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通过“转运特异性分级分离”对源自突触体的囊泡中的ATP依赖性钙转运成分进行重组和纯化。

Reconstitution and purification by "transport specificity fractionation" of an ATP-dependent calcium transport component from synaptosome-derived vesicles.

作者信息

Papazian D, Rahamimoff H, Goldin S M

出版信息

Proc Natl Acad Sci U S A. 1979 Aug;76(8):3708-12. doi: 10.1073/pnas.76.8.3708.

Abstract

A synaptosomal ATP-dependent Ca uptake system was reconstituted into artificial vesicles by a cholate dialysis procedure using an 80-fold excess of exogenous phospholipid. Under these conditions, most of these vesicles would be expected to have only one or, at most, a few membrane proteins. The vesicles containing an ATP-dependent Ca transport system were purified from the bulk of the preparation on density gradients by increasing their density by the ATP-dependent intravesicular precipitation of Ca oxalate; a approximately 100-fold purification resulted. The purified Ca-transporting vesicles contained two major protein components, of Mr 94,000 and 140,000 according to sodium dodecyl sulfate gel electrophoresis. These components are believed to be responsible for Ca transport in this synaptosome-derived membrane fraction.

摘要

通过胆酸盐透析程序,使用过量80倍的外源性磷脂,将突触体依赖ATP的钙摄取系统重构成人工囊泡。在这些条件下,预计大多数这些囊泡仅含有一种或至多几种膜蛋白。通过草酸钙的ATP依赖性囊泡内沉淀增加其密度,从大量制剂中通过密度梯度纯化含有ATP依赖性钙转运系统的囊泡;得到了约100倍的纯化。根据十二烷基硫酸钠凝胶电泳,纯化的钙转运囊泡含有两种主要蛋白质成分,分子量分别为94,000和140,000。据信这些成分负责该突触体衍生膜部分中的钙转运。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4db3/383902/f2cd9fa21108/pnas00008-0148-a.jpg

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