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. Author manuscript; available in PMC: 2009 Dec 28.
Published in final edited form as: Protein Eng Des Sel. 2005 Jun 24;18(7):309–319. doi: 10.1093/protein/gzi038

Fig. 1.

Fig. 1

In vitro selection scheme using mRNA display. The starting dsDNA pool (top, center) which encodes the peptide library is transcribed in vitro. Purified mRNA is enzymatically ligated to a puromycin-DNA oligo prior to RNA-peptide fusion formation via in vitro translation. Purified RNA-peptide fusions are reverse transcribed and affinity selected onto the immobilized antibody target. Eluted cDNA is used as the template for PCR for the next cycle of selection.