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Examination of the Deubiquitylation Site Selectivity of USP51 by Using Chemically Synthesized Ubiquitylated Histones
ChemBioChem ( IF 2.6 ) Pub Date : 2018-11-21 , DOI: 10.1002/cbic.201800432 Huasong Ai 1 , Yu Guo 2, 3 , Demeng Sun 4 , Sanling Liu 4 , Yunkun Qi 1 , Jing Guo 1 , Qian Qu 1 , Qingyue Gong 4 , Suwen Zhao 2 , Jiabin Li 4 , Lei Liu 1
ChemBioChem ( IF 2.6 ) Pub Date : 2018-11-21 , DOI: 10.1002/cbic.201800432 Huasong Ai 1 , Yu Guo 2, 3 , Demeng Sun 4 , Sanling Liu 4 , Yunkun Qi 1 , Jing Guo 1 , Qian Qu 1 , Qingyue Gong 4 , Suwen Zhao 2 , Jiabin Li 4 , Lei Liu 1
Affiliation
Nicking nucleosomes: Five ubiquitylated histones are synthesized through chemical total synthesis and reconstituted to nucleosomes. These histones are used to examine the deubiquitylation selectivity of USP51. Results indicate that USP51 cleaves the surface‐ubiquitylated nucleosomes, but is inactive against ubiquitin embedded inside the nucleosome.
中文翻译:
通过使用化学合成的泛素化组蛋白检查USP51的去泛素化位点选择性
切开核小体:通过化学全合成合成五个泛素化的组蛋白,然后重组为核小体。这些组蛋白用于检查USP51的去泛素化选择性。结果表明,USP51裂解表面泛素化的核小体,但对嵌入核小体中的泛素无活性。
更新日期:2018-11-21
中文翻译:
通过使用化学合成的泛素化组蛋白检查USP51的去泛素化位点选择性
切开核小体:通过化学全合成合成五个泛素化的组蛋白,然后重组为核小体。这些组蛋白用于检查USP51的去泛素化选择性。结果表明,USP51裂解表面泛素化的核小体,但对嵌入核小体中的泛素无活性。