Literature DB >> 22341208

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

Elka R Georgieva1, Aritro S Roy, Vladimir M Grigoryants, Petr P Borbat, Keith A Earle, Charles P Scholes, Jack H Freed.   

Abstract

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 μs) 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. Copyright Â
© 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22341208      PMCID: PMC3323113          DOI: 10.1016/j.jmr.2012.01.004

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  30 in total

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3.  Effect of the environment on the protein dynamical transition: a neutron scattering study.

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4.  The determination of pair distance distributions by pulsed ESR using Tikhonov regularization.

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8.  Multifrequency electron spin resonance study of the dynamics of spin labeled T4 lysozyme.

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  41 in total

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6.  Genetic Incorporation of the Unnatural Amino Acid p-Acetyl Phenylalanine into Proteins for Site-Directed Spin Labeling.

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7.  Tau binds to lipid membrane surfaces via short amphipathic helices located in its microtubule-binding repeats.

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10.  Room-temperature distance measurements of immobilized spin-labeled protein by DEER/PELDOR.

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