Traceless protein splicing utilizing evolved split inteins

Steve W. Lockless, Tom W. Muir

Research output: Contribution to journalArticle

78 Scopus citations

Abstract

Split inteins are parasitic genetic elements frequently found inserted into reading frames of essential proteins. Their association and excision restore host protein function through a protein self-splicing reaction. They have gained an increasingly important role in the chemical modification of proteins to create cyclical, segmentally labeled, and fluorescently tagged proteins. Ideally, inteins would seamlessly splice polypeptides together with no remnant sequences and at high efficiency. Here, we describe experiments that identify the branched intermediate, a transient step in the overall splicing reaction, as a key determinant of the splicing efficiency at different splice-site junctions. To alter intein specificity, we developed a cellbased selection scheme to evolve split inteins that splice with high efficiency at different splice junctions and at higher temperatures. Mutations within these evolved inteins occur at sites distant from the active site. We present a hypothesis that a network of conserved coevolving amino acids in inteins mediates these long-range effects.

Original languageEnglish (US)
Pages (from-to)10999-11004
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume106
Issue number27
DOIs
StatePublished - Jul 7 2009
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General

Keywords

  • Coevolution
  • Crk-II
  • Directed evolution
  • Protein ligation
  • SCA

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