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Engineering the serpin α1-antitrypsin: A diversity of goals and techniques

期刊

PROTEIN SCIENCE
卷 29, 期 4, 页码 856-871

出版社

WILEY
DOI: 10.1002/pro.3794

关键词

protein design; protein engineering; proteinase inhibitor; serpin; alpha(1)-antitrypsin; alpha(1)-proteinase inhibitor

资金

  1. Canadian Blood Services [WS-IG2019]
  2. Heart and Stroke Foundation of Canada [G-19-0026318]

向作者/读者索取更多资源

alpha(1)-Antitrypsin (alpha(1)-AT) serves as an archetypal example for the serine proteinase inhibitor (serpin) protein family and has been used as a scaffold for protein engineering for >35 years. Techniques used to engineer alpha(1)-AT include targeted mutagenesis, protein fusions, phage display, glycoengineering, and consensus protein design. The goals of engineering have also been diverse, ranging from understanding serpin structure-function relationships, to the design of more potent or more specific proteinase inhibitors with potential therapeutic relevance. Here we summarize the history of these protein engineering efforts, describing the techniques applied to engineer alpha(1)-AT, specific mutants of interest, and providing an appended catalog of the >200 alpha(1)-AT mutants published to date.

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