4.5 Article

An enhanced recombinant amino-terminal acetylation system and novel in vivo high-throughput screen for molecules affecting α-synuclein oligomerisation

期刊

FEBS LETTERS
卷 591, 期 6, 页码 833-841

出版社

WILEY
DOI: 10.1002/1873-3468.12597

关键词

amino-alpha-acetyl-transferase; Nat; Parkinson's disease; Tropomyosin; alpha-synuclein

资金

  1. Biotechnology and Biological Sciences Research Council [BB/K012045/1, BB/J012793/1]
  2. Leverhulme Early Career Fellowship [ECF-2013-341]
  3. Royal Society Industry Fellowship
  4. University of Kent
  5. Biotechnology and Biological Sciences Research Council [1213887, 1405589] Funding Source: researchfish

向作者/读者索取更多资源

Amino-terminal acetylation is a ubiquitous protein modification affecting the majority of eukaryote proteins to regulate stability and function. We describe an optimised recombinant expression system for rapid production of amino terminal-acetylated proteins within bacteria. We go on to describe the system's use in a fluorescence based in vivo assay for use in the high-throughput screen to identify drugs that impact amino-terminal acetylation-dependent oligomerisation. These new tools and protocols will allow researchers to enhance routine recombinant protein production and identify new molecules for use in research and clinical applications.

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