11.2: Introduction to Amino Acids and Proteins (2025)

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    Proteins are polymers of amino acids, linked by amide groups known as peptide bonds. An amino acid can be thought of as having two components: a 'backbone', or 'main chain', composed of an ammonium group (H3N+-C), an 'alpha-carbon' bonded to the nitrogen atom, a carboxylate(COO-), and a variable 'side chain' (in green below) bonded to the alpha-carbon (Figure \(\PageIndex{1}\)).

    11.2: Introduction to Amino Acids and Proteins (2)

    (Figure \(\PageIndex{1}\)). Structures of amino acids.

    There are twenty different side chains in naturally occurring amino acids, and it is the identity of the side chain that determines the identity of the amino acid: for example, if the side chain is a -CH3 group, the amino acid is alanine, and if the side chain is a -CH2OH group, the amino acid is serine. Many amino acid side chains contain a functional group (the side chain of serine, for example, contains a primary alcohol), while others, like alanine, lack a functional group, and contain only a simple hydrocarbon group.

    The two 'hooks' on an amino acid monomer are the ammoniumand carboxylate groups. Proteins (polymers of ~50 amino acids or more) and peptides (shorter polymers) are formed when the amino group of one amino acid monomer reacts with the carboxylate carbon of another amino acid to form an amide linkage, which in protein terminology is a peptide bond. Which amino acids are linked, and in what order - the protein sequence - is what distinguishes one protein from another.This sequence is coded for by an organism's DNA. Protein sequences are written in the ammoniumterminal (N-terminal) to carboxylate terminal (C-terminal) direction, with either three-letter or single-letter abbreviations for the amino acids. Below is a four amino acid peptide with the sequence "cysteine - histidine - glutamate - methionine". Using the single-letter code, the sequence is abbreviated CHEM (Figure \(\PageIndex{2}\)).

    11.2: Introduction to Amino Acids and Proteins (3)

    Figure \(\PageIndex{2}\). The CHEM peptide.

    When an amino acid is incorporated into a protein it loses a molecule of water and what remains is called a residue of the original amino acid. Thus we might refer to the 'glutamate residue' at position 3 of the CHEM peptide above.

    Once a protein polymer is constructed, it in many cases folds up very specifically into a three-dimensional structure, which often includes one or more 'binding pockets' in which other molecules can be bound. It is this shape of this folded structure, and the precise arrangement of the functional groups within the structure (especially in the area of the binding pocket) that determines the function of the protein.

    Enzymes are proteins which catalyze biochemical reactions. One or more reacting molecules - often called substrates - become bound in the active site pocket of an enzyme, where the actual reaction takes place. Receptors are proteins that bind specifically to one or more molecules - referred to as ligands - to initiate a biochemical process. For example, we saw in the introduction to this chapter that the TrpVI receptor in mammalian tissues binds capsaicin (from hot chili peppers) in its binding pocket and initiates a heat/pain signal which is sent to the brain.

    Contributors and Attributions

    • Organic Chemistry With a Biological Emphasis byTim Soderberg(University of Minnesota, Morris)
    11.2: Introduction to Amino Acids and Proteins (2025)

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