A new view of protein synthesis: Mapping the free energy landscape of the ribosome using single-molecule FRET

被引:41
作者
Munro, James B. [1 ]
Vaiana, Andrea [2 ]
Sanbonmatsu, Kevin Y. [2 ]
Blanchard, Scott C. [1 ]
机构
[1] Cornell Univ, Weill Cornell Med Coll, Dept Physiol & Biophys, Ithaca, NY 14853 USA
[2] Los Alamos Natl Lab, Div Theoret, Theoret Biol & Biophys Grp, Los Alamos, NM USA
关键词
single-molecule; FRET; ribosome; translation; tRNA;
D O I
10.1002/bip.20961
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
This article reviews the application of single-molecule fluorescence resonance energy transfer (smFRET) methods to the study of protein synthesis catalyzed by the ribosome. smFRET is a powerful new technique that can be used to investigate dynamic processes within enzymes spanning many orders of magnitude. The application of wide-field smFRET imaging methods to the study of dynamic processes in the ribosome offers a new perspective on the mechanism of protein synthesis. Using this technique, the structural and kinetic parameters Of tRNA motions within wild-type and specifically mutated ribosome complexes have been obtained that provide valuable new insights into the mechanism and regulation of translation elongation. The results of these studies are discussed in the context of current knowledge of the ribosome mechanism from both structural and biophysical perspectives. (c) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:565 / 577
页数:13
相关论文
共 122 条
[1]   Effect of buffer conditions on the position of tRNA on the 70 S ribosome as visualized by cryoelectron microscopy [J].
Agrawal, RK ;
Penczek, P ;
Grassucci, RA ;
Burkhardt, N ;
Nierhaus, KH ;
Frank, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8723-8729
[2]   Direct visualization of A-, P-, and E-site transfer RNAs in the Escherichia coli ribosome [J].
Agrawal, RK ;
Penczek, P ;
Grassucci, RA ;
Li, YH ;
Leith, A ;
Nierhaus, KH ;
Frank, J .
SCIENCE, 1996, 271 (5251) :1000-1002
[3]   EF-G-dependent GTP hydrolysis induces translocation accompanied by large conformational changes in the 70S ribosome [J].
Agrawal, RK ;
Heagle, AB ;
Penczek, P ;
Grassucci, RA ;
Frank, J .
NATURE STRUCTURAL BIOLOGY, 1999, 6 (07) :643-647
[4]  
AGRAWAL RK, 1998, J MOL BIOL CELL, V9, P405
[5]  
AITKEN CE, 2007, BIOPHYS J
[6]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[7]   FLUORESCENCE SPECTROSCOPY AND SPECTRAL DIFFUSION OF SINGLE IMPURITY MOLECULES IN A CRYSTAL [J].
AMBROSE, WP ;
MOERNER, WE .
NATURE, 1991, 349 (6306) :225-227
[8]   Dynamic polymorphism of Ras observed by single molecule FRET is the basis for molecular recognition [J].
Arai, Y ;
Iwane, AH ;
Wazawa, T ;
Yokota, H ;
Ishii, Y ;
Kataoka, T ;
Yanagida, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 343 (03) :809-815
[9]  
BERGEMANN K, 1983, J BIOL CHEM, V258, P5105
[10]   The ribosomal peptidyl transferase [J].
Beringer, Malte ;
Rodnina, Marina V. .
MOLECULAR CELL, 2007, 26 (03) :311-321