Identification of metal ion binding peptides containing unnatural amino acids by phage display

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The bidentate metal binding amino acid bipyridylalanine (BpyAla) was incorporated into a disulfide linked cyclic peptide phage displayed library to identify metal ion binding peptides. Selection against Ni2+-nitrilotriacetic acid (NTA) enriched for sequences containing histidine and BpyAla. BpyAla predominated when selections were carried out at lower pH, consistent with the differential pK(a)'s of histidine and BpyAla. Two peptides containing BpyAla were synthesized and found to bind Ni2+ with low micromolar dissociation constants. Incorporation of BpyAla and other metal binding amino acids into peptide and protein libraries should enable the evolution of novel binding and catalytic activities. (C) 2013 Published by Elsevier Ltd.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
2013-05
Language
English
Article Type
Article
Keywords

DESIGN; METALLOPROTEINS; PROTEINS; EVOLUTION

Citation

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.23, no.9, pp.2598 - 2600

ISSN
0960-894X
DOI
10.1016/j.bmcl.2013.02.106
URI
http://hdl.handle.net/10203/209137
Appears in Collection
BS-Journal Papers(저널논문)
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