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靶向泛素共轭/去共轭机制特定组分的策略。

Strategies to Target Specific Components of the Ubiquitin Conjugation/Deconjugation Machinery.

作者信息

Taylor Neil C, McGouran Joanna F

机构信息

School of Chemistry and Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.

出版信息

Front Chem. 2020 Jan 10;7:914. doi: 10.3389/fchem.2019.00914. eCollection 2019.

Abstract

The regulation of ubiquitination status in the cell is controlled by ubiquitin ligases acting in tandem with deubiquitinating enzymes. Ubiquitination controls many key processes in the cell from division to death making its tight regulation key to optimal cell function. Activity based protein profiling has emerged as a powerful technique to study these important enzymes. With around 100 deubiquitinating enzymes and 600 ubiquitin ligases in the human genome targeting a subclass of these enzymes or even a single enzyme is a compelling strategy to unpick this complex system. In this review we will discuss different approaches adopted, including activity-based probes centered around ubiquitin-protein, ubiquitin-peptide and mutated ubiquitin scaffolds. We examine challenges faced and opportunities presented to increase specificity in activity-based protein profiling of the ubiquitin conjugation/deconjugation machinery.

摘要

细胞中泛素化状态的调节由与去泛素化酶协同作用的泛素连接酶控制。泛素化控制着细胞中从分裂到死亡的许多关键过程,因此其严格调控是细胞最佳功能的关键。基于活性的蛋白质谱分析已成为研究这些重要酶的强大技术。人类基因组中约有100种去泛素化酶和600种泛素连接酶,针对这些酶的一个亚类甚至单一酶进行研究是解析这个复杂系统的一个极具吸引力的策略。在本综述中,我们将讨论所采用的不同方法,包括围绕泛素-蛋白质、泛素-肽和突变泛素支架的基于活性的探针。我们审视了在泛素缀合/去缀合机制的基于活性的蛋白质谱分析中提高特异性所面临的挑战和机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a7/6966607/2d2a3a6339b1/fchem-07-00914-g0001.jpg

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