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.

Keywords

BiologyTransposaseORFSOpen reading frameGeneticsComputational biologyPlasmidPeptide sequenceTransposable elementDNAGeneGenome

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Year
2012
Type
article
Volume
40
Issue
9
Pages
e71-e71
Citations
1055
Access
Closed

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Manan Mehta, Shirley Liu, Jonathan J. Silberg (2012). A transposase strategy for creating libraries of circularly permuted proteins. Nucleic Acids Research , 40 (9) , e71-e71. https://doi.org/10.1093/nar/gks060

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DOI
10.1093/nar/gks060