| Literature DB >> 28873270 |
Shan Tang1, Lu-Jun Liang1, Yan-Yan Si1, Shuai Gao1, Jia-Xing Wang1, Jun Liang2, Ziqing Mei3, Ji-Shen Zheng2, Lei Liu1.
Abstract
Chemical ubiquitination is an effective approach for accessing structurally defined, atypical ubiquitin (Ub) chains that are difficult to prepare by other techniques. Herein, we describe a strategy that uses a readily accessible premade isopeptide-linked 76-mer (isoUb), which has an N-terminal Cys and a C-terminal hydrazide, as the key building block to assemble atypical Ub chains in a modular fashion. This method avoids the use of auxiliary-modified Lys and instead employs the canonical and therefore more robust Cys-based native chemical ligation technique. The efficiency and capacity of this isoUb-based strategy is exemplified by the cost-effective synthesis of several linkage- and length-defined atypical Ub chains, including K27-linked tetra-Ub and K11/K48-branched tri-, tetra-, penta-, and hexa-Ubs.Entities:
Keywords: native chemical ligation; post-translational modifications; protein chemical synthesis; proteolysis; ubiquitin
Year: 2017 PMID: 28873270 DOI: 10.1002/anie.201708067
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336