| Literature DB >> 27516170 |
Jean-Paul Renaud1,2,3, Chun-Wa Chung4, U Helena Danielson5,6, Ursula Egner7, Michael Hennig8,9, Roderick E Hubbard10,11, Herbert Nar12.
Abstract
Over the past 25 years, biophysical technologies such as X-ray crystallography, nuclear magnetic resonance spectroscopy, surface plasmon resonance spectroscopy and isothermal titration calorimetry have become key components of drug discovery platforms in many pharmaceutical companies and academic laboratories. There have been great improvements in the speed, sensitivity and range of possible measurements, providing high-resolution mechanistic, kinetic, thermodynamic and structural information on compound-target interactions. This Review provides a framework to understand this evolution by describing the key biophysical methods, the information they can provide and the ways in which they can be applied at different stages of the drug discovery process. We also discuss the challenges for current technologies and future opportunities to use biophysical methods to solve drug discovery problems.Mesh:
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Year: 2016 PMID: 27516170 DOI: 10.1038/nrd.2016.123
Source DB: PubMed Journal: Nat Rev Drug Discov ISSN: 1474-1776 Impact factor: 84.694