Dipeptide

A dipeptide is an

Dipeptides are white solids. Many are far more water-soluble than the parent amino acids.^[1] For example, the dipeptide Ala-Gln has the solubility of 586 g/L more than 10x the solubility of Gln (35 g/L). Dipeptides also can exhibit different stabilities, e.g. with respect to hydrolysis. Gln does not withstand sterilization procedures, whereas this dipeptide does. Because dipeptides are prone to hydrolysis, the high solubility is exploited in infusions, i.e. to provide nutrition.^[2]

Examples

Commercial value

About six dipeptides are of commercial interest.^[1]

• Aspartame (N-L-α-aspartyl-L-phenylalanine 1-methyl ester) is an artificial sweetener.
• Carnosine (beta-alanyl-L-histidine) and Anserine (beta-alanyl-N-methyl histidine) are highly concentrated in muscle and brain tissues. They are used in sports medicines.
• Acetylcarnosine, cataract prevention
• Ala-Gln and Gly-Tyr, infusion^[2]
• Val-Tyr, antihypertensive

Other dipeptides

• Homoanserine (N-(4-aminobutyryl)-L-histidine) is another dipeptide identified in the brain and muscles of mammals.
• Diphenylalanine is the most studied building block in peptide nanotechnology
• neuroactive dipeptide
  which plays a role in pain regulation in the brain.
• Balenine [ja] (or ophidine) (beta-alanyl-N tau-methyl histidine) has been identified in the muscles of several species of mammal (including man), and the chicken.
• Polysphondylium violaceum
  .
• marine sponge
  Geodia barretti.
• Pseudoproline
• Dialanine is commonly used as a model in molecular dynamics.
• Xenortides, isolated from the bacterium Xenorhabdus nematophila

Production

Synthetic dipeptides

Dipeptides are produced by coupling amino acids. The amino group on one amino acid is rendered non-nucleophilic (P in eq) and the carboxylic acid group in the second amino acid is deactivated as its methyl ester. The two modified amino acids are then combined in the presence of a coupling agent, which facilitates formation of the amide bond:

RCH(NHP)CO₂H + R'CH(NH₂)CO₂CH₃ → RCH(NHP)C(O)NH(CHR')CO₂CH₃ + H₂O

Subsequent to this coupling reaction, the amine protecting group P and the ester are converted to the free amine and carboxylic acid, respectively.^[3]

For many amino acids, the ancillary functional groups are protected. The condensation of the amine and the carboxylic acid to form the peptide bond generally employs coupling agents to activate the carboxylic acid.^[4]

The Bergmann azlactone peptide synthesis is a classic organic synthesis for the preparation of dipeptides.^[1]

Biosynthesis

Dipeptides are produced from

Diketopiperazines are a special class of dipeptides, which are cyclic. They form as side products in peptide synthesis. Many have been produced from non-canonical amino acids.^[7]