Metal Preferences and Metallation

The metal binding preferences of most metalloproteins do not match their metal requirements. Thus, metallation of an estimated 30% of metalloenzymes is aided by metal delivery systems, with ∼25% acquiring preassembled metal cofactors. The remaining ∼70% are presumed to compete for metals from buffer...

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Veröffentlicht in:The Journal of biological chemistry 2014-10, Vol.289 (41), p.28095-28103
Hauptverfasser: Foster, Andrew W., Osman, Deenah, Robinson, Nigel J.
Format: Artikel
Sprache:eng
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Zusammenfassung:The metal binding preferences of most metalloproteins do not match their metal requirements. Thus, metallation of an estimated 30% of metalloenzymes is aided by metal delivery systems, with ∼25% acquiring preassembled metal cofactors. The remaining ∼70% are presumed to compete for metals from buffered metal pools. Metallation is further aided by maintaining the relative concentrations of these pools as an inverse function of the stabilities of the respective metal complexes. For example, magnesium enzymes always prefer to bind zinc, and these metals dominate the metalloenzymes without metal delivery systems. Therefore, the buffered concentration of zinc is held at least a million-fold below magnesium inside most cells.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.R114.588145