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移植和显微注射蛋白质的细胞内降解命运

Intracellular degradative fate of transplanted and microinjected proteins.

作者信息

Mayer R J, Russell S M, Amenta J S, Evans P J, Fernig D, Doherty F

出版信息

Prog Clin Biol Res. 1985;180:395-404.

PMID:3898110
Abstract

The mechanisms of intracellular protein catabolism have not been elucidated in spite of 42 years since Schoenheimer's treatise on "The Dynamic State of Body Constituents". Protein catabolism (cf. Protein Synthesis) involves multiple mechanisms, several of which occur reliably only in cells, not test-tubes. Elucidation of the mechanisms relies on both cell biological and enzymological approaches. Transplantation and microinjection of proteins into target cells, although naturally not without experimental and interpretive difficulties, provide the means of identifying the molecular and cell biological events in intracellular protein degradation. In short, these techniques provide the bioassay system to probe the functions of known catalysts and inhibitors of proteinolysis and provide the means of identifying the currently unknown features of the cytoplasmic surveillance system which present the protein substrates for destruction.

摘要

尽管自舍恩海默关于《身体成分的动态状态》的论文发表以来已有42年,但细胞内蛋白质分解代谢的机制仍未阐明。蛋白质分解代谢(参见蛋白质合成)涉及多种机制,其中一些机制仅在细胞中可靠地发生,而不在试管中发生。对这些机制的阐明依赖于细胞生物学和酶学方法。将蛋白质移植和显微注射到靶细胞中,尽管自然并非没有实验和解释上的困难,但提供了识别细胞内蛋白质降解中分子和细胞生物学事件的手段。简而言之,这些技术提供了生物测定系统,以探究已知的蛋白水解催化剂和抑制剂的功能,并提供了识别细胞质监测系统当前未知特征的手段,该系统为蛋白质底物的破坏提供条件。

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