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连接泛素的缺失环节:多聚泛素链的酶促生产方法。

The missing links to link ubiquitin: Methods for the enzymatic production of polyubiquitin chains.

作者信息

Faggiano Serena, Alfano Caterina, Pastore Annalisa

机构信息

Department of Pharmacy, University of Parma, 43124 Parma, Italy.

Maurice Wohl Institute, King's College London, 5 Cutcombe Rd, London SE5 9RX, United Kingdom.

出版信息

Anal Biochem. 2016 Jan 1;492:82-90. doi: 10.1016/j.ab.2015.09.013. Epub 2015 Oct 20.

Abstract

Attachment of ubiquitin (Ub) as monoUb and polyUb chains of different lengths and linkages to proteins plays a dominant role in very different regulatory mechanisms. Therefore, the study of polyUb chains has assumed a central interest in biochemistry and structural biology. An essential step necessary to allow in vitro biochemical and structural studies of polyUbs is the production of their chains in high quantities and purity. This is not always an easy task and can be achieved both enzymatically and chemically. Previous reviews have covered chemical cross-linking exhaustively. In this review, we concentrate on the different approaches developed so far for the enzymatic production of different Ub chains. These strategies permit a certain flexibility in the production of chains with various linkages and lengths. We critically describe the available methods and comment on advantages and limitations. It is clear that the field is mature to study most of the possible links, but some more work needs to be done to complete the picture and to exploit the current methodologies for understanding in full the Ub code.

摘要

泛素(Ub)以单泛素和不同长度及连接方式的多聚泛素链形式附着于蛋白质,在多种截然不同的调节机制中发挥着主导作用。因此,多聚泛素链的研究已成为生物化学和结构生物学的核心关注点。实现多聚泛素体外生化和结构研究的一个必要关键步骤,是大量且纯质地生产它们的链。这并非总是易事,可通过酶法和化学法实现。以往的综述已详尽涵盖化学交联。在本综述中,我们聚焦于迄今为酶法生产不同泛素链所开发的不同方法。这些策略在生产具有各种连接方式和长度的链时具有一定灵活性。我们批判性地描述现有方法,并对其优缺点进行评论。显然,该领域已成熟到足以研究大多数可能的连接方式,但仍需开展更多工作以完善全貌,并利用现有方法充分理解泛素密码。

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