Structure of the elongating ribosome:: Arrangement of the two tRNAs before and after translocation

被引:27
作者
Nierhaus, KH
Wadzack, J
Burkhardt, N
Jünemann, R
Meerwinck, W
Willumeit, R
Stuhrmann, HB
机构
[1] Max Planck Inst Mol Genet, AG Ribosomen, D-14195 Berlin, Germany
[2] GKSS Forschungszentrum Geesthacht GmbH, D-21502 Geesthacht, Germany
关键词
protein synthesis; neutron scattering; tRNA binding sites;
D O I
10.1073/pnas.95.3.945
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 ribosome uses tRNAs to translate the genetic information into the amino acid sequence of proteins, The mass ratio of a tRNA to the ribosome is in the order of 1:100; because of this unfavorable value it was not possible until now to determine the location of tRNAs within the ribosome by neutron-scattering techniques, However, the new technique of proton-spin contrast-variation improves the signal-to-noise ratio by more than one order of magnitude, thus enabling the direct determination of protonated tRNAs within a deuterated ribosome for the first time. Here we analyze a pair of ribosomal complexes being either in the pre- or post-translocational states that represent the main states of the elongating ribosome, Both complexes were derived from one preparation, The orientation of both tRNAs within the ribosome and their mutual arrangement are determined by using an electron microscopy model for the Escherichia coli ribosome and the tRNA structure, The mass center of gravity of the (tRNA)(2)mRNA complex moves within the ribosome by 12 +/- 4 Angstrom in the course of translocation as previously reported, The main results of the present analysis are that the mutual arrangement of the two tRNAs does not change on translocation and that the angle between them is, depending on the model used, 110 degrees +/- 10 degrees before and after translocation, The translocational movement of the constant tRNA complex within the ribosome can be described as a displacement toward the head of the 30S subunit combined with a rotational movement by about 18 degrees.
引用
收藏
页码:945 / 950
页数:6
相关论文
共 33 条
[21]  
OLSON HM, 1988, J BIOL CHEM, V263, P15196
[22]   STRUCTURE OF YEAST PHENYLALANINE TRANSFER-RNA AT 3 A RESOLUTION [J].
ROBERTUS, JD ;
LADNER, JE ;
FINCH, JT ;
RHODES, D ;
BROWN, RS ;
CLARK, BFC ;
KLUG, A .
NATURE, 1974, 250 (5467) :546-551
[23]  
SCHILLINGBARTETZKO S, 1992, J BIOL CHEM, V267, P4703
[24]   LOCALIZATION OF THE 3' END OF ESCHERICHIA-COLI 16-S RNA BY ELECTRON-MICROSCOPY OF ANTIBODY-LABELED SUBUNITS [J].
SHATSKY, IN ;
MOCHALOVA, LV ;
KOJOUHAROVA, MS ;
BOGDANOV, AA ;
VASILIEV, VD .
JOURNAL OF MOLECULAR BIOLOGY, 1979, 133 (04) :501-515
[25]   TRANSFER-RNA TRANSFER-RNA INTERACTIONS WITHIN CELLULAR RIBOSOMES [J].
SMITH, D ;
YARUS, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4397-4401
[26]   Arrangement of tRNAs in pre- and posttranslocational ribosomes revealed by electron cryomicroscopy [J].
Stark, H ;
Orlova, EV ;
RinkeAppel, J ;
Junke, N ;
Mueller, F ;
Rodnina, M ;
Wintermeyer, W ;
Brimacombe, R ;
vanHeel, M .
CELL, 1997, 88 (01) :19-28
[27]  
STOFFLER G, 1986, STRUCTURE FUNCTION G, P28
[28]   PROTON AND DEUTERON SPIN TARGETS IN BIOLOGICAL STRUCTURE RESEARCH [J].
STUHRMANN, HB ;
BURKHARDT, N ;
DIETRICH, G ;
JUNEMANN, R ;
MEERWINCK, W ;
SCHMITT, M ;
WADZACK, J ;
WILLUMEIT, R ;
ZHAO, J ;
NIERHAUS, KH .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 1995, 356 (01) :124-132
[29]   PUROMYCIN REACTION + ITS RELATION TO PROTEIN SYNTHESIS [J].
TRAUT, RR ;
MONRO, RE .
JOURNAL OF MOLECULAR BIOLOGY, 1964, 10 (01) :63-+
[30]   Direct localization of the tRNAs within the elongating ribosome by means of neutron scattering (proton-spin contrast-variation) [J].
Wadzack, J ;
Burkhardt, N ;
Junemann, R ;
Diedrich, G ;
Nierhaus, KH ;
Frank, J ;
Penczek, P ;
Meerwinck, W ;
Schmitt, M ;
Willumeit, R ;
Stuhrmann, HB .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 266 (02) :343-356