In vitro selection from protein and peptide libraries.

Abstract:

:In vitro selection from molecular libraries has rapidly come of age as a protein-engineering tool. Dramatic increases in protein affinity can be engineered using phage-display libraries, and specific antibodies can be selected directly from a single 'naïve' library of their genes. Repertoires of small molecules are a potentially valuable resource for drug discovery. Libraries of linear peptides provide ligands for proteins that recognize continuous epitopes, and low-affinity mimics of some small molecules, but generally do not contain mimics of large molecular interfaces. Switching to constrained peptide formats, and deploying more diverse, non-peptide chemical libraries, may bring greater success.

journal_name

Trends Biotechnol

journal_title

Trends in biotechnology

authors

Clackson T,Wells JA

doi

10.1016/0167-7799(94)90079-5

subject

Has Abstract

pub_date

1994-05-01 00:00:00

pages

173-84

issue

5

eissn

0167-7799

issn

1879-3096

pii

0167-7799(94)90079-5

journal_volume

12

pub_type

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