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Chemistry LibreTexts

26.5: Peptides

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  • Page ID
    54019
  • Cells in our bodies have an intricate mechanism for the manufacture of proteins. Humans have to use other techniques in order to synthesize the same proteins in a lab. The chemistry of peptide synthesis is complicated. Both active groups on an amino acid can react and the amino acid sequence must be a specific one in order for the protein to function. Robert Merrifield developed the first synthetic approach for making proteins in the lab, a manual approach which was lengthy and tedious (and, he won the Nobel Prize in Chemistry in 1984 for his work). Today however, automated systems can crank out a peptide in a very short period of time.

    Peptides

    peptide is a combination of amino acids in which the amine group of one amino acid has undergone a reaction with the carboxyl group of another amino acid. The reaction is a condensation reaction, forming an amide group \(\left( \ce{CO-N} \right)\), shown below.

    Condensation reaction of two amino acids to form a peptide

    Figure 26.5.1: Amino acids join together to form a molecule called a dipeptide. The \(\ce{C-N}\) bond is called a peptide bond. The order of amino acids is by convention shown with the free amine group on the left and the free carboxyl group on the right.

    peptide bond is the amide bond that occurs between the amine nitrogen of one amino acid and the carboxyl carbon of another amino acid. The resulting molecule is called a dipeptide. Notice that the particular side chains of each amino acid are irrelevant since the \(\ce{R}\) groups are not involved in the peptide bond.

    The dipeptide has a free amine group on one end of the molecule and a free carboxyl group on the other end. Each is capable of extending the chain through the formation of another peptide bond. The particular sequence of amino acids in a longer chain is called an amino acid sequence. By convention, the amino acid sequence is listed in the order such that the free amine group is on the left end of the molecule and the free carboxyl group is on the right end of the molecule. For example, suppose that a sequence of the amino acids glycine, tryptophan, and alanine is formed with the free amine group as part of the glycine and the free carboxyl group as part of the alanine. The amino acid sequence can be easily written using the abbreviations as Gyl-Trp-Ala. This is a different sequence from Ala-Trp-Gly because the free amine and carboxyl groups would be on different amino acids in that case.

    Contributors

    • CK-12 Foundation by Sharon Bewick, Richard Parsons, Therese Forsythe, Shonna Robinson, and Jean Dupon.