Metabolon
In biochemistry, a metabolon is a temporary structural-functional complex formed between sequential enzymes of a metabolic pathway, held together both by non-covalent interactions and by structural elements of the cell, such as integral membrane proteins and proteins of the cytoskeleton.
The formation of metabolons allows the intermediate product from one enzyme to be passed
History
The concept of structural-metabolic cellular complexes was first conceived in 1970 by A. M. Kuzin of the USSR Academy of Sciences,[4] and adopted in 1972 by Paul A. Srere of the University of Texas for the enzymes of the citric acid cycle.[5] This hypothesis was well accepted in the former USSR and further developed for the complex of glycolytic enzymes (Embden-Meyerhof-Parnas pathway) by B.I. Kurganov and A.E. Lyubarev.[6][7][8][9] In the mid-1970s, the group of F.M. Clarke at the University of Queensland, Australia also worked on the concept.[10][11] The name "metabolon" was first proposed in 1985 by Paul Srere[12] during a lecture in Debrecen, Hungary.[13]
The case of Fatty Acid Synthesis
In
Examples
Metabolic pathways in which formation of metabolons occurs | |||||
---|---|---|---|---|---|
Metabolic pathway | Events supporting metabolon's formation | ||||
DNA biosynthesis | A, B, C, E, F | ||||
RNA biosynthesis |
A, B, C, E, F | ||||
Protein biosynthesis | A, B, C, D, E | ||||
Glycogen biosynthesis | C, E | ||||
Pyrimidine biosynthesis | A, C, D, F | ||||
Purine biosynthesis | A, E | ||||
Lipid biosynthesis | A, B, C, H | ||||
Steroid biosynthesis | A, C, E | ||||
Metabolism of amino acids | A, B, D, H | ||||
Glycolysis | A, B, C, D, I | ||||
Citric acid cycle | B, C, D, E, G | ||||
Fatty acids oxidation | A, B, C, D | ||||
Electron transport chain | C, I | ||||
Antibiotic biosynthesis | A, E | ||||
Urea cycle | B, D | ||||
cAMP degradation | A, D, E | ||||
A – Channeling, B – Specific protein-protein interactions, C – Specific protein – membrane interactions, D – Kinetic effects, E – Multienzyme complexes identified, F – Genetic proofs, G – Operative modeled systems, H – Identified multifunctional proteins, I – Physico-chemical proofs.[15] |
See also
References
- PMID 25537779.
- PMID 28508886.
- S2CID 19187608.
- ^ Kuzin A. M. Structural – metabolic hypothesis in radiobiology. Moscow: Nauka Ed., 1970.- 50 p.
- ^ Srere P. A. Is there an organization of Krebs cycle enzymes in the mitochondrial matrix? In: Energy Metabolism and the Regulation of Metabolic Processes in Mitochondria, R. W. Hanson and W.A. Mehlman (Eds.). New York: Academic Press. 1972. p.79-91.
- PMID 2720141.
- ^ Lyubarev A. E., Kurganov B. I. Supramolecular organisation of Tricarboxylic Acids Cycle's enzymes. Proceedings of the All-Union Symposium "Molecular mechanisms and regulation of energy metabolism". Puschino, Russia, 1986. p. 13. (in Russian) [1].
- ^ Kurganov B. I, Lyubarev A. E. Hypothetical structure of the complex of glycolytic enzymes (glycolytic metabolon), formed on the membrane of erythrocytes. Molek. Biologia. 1988. V.22, No.6, p. 1605–1613. (in Russian)[2]
- ^ Kurganov B.I., Lyubarev A.E. Enzymes and multienzyme complexes as controllable systems. In: Soviet Scientific Reviews. Section D. Physicochemical Biology Reviews. V. 8 (ed. V.P. Skulachev). Glasgow, Harwood Acad. Publ., 1988, p. 111-147 [3]
- PMID 1111588.
- PMID 6692839.
- .
- ^ Robinson, J. B., Jr. & Srere, P. A. (1986) Interactions of sequential metabolic enzymes of the mitochondria: a role in metabolic regulation, pp. 159–171 in Dynamics of Biochemical Systems (ed. Damjanovich, S., Keleti, T. & Trón, L.), Akadémiai Kiadó, Budapest, Hungary
- PMID 28743795.
- ISBN 978-966-613-538-7