Measuring residual dipolar couplings at high hydrostatic pressure: robustness of alignment media to high pressure

被引:7
作者
Sibille, Nathalie [1 ,2 ,3 ,4 ]
Dellarole, Mariano [1 ,2 ,3 ,4 ]
Royer, Catherine [1 ,2 ,3 ,4 ]
Roumestand, Christian [1 ,2 ,3 ,4 ]
机构
[1] CNRS, UMR 5048, CBS, F-34090 Montpellier, France
[2] INSERM, U1054, F-34090 Montpellier, France
[3] Univ Montpellier I, F-34090 Montpellier, France
[4] Univ Montpellier 2, F-34090 Montpellier, France
关键词
High hydrostatic pressure; NMR spectroscopy; Residual dipolar couplings; Alignment media; Folding/unfolding under pressure; LIQUID-CRYSTALLINE MEDIUM; BIOMOLECULAR STRUCTURE; PROTEIN DENATURATION; HYDROGEN-EXCHANGE; ENERGY LANDSCAPE; NMR EXPERIMENTS; MACROMOLECULES; TEMPERATURES; STABILITY; UBIQUITIN;
D O I
10.1007/s10858-013-9798-7
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
Among other perturbations, high hydrostatic pressure has proven to be a mild yet efficient way to unfold proteins. Combining pressure perturbation with NMR spectroscopy allows for a residue-per-residue description of folding reactions. Accessing the full power of NMR spectroscopy under pressure involves the investigation of conformational sampling using orientational restraints such as residual dipolar couplings (RDCs) under conditions of partial alignment. The aim of this study was to identify and characterize stable and pressure resistant alignment media for measurement of RDCs at high pressure. Four alignment media were tested. A C12E5/n-hexanol alcohol mixture remains stable from 1 to 2,500 bar, whereas Pf1 phage and DNA nanotubes undergo a reversible transition between 300 and 900 bar. Phospholipid bicelles are stable only until 300 bar at ambient temperature. Hence, RDCs can be measured at high pressure, and their interpretation will provide atomic details of the structural and dynamic perturbations on unfolded or partially folded states of proteins under pressure.
引用
收藏
页码:9 / 16
页数:8
相关论文
共 44 条
[1]   Weak alignment NMR: a hawk-eyed view of biomolecular structure [J].
Bax, A ;
Grishaev, A .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2005, 15 (05) :563-570
[2]   Recovery of intact DNA nanostructures after agarose gel-based separation [J].
Bellot, Gaetan ;
McClintock, Mark A. ;
Lin, Chenxiang ;
Shih, William M. .
NATURE METHODS, 2011, 8 (03) :192-194
[3]   Recent progress in the study of biomolecular structure and dynamics in solution from residual dipolar couplings [J].
Blackledge, M .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2005, 46 (01) :23-61
[4]   The dynamic energy landscape of dihydrofolate reductase catalysis [J].
Boehr, David D. ;
McElheny, Dan ;
Dyson, H. Jane ;
Wright, Peter E. .
SCIENCE, 2006, 313 (5793) :1638-1642
[5]   Identification of slow correlated motions in proteins using residual dipolar and hydrogen-bond scalar couplings [J].
Bouvignies, G ;
Bernadó, P ;
Meier, S ;
Cho, K ;
Grzesiek, S ;
Brüschweiler, R ;
Blackledge, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :13885-13890
[6]   THERMODYNAMICS OF PROTEIN DENATURATION - EFFECT OF PRESSURE ON DENATURATION OF RIBONUCLEASE-A [J].
BRANDTS, JF ;
OLIVEIRA, RJ ;
WESTORT, C .
BIOCHEMISTRY, 1970, 9 (04) :1038-&
[7]   Pressure-stability of phospholipid bicelles Measurement of residual dipolar couplings under extreme conditions [J].
Brunner, E ;
Arnold, MR ;
Kremer, W ;
Kalbitzer, HR .
JOURNAL OF BIOMOLECULAR NMR, 2001, 21 (02) :173-176
[8]   A doublet-separated sensitivity-enhanced HSQC for the determination of scalar and dipolar one-bond J-couplings [J].
Cordier, F ;
Dingley, AJ ;
Grzesiek, S .
JOURNAL OF BIOMOLECULAR NMR, 1999, 13 (02) :175-180
[9]  
DAquino JA, 1996, PROTEINS, V25, P143, DOI 10.1002/(SICI)1097-0134(199606)25:2<143::AID-PROT1>3.0.CO
[10]  
2-J