Pushing, pulling and trapping - Modes of motor protein supported protein translocation

被引:51
作者
Tomkiewicz, Danuta
Nouwen, Nico
Driessen, Arnold J. M.
机构
[1] Univ Groningen, Dept Microbiol, Groningen Biomol Sci & Biotechnol Inst, NL-9751 NN Haren, Netherlands
[2] Univ Groningen, Zernike Inst Adv Mat, NL-9751 NN Haren, Netherlands
来源
FEBS LETTERS | 2007年 / 581卷 / 15期
关键词
translocation; molecular motor; secretory protein; SecA; BiP; Hsp70;
D O I
10.1016/j.febslet.2007.04.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein translocation across the cellular membranes is an ubiquitous and crucial activity of cells. This process is mediated by translocases that consist of a protein conducting channel and an associated motor protein. Motor proteins interact with protein substrates and utilize the free energy of ATP binding and hydrolysis for protein unfolding, translocation and unbinding. Since motor proteins are found either at the cis- or trans-side of the membrane, different mechanisms for translocation have been proposed. In the Power stroke model, cis-acting motors are thought to push, while trans-motors pull on the substrate protein during translocation. In the Brownian ratchet model, translocation occurs by diffusion of the unfolded polypeptide through the translocation pore while directionality is achieved by trapping and refolding. Recent insights in the structure and function of the molecular motors suggest that different mechanisms can be employed simultaneously. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2820 / 2828
页数:9
相关论文
共 87 条
[1]   The molecular mechanisms underlying BiP-mediated gating of the Sec61 translocon of the endoplasmic reticulum [J].
Alder, NN ;
Shen, Y ;
Brodsky, JL ;
Hendershot, LM ;
Johnson, AE .
JOURNAL OF CELL BIOLOGY, 2005, 168 (03) :389-399
[2]   Energetics of protein transport across biological membranes:: A study of the thylakoid ΔpH-dependent/cpTat pathway [J].
Alder, NN ;
Theg, SM .
CELL, 2003, 112 (02) :231-242
[3]   TRANSLOCATION CAN DRIVE THE UNFOLDING OF A PREPROTEIN DOMAIN [J].
ARKOWITZ, RA ;
JOLY, JC ;
WICKNER, W .
EMBO JOURNAL, 1993, 12 (01) :243-253
[4]   Three-dimensional structure of the bacterial protein-translocation complex SecYEG [J].
Breyton, C ;
Haase, W ;
Rapoport, TA ;
Kühlbrandt, W ;
Collinson, I .
NATURE, 2002, 418 (6898) :662-665
[5]   ISOLATION OF A MOUSE CDNA-ENCODING MTJ1, A NEW MURINE MEMBER OF THE DNAJ FAMILY OF PROTEINS [J].
BRIGHTMAN, SE ;
BLATCH, GL ;
ZETTER, BR .
GENE, 1995, 153 (02) :249-254
[6]   BIP AND SEC63P ARE REQUIRED FOR BOTH CO- AND POSTTRANSLATIONAL PROTEIN TRANSLOCATION INTO THE YEAST ENDOPLASMIC-RETICULUM [J].
BRODSKY, JL ;
GOECKELER, J ;
SCHEKMAN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (21) :9643-9646
[7]   Subunits of the translocon interact with components of the oligosaccharyl transferase complex [J].
Chavan, M ;
Yan, AX ;
Lennarz, WJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (24) :22917-22924
[8]   Covalently dimerized SecA is functional in protein translocation [J].
de Keyzer, J ;
van der Sluis, EO ;
Spelbrink, REJ ;
Nijstad, N ;
de Kruijff, B ;
Nouwen, N ;
van der Does, C ;
Driessen, AJM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (42) :35255-35260
[9]   The bacterial translocase: a dynamic protein channel complex [J].
de Keyzer, J ;
van der Does, C ;
Driessen, AJM .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (10) :2034-2052
[10]   Hsp70 chaperones accelerate protein translocation and the unfolding of stable protein aggregates by entropic pulling [J].
De los Rios, P ;
Ben-Zvi, A ;
Slutsky, O ;
Azem, A ;
Goloubinoff, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (16) :6166-6171