Literature DB >> 9571111

Improved Estimation of Protein Rotational Correlation Times from 15N Relaxation Measurements

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Abstract

In the study of protein backbone dynamics by 15N relaxation measurements, an initial estimation of the isotropic global correlation time, taum, is usually obtained from the average T1/T2 ratio of nuclear spins that do not exhibit slow internal motion and with T2 values not significantly shortened by chemical or conformational exchange processes. Different methods have been used for identification of the rates of internal motion. However, the number of nuclear spins included in the taum estimation is often larger than the number that ultimately can be fitted to a single-order parameter, S2, implying that some nuclear spins involved in the initial taum estimation actually have an effective internal correlation time, taue, not as fast as assumed. As a consequence, taum is underestimated, since internal motion reduces the T1/T2 ratio. This situation becomes more obvious if the molecule has a large taum value because the reduction in T1/T2 ratio arising from internal motion is more significant than for molecules with smaller taum and the same degree of internal motion. This Communication describes a more reliable method for identifying nuclear spins which should be excluded from the taum estimation because of insufficiently rapid internal motion. This results in an improved taum value, giving a much better agreement between the number of nuclear spins fitted successfully to a single-order parameter, S2, and those used in the taum estimation. Copyright 1998 Academic Press.

Entities:  

Year:  1998        PMID: 9571111     DOI: 10.1006/jmre.1998.1382

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


  6 in total

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2.  Backbone dynamics measurements on leukemia inhibitory factor, a rigid four-helical bundle cytokine.

Authors:  S Yao; D K Smith; M G Hinds; J G Zhang; N A Nicola; R S Norton
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3.  Peptide inhibitors of the malaria surface protein, apical membrane antigen 1: identification of key binding residues.

Authors:  Erinna F Lee; Shenggen Yao; Jennifer K Sabo; W Douglas Fairlie; Rachel A Stevenson; Karen S Harris; Robin F Anders; Michael Foley; Raymond S Norton
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4.  Anisotropic rotational diffusion in model-free analysis for a ternary DHFR complex.

Authors:  M J Osborne; P E Wright
Journal:  J Biomol NMR       Date:  2001-03       Impact factor: 2.835

5.  Mechanistic basis of substrate-O2 coupling within a chitin-active lytic polysaccharide monooxygenase: An integrated NMR/EPR study.

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Review 6.  NMR measurement of biomolecular translational and rotational motion for evaluating changes of protein oligomeric state in solution.

Authors:  Shenggen Yao; David W Keizer; Jeffrey J Babon; Frances Separovic
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  6 in total

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