Conversion of the allosteric transition of GroEL from concerted to sequential by the single mutation Asp-155→Ala

被引:33
作者
Danziger, O
Rivenzon-Segal, D
Wolf, SG
Horovitz, A [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Struct, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Chem Res Support, IL-76100 Rehovot, Israel
关键词
allostery; chaperonin; protein folding; cooperativity; electron microscopy;
D O I
10.1073/pnas.2333925100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The reaction cycle of the double-ring chaperonin GroEL is driven by ATP binding that takes place with positive cooperativity within each seven-membered ring and negative cooperativity between rings. The positive cooperativity within rings is due to ATP binding-induced conformational changes that are fully concerted. Herein, it is shown that the mutation Asp-155 --> Ala leads to an ATP-induced break in intra-ring and inter-ring symmetry. Electron microscopy analysis of single-ring GroEL particles containing the Asp-155 Ala mutation shows that the break in intra-ring symmetry is due to stabilization of allosteric intermediates such as one in which three subunits have switched their conformation while the other four have not. Our results show that eliminating an intra-subunit interaction between Asp-155 and Arg-395 results in conversion of the allosteric switch of GroEL from concerted to sequential, thus demonstrating that its allosteric behavior arises from coupled tertiary conformational changes.
引用
收藏
页码:13797 / 13802
页数:6
相关论文
共 33 条
[21]  
Saibil HR, 2002, ADV PROTEIN CHEM, V59, P45
[22]   Synchronized domain-opening motion of GroEL is essential for communication between the two rings [J].
Shiseki, K ;
Murai, N ;
Motojima, F ;
Hisabori, T ;
Yoshida, M ;
Taguchi, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :11335-11338
[23]   Chaperonin function: Folding by forced unfolding [J].
Shtilerman, M ;
Lorimer, GH ;
Englander, SW .
SCIENCE, 1999, 284 (5415) :822-825
[24]   AFFINITY OF CHAPERONIN-60 FOR A PROTEIN SUBSTRATE AND ITS MODULATION BY NUCLEOTIDES AND CHAPERONIN-10 [J].
STANIFORTH, RA ;
BURSTON, SG ;
ATKINSON, T ;
CLARKE, AR .
BIOCHEMICAL JOURNAL, 1994, 300 :651-658
[25]   Chaperonin-mediated protein folding [J].
Thirumalai, D ;
Lorimer, GH .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2001, 30 :245-269
[26]   MECHANISM OF GROEL ACTION - PRODUCTIVE RELEASE OF POLYPEPTIDE FROM A SEQUESTERED POSITION UNDER GROES [J].
WEISSMAN, JS ;
HOHL, CM ;
KOVALENKO, O ;
KASHI, Y ;
CHEN, SX ;
BRAIG, K ;
SAIBIL, HR ;
FENTON, WA ;
HORWICH, AL .
CELL, 1995, 83 (04) :577-587
[27]   The crystal structure of the asymmetric GroEL-GroES-(ADP)(7) chaperonin complex [J].
Xu, ZH ;
Horwich, AL ;
Sigler, PB .
NATURE, 1997, 388 (6644) :741-750
[28]   Transient kinetic analysis of adenosine 5′-triphosphate binding-induced conformational changes in the allosteric chaperonin GroEL [J].
Yifrach, O ;
Horovitz, A .
BIOCHEMISTRY, 1998, 37 (20) :7083-7088
[29]   2 LINES OF ALLOSTERIC COMMUNICATION IN THE OLIGOMERIC CHAPERONIN GROEL ARE REVEALED BY THE SINGLE MUTATION ARG196-]ALA [J].
YIFRACH, O ;
HOROVITZ, A .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 243 (03) :397-401
[30]   NESTED COOPERATIVITY IN THE ATPASE ACTIVITY OF THE OLIGOMERIC CHAPERONIN GROEL [J].
YIFRACH, O ;
HOROVITZ, A .
BIOCHEMISTRY, 1995, 34 (16) :5303-5308