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小牛胰酶原颗粒膜的大规模纯化

Large-scale purification of calf pancreatic zymogen granule membranes.

作者信息

Thévenod F, Haase W, Hopfer U

机构信息

Department of Physiology and Biophysics, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106.

出版信息

Anal Biochem. 1992 Apr;202(1):54-60. doi: 10.1016/0003-2697(92)90205-l.

Abstract

A protocol for isolating milligram quantities of highly purified zymogen granule membranes from calf pancreas was developed. The method provides a fivefold enriched zymogen granule fraction that is virtually free from major isodense contaminants, such as mitochondria and erythrocytes. Isolated granules are osmotically stable in isosmotic KCl buffers with half-lives between 90 and 120 min. They display specific ion permeabilities that can be demonstrated using ionophore probes to override intrinsic control mechanisms. A Cl- conductance, a Cl-/anion exchanger, and a K+ conductance are found in the zymogen granule membrane, as previously reported for rat pancreatic, rat parotid zymogen granules, and rabbit pepsinogen granules. Lysis of calf pancreatic secretory granules in hypotonic buffers and subsequent isolation of pure zymogen granule membranes yield about 5-10 mg membrane protein from approximately 1000 ml pancreas homogenate. The purified zymogen granule membranes are a putative candidate for the rapid identification and purification of epithelial Cl- channels and regulatory proteins, since they contain fewer proteins than plasma membranes.

摘要

已开发出一种从牛胰脏中分离毫克量高纯度酶原颗粒膜的方案。该方法提供了一个富集了五倍的酶原颗粒级分,几乎不含主要的等密度污染物,如线粒体和红细胞。分离出的颗粒在等渗KCl缓冲液中具有渗透压稳定性,半衰期在90至120分钟之间。它们表现出特定的离子通透性,这可以通过使用离子载体探针来超越内在控制机制来证明。如先前对大鼠胰腺、大鼠腮腺酶原颗粒和兔胃蛋白酶原颗粒所报道的那样,在酶原颗粒膜中发现了Cl-电导、Cl-/阴离子交换体和K+电导。在低渗缓冲液中裂解牛胰分泌颗粒,随后分离纯酶原颗粒膜,从大约1000毫升胰腺匀浆中可得到约5-10毫克膜蛋白。纯化的酶原颗粒膜是快速鉴定和纯化上皮Cl-通道及调节蛋白的一个假定候选物,因为它们所含的蛋白质比质膜少。

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