Interaction of 4,4'-dithiodipyridine with Cys(458) triggers disassembly of GroEL

J Biol Chem. 1999 Jul 23;274(30):20756-8. doi: 10.1074/jbc.274.30.20756.

Abstract

Chaperonin GroEL, consisting of two seven-subunit rings stacked back-to-back, is disassembled by interaction of 4, 4'-dithiodipyridine (DTP) with Cys(458) located close to the intersubunit contacts within and between the rings. The thiol group of Cys(458) is inaccessible to the probe being buried into the pocket locked by segment Asn(475)-Asn(487). Flexibility of this segment is proposed to induce the "open" state of the pocket and accommodate the bulky probe inside so that the consequential irreversible shifts in the pocket constituents disassemble GroEL. This scheme is supported by the finding that DTP-induced disassembly of GroEL is facilitated by ATP, which specifically stimulates a local shift of the segment Asn(475)-Asn(487) into solution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chaperonin 60 / chemistry*
  • Chaperonin 60 / metabolism
  • Cysteine / chemistry
  • Cysteine / metabolism
  • Disulfides / metabolism*
  • Protein Conformation*
  • Pyridines / metabolism*
  • Sulfhydryl Reagents / metabolism

Substances

  • Chaperonin 60
  • Disulfides
  • Pyridines
  • Sulfhydryl Reagents
  • 4,4'-dipyridyl disulfide
  • Cysteine