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通过高压1H NMR光谱法测定Arc阻遏蛋白单体的熔球构象。

Molten-globule conformation of Arc repressor monomers determined by high-pressure 1H NMR spectroscopy.

作者信息

Peng X, Jonas J, Silva J L

机构信息

Department of Chemistry, School of Chemical Sciences, University of Illinois, Urbana 61801.

出版信息

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1776-80. doi: 10.1073/pnas.90.5.1776.

Abstract

The conformation of the pressure-dissociated monomer of Arc repressor was characterized by 1H NMR spectroscopy. The NMR spectra of the monomer under pressure (up to 5.0 kbar; 1 bar = 100 kPa) are typical of a molten globule and they are considerably different from those of the native dimer and thermally denatured monomer. The two-dimensional nuclear Overhauser effect spectra suggest that the pressure-induced molten globule retains some secondary structure. The presence of nuclear Overhauser effects in the beta-sheet region in the dissociated state suggests that the intermonomer beta-sheet (residues 8-14) in the native dimer is replaced by an intramonomer beta-sheet. Changes in one-dimensional and two-dimensional NMR spectra prior to pressure dissociation were found and suggest the existence of a "predissociated" state.

摘要

通过核磁共振氢谱(1H NMR)对Arc阻遏蛋白压力解离单体的构象进行了表征。压力下(高达5.0千巴;1巴 = 100千帕)单体的核磁共振谱是典型的熔融球状,与天然二聚体和热变性单体的谱有很大不同。二维核Overhauser效应谱表明,压力诱导的熔融球状保留了一些二级结构。解离状态下β折叠区域存在核Overhauser效应,表明天然二聚体中的单体间β折叠(残基8 - 14)被单体内部的β折叠所取代。发现在压力解离之前一维和二维核磁共振谱发生了变化,这表明存在“预解离”状态。

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