Room-Temperature Distance Measurements of Immobilized Spin-Labeled Protein by DEER/PELDOR

被引:78
作者
Meyer, Virginia [1 ]
Swanson, Michael A. [1 ]
Clouston, Laura J. [3 ]
Boratynski, Przemysaw J. [3 ]
Stein, Richard A. [2 ]
Mchaourab, Hassane S. [2 ]
Rajca, Andrzej [3 ]
Eaton, Sandra S. [1 ]
Eaton, Gareth R. [1 ]
机构
[1] Univ Denver, Dept Chem & Biochem, Denver, CO 80208 USA
[2] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[3] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
关键词
ELECTRON-ELECTRON RESONANCE; DIPOLAR ESR SPECTROSCOPY; RELAXATION-TIMES; EPR SPECTROSCOPY; T4; LYSOZYME; NITROXIDES; RADICALS; DISTRIBUTIONS; TREHALOSE; DYNAMICS;
D O I
10.1016/j.bpj.2015.01.015
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Nitroxide spin labels are used for double electron-electron resonance (DEER) measurements of distances between sites in biomolecules. Rotation of gem-dimethyls in commonly used nitroxides causes spin echo dephasing times (T-m) to be too short to perform DEER measurements at temperatures between similar to 80 and 295 K, even in immobilized samples. A spirocyclohexyl spin label has been prepared that has longer T-m between 80 and 295 K in immobilized samples than conventional labels. Two of the spirocyclohexyl labels were attached to sites on T4 lysozyme introduced by site-directed spin labeling. Interspin distances up to similar to 4 nm were measured by DEER at temperatures up to 160 K in water/glycerol glasses. In a glassy trehalose matrix the T-m for the doubly labeled T4 lysozyme was long enough to measure an interspin distance of 3.2 nm at 295 K, which could not be measured for the same protein labeled with the conventional 1-oxyl-2,2,5,5-tetramethyl-3-pyrroline-3-(methyl) methanethio-sulfonate label.
引用
收藏
页码:1213 / 1219
页数:7
相关论文
共 35 条
[1]   Self-Association of the Histidine Kinase CheA as Studied by Pulsed Dipolar ESR Spectroscopy [J].
Bhatnagar, Jaya ;
Sircar, Ria ;
Borbat, Peter P. ;
Freed, Jack H. ;
Crane, Brian R. .
BIOPHYSICAL JOURNAL, 2012, 102 (09) :2192-2201
[2]   Measuring distances by pulsed dipolar ESR spectroscopy: Spin-labeled histidine kinases [J].
Borbat, Peter P. ;
Freed, Jack H. .
TWO-COMPONENT SIGNALING SYSTEMS, PT B, 2007, 423 :52-+
[3]   Improved Sensitivity for Long-Distance Measurements in Biomolecules: Five-Pulse Double Electron-Electron Resonance [J].
Borbat, Peter P. ;
Georgieva, Elka R. ;
Freed, Jack H. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2013, 4 (01) :170-175
[4]   Protein structure determination using long-distance constraints from double-quantum coherence ESR: Study of T4 lysozyme [J].
Borbat, PP ;
Mchaourab, HS ;
Freed, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (19) :5304-5314
[5]   The determination of pair distance distributions by pulsed ESR using Tikhonov regularization [J].
Chiang, YW ;
Borbat, PP ;
Freed, JH .
JOURNAL OF MAGNETIC RESONANCE, 2005, 172 (02) :279-295
[6]   Microscopic mechanism of protein cryopreservation in an aqueous solution with trehalose [J].
Corradini, Dario ;
Strekalova, Elena G. ;
Stanley, H. Eugene ;
Gallo, Paola .
SCIENTIFIC REPORTS, 2013, 3
[7]   The role of vitrification in anhydrobiosis [J].
Crowe, JH ;
Carpenter, JF ;
Crowe, LM .
ANNUAL REVIEW OF PHYSIOLOGY, 1998, 60 :73-103
[8]   Tryptophan interactions with glycerol/water and trehalose/sucrose cryosolvents: infrared and fluorescence spectroscopy and ab initio calculations [J].
Dashnau, JL ;
Zelent, B ;
Vanderkooi, JM .
BIOPHYSICAL CHEMISTRY, 2005, 114 (01) :71-83
[9]   SUPERSLOW ROTATIONS OF NITROXIDE RADICALS STUDIED BY PULSE ELECTRON-PARAMAGNETIC-RES SPECTROSCOPY [J].
DZUBA, SA ;
MARYASOV, AG ;
SALIKHOV, KM ;
TSVETKOV, YD .
JOURNAL OF MAGNETIC RESONANCE, 1984, 58 (01) :95-117
[10]  
Eaton SS, 2000, BIO MAGN RE, V19, P29