Substrate channeling

Substrate channeling is the passing of the intermediary metabolic product of one enzyme directly to another enzyme or active site without its release into solution. When several consecutive enzymes of a metabolic pathway channel substrates between themselves, this is called a metabolon. Channeling can make a metabolic pathway more rapid and efficient than it would be if the enzymes were randomly distributed in the cytosol, or prevent the release of unstable intermediates.[1] It can also protect an intermediate from being consumed by competing reactions catalyzed by other enzymes.

Channeling can occur in several ways. One possibility, which occurs in the pyruvate dehydrogenase complex, is by a substrate being attached to a flexible arm that moves between several active sites (not very likely).[2] Another possibility is by two active sites being connected by a tunnel through the protein and the substrate moving through the tunnel; this is seen in tryptophan synthase.[1] A third possibility is by a charged region on the surface of the enzyme acting as a pathway or "electrostatic highway" to guide a substrate that has the opposite charge from one active site to another. This is seen in the bifunctional enzyme dihydrofolate reductase-thymidylate synthase.[3] The channeling of aminoacyl-tRNA for protein synthesis in vivo has been also reported.[4] The channeling via transient protein-protein interaction was reported between NAD(H) depend dehydrogenases in regulation of aerobic and anaerobic glycolysis.[5]

A presence of channel in enzyme structure is rather common feature as more than 68% of enzymes have active site access channels.[6] Enzyme channels can be identified and characterized by MOLEonline software.

See also

References

  1. Huang X, Holden HM, Raushel FM (2001). "Channeling of substrates and intermediates in enzyme-catalyzed reactions". Annu. Rev. Biochem. 70: 149–80. doi:10.1146/annurev.biochem.70.1.149. PMID 11395405.
  2. Perham RN (2000). "Swinging arms and swinging domains in multifunctional enzymes: catalytic machines for multistep reactions". Annu. Rev. Biochem. 69: 961–1004. doi:10.1146/annurev.biochem.69.1.961. PMID 10966480.
  3. Miles EW, Rhee S, Davies DR (April 1999). "The molecular basis of substrate channeling". J. Biol. Chem. 274 (18): 12193–6. doi:10.1074/jbc.274.18.12193. PMID 10212181.
  4. Negrutskii B.S.; Deutscher M.P. (1991). "Channeling of aminoacyl-tRNA for protein synthesis in vivo". Proc. Natl. Acad. Sci. USA. 88 (11): 4991–5. doi:10.1073/pnas.88.11.4991. PMC 51793. PMID 2052582.
  5. Svedružić Ž.M.; Odorčić I.; Chang C.H.; Svedružić D. (2020). "Substrate Channeling via a Transient Protein-Protein Complex: The case of D-Glyceraldehyde-3-Phosphate Dehydrogenase and L-Lactate Dehydrogenase". Sci. Rep. 10 (10): 10404. doi:10.1038/s41598-020-67079-2. PMC 7320145. PMID 32591631.
  6. Pravda L.; Berka K.; Svobodova Varekova R; Banas P.; Laskowski R.A.; Koca J.; Otyepka M. (2014). "Anatomy of Enzyme Channels". BMC Bioinformatics. 15: 379. doi:10.1186/s12859-014-0379-x. PMC 4245731. PMID 25403510.
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