Effect of freezing conditions on distances and their distributions derived from Double Electron Electron Resonance (DEER): A study of doubly-spin-labeled T4 lysozyme

被引:85
作者
Georgieva, Elka R. [1 ,2 ]
Roy, Aritro S. [1 ,2 ]
Grigoryants, Vladimir M. [3 ]
Borbat, Petr P. [1 ,2 ]
Earle, Keith A. [1 ,2 ,4 ]
Scholes, Charles P. [3 ]
Freed, Jack H. [1 ,2 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
[2] Cornell Univ, ACERT, Ithaca, NY 14853 USA
[3] SUNY Albany, Dept Chem, Albany, NY 12222 USA
[4] SUNY Albany, Dept Phys, Albany, NY 12222 USA
关键词
Double Electron Electron Resonance (DEER); Pulse dipolar spectroscopy (PDS); T4; lysozyme; Bi-label distance; Bi-label distance distribution; Freezing perturbation; Rapid freeze quench; EXTENDED-HELIX; ESR; BIOMACROMOLECULES; LIQUID;
D O I
10.1016/j.jmr.2012.01.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pulsed dipolar ESR spectroscopy, DEER and DQC, require frozen samples. An important issue in the biological application of this technique is how the freezing rate and concentration of cryoprotectant could possibly affect the conformation of biomacromolecule and/or spin-label. We studied in detail the effect of these experimental variables on the distance distributions obtained by DEER from a series of doubly spin-labeled T4 lysozyme mutants. We found that the rate of sample freezing affects mainly the ensemble of spin-label rotamers, but the distance maxima remain essentially unchanged. This suggests that proteins frozen in a regular manner in liquid nitrogen faithfully maintain the distance-dependent structural properties in solution. We compared the results from rapidly freeze-quenched (<= 100 mu s) samples to those from commonly shock-frozen (slow freeze, 1 s or longer) samples. For all the mutants studied we obtained inter-spin distance distributions, which were broader for rapidly frozen samples than for slowly frozen ones. We infer that rapid freezing trapped a larger ensemble of spin label rotamers; whereas, on the time-scale of slower freezing the protein and spin-label achieve a population showing fewer low-energy conformers. We used glycerol as a cryoprotectant in concentrations of 10% and 30% by weight. With 10% glycerol and slow freezing, we observed an increased slope of background signals, which in DEER is related to increased local spin concentration, in this case due to insufficient solvent vitrification, and therefore protein aggregation. This effect was considerably suppressed in slowly frozen samples containing 30% glycerol and rapidly frozen samples containing 10% glycerol. The assignment of bimodal distributions to tether rotamers as opposed to protein conformations is aided by comparing results using MTSL and 4-Bromo MTSL spin-labels. The latter usually produce narrower distance distributions. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 77
页数:9
相关论文
共 37 条
  • [1] Estimation of inter-residue distances in spin labeled proteins at physiological temperatures: Experimental strategies and practical limitations
    Altenbach, C
    Oh, KJ
    Trabanino, RJ
    Hideg, K
    Hubbell, WL
    [J]. BIOCHEMISTRY, 2001, 40 (51) : 15471 - 15482
  • [2] Lessons from the lysozyme of phage T4
    Baase, Walter A.
    Liu, Lijun
    Tronrud, Dale E.
    Matthews, Brian W.
    [J]. PROTEIN SCIENCE, 2010, 19 (04) : 631 - 641
  • [3] THE RELATIVE MERITS OF VARIOUS COOLING METHODS
    BALD, WB
    [J]. JOURNAL OF MICROSCOPY, 1985, 140 (OCT) : 17 - 40
  • [4] Rigid body refinement of protein complexes with long-range distance restraints from pulsed dipolar ESR
    Bhatnagar, Jaya
    Freed, Jack H.
    Crane, Brian R.
    [J]. TWO-COMPONENT SIGNALING SYSTEMS, PT B, 2007, 423 : 117 - +
  • [5] Structure of the Ternary Complex Formed by a Chemotaxis Receptor Signaling Domain, the CheA Histidine Kinase, and the Coupling Protein CheW As Determined by Pulsed Dipolar ESR Spectroscopy
    Bhatnagar, Jaya
    Borbat, Peter P.
    Pollard, Abiola M.
    Bilwes, Alexandrine M.
    Freed, Jack H.
    Crane, Brian R.
    [J]. BIOCHEMISTRY, 2010, 49 (18) : 3824 - 3841
  • [6] Measuring distances by pulsed dipolar ESR spectroscopy: Spin-labeled histidine kinases
    Borbat, Peter P.
    Freed, Jack H.
    [J]. TWO-COMPONENT SIGNALING SYSTEMS, PT B, 2007, 423 : 52 - +
  • [7] Multifrequency two-dimensional Fourier transform ESR: An X/Ku-band spectrometer
    Borbat, PP
    Crepeau, RH
    Freed, JH
    [J]. JOURNAL OF MAGNETIC RESONANCE, 1997, 127 (02) : 155 - 167
  • [8] Protein structure determination using long-distance constraints from double-quantum coherence ESR: Study of T4 lysozyme
    Borbat, PP
    Mchaourab, HS
    Freed, JH
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (19) : 5304 - 5314
  • [9] Borbat PP., 2007, EPR Newsletter, V17, P21
  • [10] Solution structure of a minor and transiently formed state of a T4 lysozyme mutant
    Bouvignies, Guillaume
    Vallurupalli, Pramodh
    Hansen, D. Flemming
    Correia, Bruno E.
    Lange, Oliver
    Bah, Alaji
    Vernon, Robert M.
    Dahlquist, Frederick W.
    Baker, David
    Kay, Lewis E.
    [J]. NATURE, 2011, 477 (7362) : 111 - U134