Gain-of-function mutations reveal expanded intermediate states and a sequential action of two gates in MscL

被引:66
作者
Anishkin, A [1 ]
Chiang, CS [1 ]
Sukharev, S [1 ]
机构
[1] Univ Maryland, Dept Biol, College Pk, MD 20742 USA
关键词
mechanosensitive channel; tension; thermodynamics; subconducting states; hydration;
D O I
10.1085/jgp.200409118
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The tension-driven gating transition in the large mechanosensitive channel MscL proceeds through detectable states of intermediate conductance. Gain-of-function (GOF) mutants with polar or charged substitutions in the main hydrophobic gate display altered patterns of subconducting states, providing valuable information about gating intermediates. Here we present thermodynamic analysis of several GOF mutants to clarify the nature and position of low-conducting conformations in the transition pathway. Unlike wild-type (WT) MscL, which predominantly occupies the closed and fully open states with very brief substates, the mild V23T GOF mutant frequently visits a multitude of short-lived subconducting states. Severe mutants V23D and G22N open in sequence: closed (C) --> low-conducting substate (S) --> open (O), with the first subtransition occurring at lower tensions. Analyses of equilibrium state occupancies as functions Of Membrane tension show that the C --> S subtransition in WT MscL is associated with only a minor conductance increment, but the largest in-plane expansion and free energy change. The GOF substitutions strongly affect the first subtransition by reducing area (AA) and energy (DeltaE) changes between C and S states commensurably with the severity of mutation. GOF mutants also exhibited a considerably larger DeltaE associated with the second (S --> O) subtransition, but a DeltaA similar to WE The area changes indicate that closed conformations of GOF mutants are physically preexpanded. The tension dependencies of rate constants for channel closure (huff) predict different positions of rate-limiting barriers on the energy area profiles for WT and GOF MscL. The data support the two-gate mechanism in which the first subtransition (C --> S) can be viewed as opening of the central (M1) gate, resulting in an expanded water-filled "leaky" conformation. Strong facilitation of this step by polar GOF substitutions suggests that separation of M1 helices associated with hydration of the pore in WT MscL is the major energetic barrier for opening. Mutants with a stabilized S1 gate demonstrate impeded transitions from low-conducting substates to the fully open state, whereas extensions of S1-M1 linkers result in a much higher probability of reverse O --> S transitions. These data strongly suggest that the bulk of conductance gain in the second subtransition (S --> O) occurs through the opening of the NH2-terminal (SI) gate and the linkers are coupling elements between the M1 and S1 gates.
引用
收藏
页码:155 / 170
页数:16
相关论文
共 39 条
  • [1] Contributions of the different extramembranous domains of the mechanosensitive ion channel MscL to its response to membrane tension
    Ajouz, B
    Berrier, C
    Besnard, M
    Martinac, B
    Ghazi, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (02) : 1015 - 1022
  • [2] Water dynamics and dewetting transitions in the small mechanosensitive channel MscS
    Anishkin, A
    Sukharev, S
    [J]. BIOPHYSICAL JOURNAL, 2004, 86 (05) : 2883 - 2895
  • [3] On the conformation of the COOH-terminal domain of the large mechanosensitive channel MscL
    Anishkin, A
    Gendel, V
    Sharifi, NA
    Chiang, CS
    Shirinian, L
    Guy, HR
    Sukharev, S
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2003, 121 (03) : 227 - 244
  • [4] BARTLETT JL, 2004, IN PRESS P NATL ACAD
  • [5] Crystal structure of Escherichia coli MscS, a voltage-modulated and mechanosensitive channel
    Bass, RB
    Strop, P
    Barclay, M
    Rees, DC
    [J]. SCIENCE, 2002, 298 (5598) : 1582 - 1587
  • [6] Channel gate! Tension, leak and disclosure
    Batiza, AF
    Rayment, I
    Kung, C
    [J]. STRUCTURE, 1999, 7 (05) : R99 - R103
  • [7] Ion channel gating: insights via molecular simulations
    Beckstein, O
    Biggin, PC
    Bond, P
    Bright, JN
    Domene, C
    Grottesi, A
    Holyoake, J
    Sansom, MSP
    [J]. FEBS LETTERS, 2003, 555 (01) : 85 - 90
  • [8] A large iris-like expansion of a mechanosensitive channel protein induced by membrane tension
    Betanzos, M
    Chiang, CS
    Guy, HR
    Sukharev, S
    [J]. NATURE STRUCTURAL BIOLOGY, 2002, 9 (09) : 704 - 710
  • [9] Molecular mechanisms of mechanosensation: Big lessons from small cells
    Blount, P
    [J]. NEURON, 2003, 37 (05) : 731 - 734
  • [10] Single residue substitutions that change the gating properties of a mechanosensitive channel in Escherichia coli
    Blount, P
    Sukharev, SI
    Schroeder, MJ
    Nagle, SK
    Kung, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) : 11652 - 11657