Proteins are by far the most important macromolecule within the body.
What? Proteins are just muscles, aren’t they?
Yes and no. All muscles are made up of proteins, but, by no means are all proteins muscles. The only function of DNA is to synthesise or control the synthesis of proteins. Ultimately, this means that proteins must be able to undertake, or at the very least have a hand in, every biochemical task the human body needs to operate. Proteins, therefore, not only act as muscles to contract and manipulate the skeleton, but also enzymes, receptors and even hormones. By focusing on DNA replication, you can appreciate the number of enzymes that are involved in just one single process. With each of these enzymes consisting of proteins, and each enzyme being dependent on its shape to function, it is clear that synthesising the correct proteins is vitally important.
Proteins are made up of a single repeating unit, known as an amino acid. Amino acids follow the same general formula, but each have a different side chain (known by convention as the R group) shown in figure 1, which gives each amino acid varying properties. These amino acids are joined together (in a rather complicated process discussed below) forming a peptide bond. The amino acids then interact and fold in a manner specific to their structure in order to form the complete protein. The function of the finished protein is usually very dependent on the structure of the protein. The sequence of amino acids in the protein determines this structure and therefore function, due to the interaction of R groups within the protein. An accidental change in the amino acid order can dramatically alter protein structure and function, causing the protein to become useless or to cause disease.
figure 1. General formula for an amino acid
As seen in figure 2 below, the properties of each amino acid depends on their side chains.
figure 2. Labelled amino acids
It is all to do with the sequence of DNA bases. DNA has four potential bases, adenine (A), thymine (T), guanine (G) and cytosine (C). Eeach sequence of three consecutive bases, referred to as a codon, codes for one amino acid. Thus, the specific sequence of bases codes for the specific sequence of amino acids, which determines the structure of the protein. A simple concept, yet difficult for the body to execute. This is because DNA is not able to leave the nucleus, but proteins are made in the cytoplasm, outside the nucleus.
Via RNA! This is a molecule very similar to DNA, with three major differences.
Within the nucleus DNA is unwound using an enzyme known as DNA helicase. Then a strand of RNA is made from the template of the DNA strand which contains the protein code. This RNA is called messenger RNA (mRNA). The process of using a DNA template to make RNA is known as transcription. It uses the enzyme RNA polymerase to assemble to correct RNA nucleotides (due to the complementary base pairing of bases between DNA and RNA strands) and then bonds the nucleotides together. This is very similar to the DNA polymerase enzyme used in DNA replication. Transcription is summarised below.
The mRNA transcript then travels out of the nucleus and reaches a ribosome, the site of protein synthesis. At the ribosome, the sequence of codons on the mRNA is read by feeding mRNA through the ribosome, and amino acids are brought in and attached according to this sequence. This process is known as translation. The mechanism of translation is rather complicated (and too long for this article), but is summarised in figure 5 below.
Finally, you will be relieved to know, we have constructed a working protein! All that needs to occur now is the folding of the protein into its final structure. Fortunately for us, this occurs simply due to the structure of the protein and doesn’t require any specialised enzymes.
It is important to understand biochemical process like protein synthesis for many reasons. Firstly, if these processes malfunction then many disease can occur. A mutation of a single base can potentially change the order of amino acids within a protein, resulting in disease. This is the case with sickle cell anaemia, where the substitution of just one of the bases in the DNA code causes a glutamic acid to be swapped with a valine, with devastating consequences. Secondly, by understanding these processes, it may be possible to manipulate them with drugs to target specific diseases or pathogens that do not synthesise proteins using the same enzymes or processes.
References:
http://www.proteinsynthesis.org/what-is-protein-synthesis/
http://chemistry.elmhurst.edu/vchembook/584proteinsyn.html
http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-21/CB21.html
http://www.mun.ca/biology/desmid/brian/BIOL2060/BIOL2060-22/CB22.html
