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A transposase strategy for creating libraries of circularly permuted proteins.

Abstract
A simple approach for creating libraries of circularly permuted proteins is described that is called PERMutation Using Transposase Engineering (PERMUTE). In PERMUTE, the transposase MuA is used to randomly insert a minitransposon that can function as a protein expression vector into a plasmid that contains the open reading frame (ORF) being permuted. A library of vectors that express different permuted variants of the ORF-encoded protein is created by: (i) using bacteria to select for target vectors that acquire an integrated minitransposon; (ii) excising the ensemble of ORFs that contain an integrated minitransposon from the selected vectors; and (iii) circularizing the ensemble of ORFs containing integrated minitransposons using intramolecular ligation. Construction of a Thermotoga neapolitana adenylate kinase (AK) library using PERMUTE revealed that this approach produces vectors that express circularly permuted proteins with distinct sequence diversity from existing methods. In addition, selection of this library for variants that complement the growth of Escherichia coli with a temperature-sensitive AK identified functional proteins with novel architectures, suggesting that PERMUTE will be useful for the directed evolution of proteins with new functions.
AuthorsManan M Mehta, Shirley Liu, Jonathan J Silberg
JournalNucleic acids research (Nucleic Acids Res) Vol. 40 Issue 9 Pg. e71 (May 2012) ISSN: 1362-4962 [Electronic] England
PMID22319214 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adenylate Kinase
  • Transposases
Topics
  • Adenylate Kinase (chemistry, genetics)
  • Escherichia coli (genetics)
  • Genetic Variation
  • Genetic Vectors
  • Mutagenesis, Insertional (methods)
  • Thermotoga neapolitana (enzymology)
  • Transposases

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