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利用¹³C或¹⁵N弛豫数据简单准确地测定蛋白质中的全局tau(R)

Simple and accurate determination of global tau(R) in proteins using (13)C or (15)N relaxation data.

作者信息

Mispelter J, Izadi-Pruneyre N, Quiniou E, Adjadj E

机构信息

U350 INSERM, Institut Curie, Laboratoires R. Latarjet, Orsay, F-91405, France.

出版信息

J Magn Reson. 2000 Mar;143(1):229-32. doi: 10.1006/jmre.1999.2006.

Abstract

In the study of protein dynamics by (13)C or (15)N relaxation measurements different models from the Lipari-Szabo formalism are used in order to determine the motion parameters. The global rotational correlation time tau(R) of the molecule must be estimated prior to the analysis. In this Communication, the authors propose a new approach in determining an accurate value for tau(R) in order to realize the best fit of R(2) for the whole sequence of the protein, regardless of the different type of motions atoms may experience. The method first determines the highly structured regions of the sequence. For each corresponding site, the Lipari-Szabo parameters are calculated for R(1) and NOE, using an arbitrary value for tau(R). The chi(2) for R(2), summed over the selected sites, shows a clear minimum, as a function of tau(R). This minimum is used to better estimate a proper value for tau(R).

摘要

在通过¹³C或¹⁵N弛豫测量研究蛋白质动力学时,为了确定运动参数,使用了来自Lipari-Szabo形式主义的不同模型。在分析之前必须估计分子的全局旋转相关时间τ(R)。在本通讯中,作者提出了一种确定τ(R)准确值的新方法,以便实现蛋白质整个序列的R₂的最佳拟合,而不管原子可能经历的不同运动类型如何。该方法首先确定序列的高度结构化区域。对于每个相应位点,使用τ(R)的任意值计算R₁和NOE的Lipari-Szabo参数。针对所选位点求和的R₂的χ²显示出作为τ(R)函数的明显最小值。该最小值用于更好地估计τ(R)的合适值。

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