Premium
Enantioselective Proteins: Selection, Binding Studies and Molecular Modeling of Antibodies with Affinity towards Hydrophobic BINOL Derivatives
Author(s) -
Rasmussen Brian Schou,
Pedersen Jan Mondrup,
Sørensen Jesper,
Egebjerg Janni,
Schiøtt Birgit,
Mortensen Kim Kusk,
Skrydstrup Troels
Publication year - 2007
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.200700295
Subject(s) - hapten , chemistry , enantioselective synthesis , enantiomer , ligand (biochemistry) , combinatorial chemistry , phage display , hydrophobic effect , docking (animal) , stereochemistry , homology modeling , molecular model , antibody , catalysis , biochemistry , peptide , enzyme , biology , receptor , genetics , medicine , nursing
Abstract In this paper, the initial steps towards the design of novel artificial metalloenzymes that exploit proteins as a second coordination sphere for traditional metal–ligand catalysis are described. Phage display was employed to select and study antibody fragments capable of recognizing hydrophobic BINOL derivatives designed to mimic BINAP, a widely used ligand in asymmetric metal‐catalyzed reactions. The binding affinities of the selected antibodies towards a series of haptens were evaluated by using ELISA assays. A homology model of one of the most selective antibodies was constructed, and a computer‐assisted ligand‐docking study was carried out to elucidate the binding of the hapten. It was shown that, due to the hydrophobic nature of the haptens, a higher level of theoretical treatment was required to identify the correct binding modes. A small selection of the antibodies was found to discriminate between enantiomers and small structural modifications of the BINOL derivatives. The selectivities arise from hydrophobic interactions, and we propose that the identified set of antibodies provides a foundation for a novel route to artificial metalloenzymes.