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细胞因子调节的蛋白酶体活性评估。

Assessment of cytokine-modulated proteasome activity.

作者信息

Kirk Christopher J, Powell Saul R, Miller Edmund J

机构信息

Onyx Pharmaceuticals, 249 Grand Avenue South, San Francisco, CA, 94080, USA.

出版信息

Methods Mol Biol. 2014;1172:147-62. doi: 10.1007/978-1-4939-0928-5_13.

Abstract

This chapter presents two methods for assessment of proteasome function. The first is a modification of the standard fluorogenic peptide cleavage assay which takes into account the effect of ATP on proteasome activity. This method is described in both its macro and high throughput micro-assay forms. The second is the Proteasome Constitutive Immuno-Subunit (active site) ELISA or ProCISE method. ProCISE is a modification of active site directed probe analysis and allows for convenient differentiation between active constitutive and immuno-subunits. While the utility of measuring proteasome activity and its relationship to cytokine action and inflammation are clear, the assessment and interpretation is not always straightforward. Therefore, we also discuss the pitfalls of the standard fluorogenic assay, particularly in the interpretation of results obtained, and the advantages of the newer, ProCISE assay.

摘要

本章介绍了两种评估蛋白酶体功能的方法。第一种方法是对标准荧光肽切割试验的改进,该试验考虑了ATP对蛋白酶体活性的影响。此方法以宏观和高通量微量试验两种形式进行了描述。第二种方法是蛋白酶体组成性免疫亚基(活性位点)酶联免疫吸附测定法(ProCISE)。ProCISE是活性位点定向探针分析的一种改进方法,能够方便地区分活性组成性亚基和免疫亚基。虽然测量蛋白酶体活性及其与细胞因子作用和炎症之间关系的实用性是明确的,但评估和解释并不总是直截了当的。因此,我们还讨论了标准荧光测定法的缺陷,特别是在对所得结果的解释方面,以及较新的ProCISE测定法的优点。

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