Peptide bonds are a specific type of link between one amino acid and another, which takes place through an amino group (-NH 2 ) in the first amino acid and a carboxyl group (-COOH) in the second, producing a covalent bond – CO-NH- and releasing a water molecule. For example oxytocin, vasopressin, and leptin.
In this way, a new molecule called peptide is obtained, which will bear the name of both amino acids. The peptide bond between an alanine molecule (providing the -NH 2 terminal ) and a serine molecule ( providing the -COOH terminal) is named an alanyl-serine peptide.
This is one of the forms of bonding that allows amino acids to be joined (by dehydration) to produce more complex structures (polypeptides) since once the bond is obtained, it is possible to continue joining amino acids through the same process, starting from the terminal carboxyl group. In this same way, more complex structures such as polypeptides and proteins can be obtained. It is an extremely common procedure in living beings.
Peptide bonds have certain characteristics. For example, the bond established is of a simple but shorter type: with characteristics of a double bond, such as being stabilized by resonance. The latter prevents free turns around the bond (something common in this type of bond), which gives the peptide bond an unavoidable planar structure.
Similarly, peptide bonds can be degraded or broken by hydrolysis (addition of water), releasing an amount of energy in a very slow process. This process can be accelerated in the presence of acidic, basic or enzymatic catalysts.
Any peptide is a perfect example of peptide bonds, as they are the result of this type of joining of amino acids. Here are some of the most important:
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