRNA molecule then releases the mRNA strand, the mRNA strand shifts one codon over in the ribosome, and the next appropriate tRNA arrives with its matching anticodon. This process continues until the final codon on the mRNA is reached which provides a “stop” message that signals termination of translation and triggers the release of the complete, newly synthesized protein. Thus, a gene within the DNA molecule is transcribed into mRNA, which is then translated into a protein product ((Figure)).
Commonly, an mRNA transcription will be translated simultaneously by several adjacent ribosomes. This increases the efficiency of protein synthesis. A single ribosome might translate an mRNA molecule in approximately one minute; so multiple ribosomes aboard a single transcript could produce multiple times the number of the same protein in the same minute. A polyribosome is a string of ribosomes translating a single mRNA strand.
Watch this video to learn about ribosomes. The ribosome binds to the mRNA molecule to start translation of its code into a protein. What happens to the small and large ribosomal subunits at the end of translation?
Chapter Review
DNA stores the information necessary for instructing the cell to perform all of its functions. Cells use the genetic code stored within DNA to build proteins, which ultimately determine the structure and function of the cell. This genetic code lies in the particular sequence of nucleotides that make up each gene along the DNA molecule. To “read” this code, the cell must perform two sequential steps. In the first step, transcription, the DNA code is converted into a RNA code. A molecule of messenger RNA that is complementary to a specific gene is synthesized in a process similar to DNA replication. The molecule of mRNA provides the code to synthesize a protein. In the process of translation, the mRNA attaches to a ribosome. Next, tRNA molecules shuttle the appropriate amino acids to the ribosome, one-by-one, coded by sequential triplet codons on the mRNA, until the protein is fully synthesized. When completed, the mRNA detaches from the ribosome, and the protein is released. Typically, multiple ribosomes attach to a single mRNA molecule at once such that multiple proteins can be manufactured from the mRNA concurrently.
Interactive Link Questions
Watch this video to learn about ribosomes. The ribosome binds to the mRNA molecule to start translation of its code into a protein. What happens to the small and large ribosomal subunits at the end of translation?
They separate and move and are free to join translation of other segments of mRNA.
Review Questions
Which of the following is not a difference between DNA and RNA?
- DNA contains thymine whereas RNA contains uracil
- DNA contains deoxyribose and RNA contains ribose
- DNA contains alternating sugar-phosphate molecules whereas RNA does not contain sugars
- RNA is single stranded and DNA is double stranded
C
Transcription and translation take place in the ________ and ________, respectively.
- nucleus; cytoplasm
- nucleolus; nucleus
- nucleolus; cytoplasm
- cytoplasm; nucleus
A
How many “letters” of an RNA molecule, in sequence, does it take to provide the code for a single amino acid?
- 1
- 2
- 3
- 4
C
Which of the following is not made out of RNA?
- the carriers that shuffle amino acids to a growing polypeptide strand
- the ribosome
- the messenger molecule that provides the code for protein synthesis
- the intron
B
Critical Thinking Questions
Briefly explain the similarities between transcription and DNA replication.
Transcription and DNA replication both involve the synthesis of nucleic acids. These processes share many common features—particularly, the similar processes of initiation, elongation, and termination. In both cases the DNA molecule must be untwisted and separated, and the coding (i.e., sense) strand will be used as a template. Also, polymerases serve to add nucleotides to the growing DNA or mRNA strand. Both processes are signaled to terminate when completed.
Contrast transcription and translation. Name at least three differences between the two processes.
Transcription is really a “copy” process and translation is really an “interpretation” process, because transcription involves copying the DNA message into a very similar RNA message whereas translation involves converting the RNA message into the very different amino acid message. The two processes also differ in their location: transcription occurs in the nucleus and translation in the cytoplasm. The mechanisms by which the two processes are performed are also completely different: transcription utilizes polymerase enzymes to build mRNA whereas translation utilizes different kinds of RNA to build protein.
Glossary
- anticodon
- consecutive sequence of three nucleotides on a tRNA molecule that is complementary to a specific codon on an mRNA molecule
- codon
- consecutive sequence of three nucleotides on an mRNA molecule that corresponds to a specific amino acid
- exon
- one of the coding regions of an mRNA molecule that remain after splicing
- gene
- functional length of DNA that provides the genetic information necessary to build a protein
- gene expression
- active interpretation of the information coded in a gene to produce a functional gene product
- intron
- non-coding regions of a pre-mRNA transcript that may be removed during splicing
- messenger RNA (mRNA)
- nucleotide molecule that serves as an intermediate in the genetic code between DNA and protein
- polypeptide
- chain of amino acids linked by peptide bonds
- polyribosome
- simultaneous translation of a single mRNA transcript by multiple ribosomes
- promoter
- region of DNA that signals transcription to begin at that site within the gene
- proteome
- full complement of proteins produced by a cell (determined by the cell’s specific gene expression)
- ribosomal RNA (rRNA)
- RNA that makes up the subunits of a ribosome
- RNA polymerase
- enzyme that unwinds DNA and then adds new nucleotides to a growing strand of RNA for the transcription phase of protein synthesis
- spliceosome
- complex of enzymes that serves to splice out the introns of a pre-mRNA transcript
- splicing
- the process of modifying a pre-mRNA transcript by removing certain, typically non-coding, regions
- transcription
- process of producing an mRNA molecule that is complementary to a particular gene of DNA
- transfer RNA (tRNA)
- molecules of RNA that serve to bring amino acids to a growing polypeptide strand and properly place them into the sequence
- translation
- process of producing a protein from the nucleotide sequence code of an mRNA transcript
- triplet
- consecutive sequence of three nucleotides on a DNA molecule that, when transcribed into an mRNA codon, corresponds to a particular amino acid