A thorough dynamic interpretation of residual dipolar couplings in ubiquitin

被引:68
作者
Lakomek, NA
Carlomagno, T
Becker, S
Griesinger, C
Meiler, J
机构
[1] Max Planck Inst Biophys Chem, NMR Based Struct Biol, D-37077 Gottingen, Germany
[2] Vanderbilt Univ, Dept Chem, Ctr Struct Biol, Nashville, TN 37232 USA
关键词
dynamical averaging; model free approach; nuclear magnetic resonance (NMR); residual dipolar couplings (rdcs); ubiquitin;
D O I
10.1007/s10858-005-5686-0
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
The presence of slow motions with large amplitudes, as detected by measurements based on residual dipolar couplings [Peti, W., Meiler, J., Brueschweiler, R. and Griesinger, C. (2002) J. Am. Chem. Soc., 124, 5822-5833], has stirred up much discussion in recent years. Based on ubiquitin NH residual dipolar couplings (rdcs) measured in 31 different alignment conditions, a model-free analysis of structure and dynamics [Meiler, J., Peti, W., Prompers, J., Griesinger, C. and Brueschweiler, R. (2001) J. Am. Chem. Soc., 123, 6098-6107] is presented. Starting from this broad experimental basis, rdc-based order parameters with so far unattained accuracy were determined. These rdc-based order parameters underpin the presence of new modes of motion slower than the inverse overall tumbling correlation time. Amplitudes and anisotropies of the motion were derived. The effect of structural noise on the results was proven to be negligible.
引用
收藏
页码:101 / 115
页数:15
相关论文
共 60 条
[1]   Monitoring macromolecular motions on microsecond to millisecond time scales by R(1)rho-R(1) constant relaxation time NMR spectroscopy [J].
Akke, M ;
Palmer, AG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (04) :911-912
[2]   Characterization of surfactant liquid crystal phases suitable for molecular alignment and measurement of dipolar couplings [J].
Barrientos, LG ;
Dolan, C ;
Gronenborn, AM .
JOURNAL OF BIOMOLECULAR NMR, 2000, 16 (04) :329-337
[3]   Surface hydrophobic residues of multiubiquitin chains essential for proteolytic targeting [J].
Beal, R ;
Deveraux, Q ;
Xia, G ;
Rechsteiner, M ;
Pickart, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :861-866
[4]   Anisotropic small amplitude peptide plane dynamics in proteins from residual dipolar couplings [J].
Bernadó, P ;
Blackledge, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (15) :4907-4920
[5]   Local dynamic amplitudes on the protein backbone from dipolar couplings:: Toward the elucidation of slower motions in biomolecules [J].
Bernadó, P ;
Blackledge, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (25) :7760-7761
[6]   Release of long-range tertiary interactions potentiates aggregation of natively unstructured α-synuclein [J].
Bertoncini, CW ;
Jung, YS ;
Fernandez, CO ;
Hoyer, W ;
Griesinger, C ;
Jovin, TM ;
Zweckstetter, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (05) :1430-1435
[7]   Locally anisotropic internal polypeptide backbone dynamics by NMR relaxation [J].
Bremi, T ;
Bruschweiler, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (28) :6672-6673
[8]   A protocol for the interpretation of side-chain dynamics based on NMR relaxation: Application to phenylalanines in antamanide [J].
Bremi, T ;
Bruschweiler, R ;
Ernst, RR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (18) :4272-4284
[9]   De Novo determination of bond orientations and order parameters from residual dipolar couplings with high accuracy [J].
Briggman, KB ;
Tolman, JR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (34) :10164-10165
[10]   Backbone dynamics and structural characterization of the partially folded A state of ubiquitin by H-1, C-13, and N-15 nuclear magnetic resonance spectroscopy [J].
Brutscher, B ;
Bruschweiler, R ;
Ernst, RR .
BIOCHEMISTRY, 1997, 36 (42) :13043-13053