Abstract
A general method is described for creating chimeric proteins by transposition of subdomain-sized gene fragments. The method uses three sequential PCR steps to circumvent several limitations inherent in transposition of small insertions and has been optimized to avoid purification of intermediate products. The sequence-independence of the method permits flexibility in the choice of host molecule and insertion site.
Original language | English (US) |
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Pages (from-to) | 1099-1100 |
Number of pages | 2 |
Journal | Protein Engineering |
Volume | 10 |
Issue number | 9 |
DOIs | |
State | Published - 1997 |
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Biochemistry
Keywords
- Chimeric proteins
- PCR
- Protein structure
- Protein subdomains
- WrbA