The emergence of a relatively new technique resulting from a combination of frontal affinity chromatography coupled with MS detection (FAC-MS) has extended the capabilities of MS in drug discovery and development. Its application in a broad range of biological systems, together with its label-free operation, relatively high throughput, ability to rank ligands and determine K-d, makes FAC-MS a universal tool enabling convenient and efficient screening in the identification of new potential drug leads. Here we will highlight FAC-MS screening studies and discuss where it can be applied in evaluating multiple protein-binding sites, protein-protein interactions and inactive proteins, and also in determining selectivity.
机构:
GlaxoSmithKline, Platform Technol & Sci, Drug Metab & Pharmacokinet, King Of Prussia, PA 19406 USAGlaxoSmithKline, Platform Technol & Sci, Drug Metab & Pharmacokinet, King Of Prussia, PA 19406 USA
Kellie, John
Szapacs, Matthew
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机构:
GlaxoSmithKline, Platform Technol & Sci, Drug Metab & Pharmacokinet, King Of Prussia, PA 19406 USAGlaxoSmithKline, Platform Technol & Sci, Drug Metab & Pharmacokinet, King Of Prussia, PA 19406 USA