Libraries of hybrid proteins from distantly related sequences
Abstract
We introduce a method for sequence homology–independent protein recombination (SHIPREC) that can create libraries of single-crossover hybrids of unrelated or distantly related proteins. The method maintains the proper sequence alignment between the parents and introduces crossovers mainly at structurally related sites distributed over the aligned sequences. We used SHIPREC to create a library of interspecies hybrids of a membrane-associated human cytochrome P450 (1A2) and the heme domain of a soluble bacterial P450 (BM3). By fusing the hybrid gene library to the gene for chloramphenicol acetyl transferase (CAT), we were able to select for soluble and properly folded protein variants. Screening for 1A2 activity (deethylation of 7-ethoxyresorufin) identified two functional P450 hybrids that were more soluble in the bacterial cytoplasm than the wild-type 1A2 enzyme.
Additional Information
© 2001 Nature Publishing Group. Received 21 November 2000; Accepted 31 January 2001; Published 01 May 2001. V.S. was supported by a research fellowship from the Deutsche Forschungsgemeinschaft (DGF). This work was funded by Maxygen Inc.Additional details
- Eprint ID
- 90875
- DOI
- 10.1038/88129
- Resolver ID
- CaltechAUTHORS:20181113-135322855
- Deutsche Forschungsgemeinschaft (DFG)
- Maxygen Inc.
- Created
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2018-11-13Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field