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网格蛋白的稳定性与结构

Stability and structure of clathrin.

作者信息

Edelhoch H, Prasad K, Lippoldt R E, Nandi P K

出版信息

Biochemistry. 1984 May 8;23(10):2314-20. doi: 10.1021/bi00305a035.

Abstract

The effects of urea on the dissociation and structural transitions of clathrin (8 S) have been evaluated by various techniques. The dissociation of the light chains in 3 M urea has been shown by light scattering, ultracentrifugation, and column chromatography. The dissociated components still retain the capacity to form the characteristic polygonal structure of the coat after removal of the urea. At higher concentrations of urea, the secondary and tertiary structures are eliminated, as documented by various spectroscopic techniques, i.e., tryptophan polarization and emission maxima, circular dichroism, and difference spectra. Two distinct transitions are observed by all techniques, one between 3 and 6 M urea and a second one which starts at 7 M but is still incomplete by 9.6 M urea. A concentration-dependent aggregation of clathrin chains occurs in 4 and 5 M urea solutions, as observed by light scattering and sedimentation. The results indicate that there are two large, independent domains in clathrin heavy chains and that each domain may have a single, highly cooperative transition.

摘要

已通过多种技术评估了尿素对网格蛋白(8S)解离和结构转变的影响。通过光散射、超速离心和柱色谱法已证明在3M尿素中轻链会发生解离。去除尿素后,解离的组分仍保留形成衣被特征多边形结构的能力。在较高浓度的尿素中,二级和三级结构会被消除,各种光谱技术,即色氨酸极化和发射最大值、圆二色性和差光谱,都证明了这一点。所有技术均观察到两个明显的转变,一个在3至6M尿素之间,另一个始于7M但在9.6M尿素时仍未完成。通过光散射和沉降观察到,在4M和5M尿素溶液中网格蛋白链会发生浓度依赖性聚集。结果表明,网格蛋白重链中有两个大的独立结构域,并且每个结构域可能有一个单一的、高度协同的转变。

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