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网格蛋白篮状结构组装过程中的一种中间聚合物。

An intermediate polymer in the assembly of clathrin baskets.

作者信息

Prasad K, Lippoldt R E, Edelhoch H, Lewis M S

出版信息

Biochemistry. 1986 Sep 9;25(18):5214-9. doi: 10.1021/bi00366a035.

Abstract

Clathrin (8 S) is known to polymerize into two varieties of basket structures (150 S or 300 S) under the normal buffer conditions [100 mM 2-(N-morpholino)ethanesulfonic acid (Mes), pH 5.9-6.7] used for the isolation of coated vesicles. However, it is now observed that under very low salt conditions (2 mM Mes, pH 5.9), it forms a homogeneous species with a sedimentation coefficient of 27 S. Increasing the salt concentration to 50 mM Mes completely converts all the 27S species into 150S baskets. Sedimentation equilibrium data show that this 27S species has a molecular weight that is 6 times that of the clathrin protomer and is the result of highly cooperative reversible self-association of the 8S protomer. Light-scattering studies show that the stabilities of 27S species and baskets (150 S or 300 S) are comparable. Fluorescent labeling of sulfhydryl groups with N-(1-anilinonaphthalenyl)maleimide indicates that the conformation of clathrin in 27S species and baskets (150 S or 300 S) is similar. Trypsin digestion reveals that in the 27S species clathrin has a conformation differing from that in both the 8S species and baskets.

摘要

已知在用于分离被膜小泡的正常缓冲条件(100 mM 2-(N-吗啉代)乙磺酸(Mes),pH 5.9 - 6.7)下,网格蛋白(8 S)会聚合成两种篮状结构(150 S或300 S)。然而,现在观察到在极低盐条件(2 mM Mes,pH 5.9)下,它会形成一种沉降系数为27 S的均匀物种。将盐浓度增加到50 mM Mes会使所有27 S物种完全转化为150 S篮状结构。沉降平衡数据表明,这种27 S物种的分子量是网格蛋白原聚体的6倍,是8 S原聚体高度协同可逆自缔合的结果。光散射研究表明,27 S物种和篮状结构(150 S或300 S)的稳定性相当。用N-(1-苯胺基萘基)马来酰亚胺对巯基进行荧光标记表明,27 S物种和篮状结构(150 S或300 S)中网格蛋白的构象相似。胰蛋白酶消化显示,在27 S物种中,网格蛋白的构象与8 S物种和篮状结构中的构象不同。

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