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Digitale Medien

Use of organic solvents and small molecules for locating binding sites on proteins in solution* (1999)

Dalvit, Claudio ; Floersheim, Philipp ; Zurini, Mauro ; [weitere]

Springer

Journal of biomolecular NMR 14 (1999), S. 23-32

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ISSN: 1573-5001

Schlagwort(e): FK506 binding protein ; multiple solvent suppression ; organic solvents ; protein–ligand interactions ; 3D NMR structure

Quelle: Springer Online Journal Archives 1860-2000

Thema: Biologie , Chemie und Pharmazie

Notizen: Abstract Application of a modified ePHOGSY and other novel NMR experiments to an H2O-DMSO solution of the protein FKBP12 identified the presence of one molecule of DMSO bound in the substrate binding site. It occupies the same spatial region occupied by the pipecolidine moiety of the immunosuppressive drugs FK506 and Rapamycin complexed to the protein. The binding constant KD for this DMSO molecule was only 275 mM. A substructure search of small molecules similar to DMSO resulted in the identification of molecules with improved binding affinity. This work represents a clear example of the powerful interplay of molecular modelling and NMR.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1023/A:1008378929578

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