Measurement of internal movements within the 30 S ribosomal subunit using Forster resonance energy transfer

被引:52
作者
Hickerson, R
Majumdar, ZK
Baucom, A
Clegg, RM
Noller, HF [1 ]
机构
[1] Univ Calif Santa Cruz, Ctr Mol Biol, RNA, Santa Cruz, CA 95064 USA
[2] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Sinsheimer Labs, Santa Cruz, CA 95064 USA
[3] Univ Illinois, Dept Phys, Fluorescence Dynam Lab, Urbana, IL 61801 USA
关键词
FRET; subunit association; rRNA; ribosomal proteins;
D O I
10.1016/j.jmb.2005.09.010
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
We have used Forster resonance energy transfer (FRET) to study specific conformational changes in the Escherichia coli 30 S ribosomal subunit that occur upon association with the 50 S subunit. By measuring energy transfer between 13 different pairs of fluorescent probes attached to specific positions on 30 S subunit proteins, we have monitored changes in distance between different locations within the 30 S subunit in its free and 50 S-bound states. The measured distance changes provide restraints for modeling the movement that occurs within the 30 S subunit upon formation of the 70 S ribosome in solution. Treating the head, body, and platform domains of the 30 S subunit as simple rigid bodies, the lowest-energy solution converges on a model that satisfies each of the individual FRET restraints. In this model, the 30 S subunit head tilts towards the 50 S subunit, similar to the movement found in comparing 30 S subunits and 70 S ribosomes from X-ray and cryo-electron microscope structures, and the platform is predicted to undergo a clock-wise rotation upon association. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:459 / 472
页数:14
相关论文
共 52 条
[1]   The complete atomic structure of the large ribosomal subunit at 2.4 Å resolution [J].
Ban, N ;
Nissen, P ;
Hansen, J ;
Moore, PB ;
Steitz, TA .
SCIENCE, 2000, 289 (5481) :905-920
[2]   tRNA selection and kinetic proofreading in translation [J].
Blanchard, SC ;
Gonzalez, RL ;
Kim, HD ;
Chu, S ;
Puglisi, JD .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (10) :1008-1014
[3]   tRNA dynamics on the ribosome during translation [J].
Blanchard, SC ;
Kim, HD ;
Gonzalez, RL ;
Puglisi, JD ;
Chu, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :12893-12898
[4]  
Brunger AT, 1998, ACTA CRYSTALLOGR D, V54, P905, DOI 10.1107/s0907444998003254
[5]  
CANTOR CR, 1971, PROCEDURES NUCLEIC A, V2, P31
[6]  
Clegg R.M., 1996, FLUORESCENCE IMAGING, V137, P179
[7]  
CLEGG RM, 1992, METHOD ENZYMOL, V211, P353
[8]   FLUORESCENCE RESONANCE ENERGY-TRANSFER ANALYSIS OF THE STRUCTURE OF THE 4-WAY DNA JUNCTION [J].
CLEGG, RM ;
MURCHIE, AIH ;
ZECHEL, A ;
CARLBERG, C ;
DIEKMANN, S ;
LILLEY, DMJ .
BIOCHEMISTRY, 1992, 31 (20) :4846-4856
[9]   Efficient reconstitution of functional Escherichia coli 30S ribosomal subunits from a complete set of recombinant small subunit ribosomal proteins [J].
Culver, GM ;
Noller, HF .
RNA, 1999, 5 (06) :832-843
[10]  
Culver GM, 2000, METHOD ENZYMOL, V318, P446