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从酿酒酵母中分离天然可溶性和膜结合蛋白复合物

Isolation of Native Soluble and Membrane-Bound Protein Complexes from Yeast Saccharomyces cerevisiae.

作者信息

Hansen Tobias, Chan Anna, Schröter Thomas, Schwerter Daniel, Girzalsky Wolfgang, Erdmann Ralf

机构信息

Abteilung für Systembiochemie, Institut für Biochemie und Pathobiochemie, Medizinische Fakultät der Ruhr-Universität Bochum, Ruhr-Universität Bochum, Universitätsstr. 150, 44780, Bochum, Germany.

出版信息

Methods Mol Biol. 2017;1595:37-44. doi: 10.1007/978-1-4939-6937-1_4.

Abstract

Immunoprecipitation is a traditional approach to isolate single proteins or native protein complexes from a complex sample mixture. The original method makes use of specific antibodies against endogenous proteins or epitope tags, which are first bound to the target protein and then isolated with protein A beads. An advancement of this method is the application of a protein A tag fused to the target protein and the affinity-purification of the tagged protein with human Immunoglobulin G chemically cross-linked to a sepharose matrix. This method will be described exemplified by the purification of protein complexes of the peroxisomal membrane from yeast Saccharomyces cerevisiae.

摘要

免疫沉淀是一种从复杂样品混合物中分离单一蛋白质或天然蛋白质复合物的传统方法。原始方法利用针对内源性蛋白质或表位标签的特异性抗体,这些抗体首先与靶蛋白结合,然后用蛋白A磁珠进行分离。该方法的一个改进是将蛋白A标签融合到靶蛋白上,并用人免疫球蛋白G化学交联到琼脂糖基质上对标记蛋白进行亲和纯化。本文将以从酿酒酵母中纯化过氧化物酶体膜蛋白复合物为例描述该方法。

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