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J Med Chem. 2016 Mar 10;59(5):2192-204. doi: 10.1021/acs.jmedchem.5b01940. Epub 2016 Feb 29.

Native State Mass Spectrometry, Surface Plasmon Resonance, and X-ray Crystallography Correlate Strongly as a Fragment Screening Combination.

Author information

1
Griffith University , Eskitis Institute for Drug Discovery, Brisbane, Queensland Australia.
2
CSIRO Biomedical Manufacturing Program, Melbourne, Victoria Australia.

Abstract

Fragment-based drug discovery (FBDD) is contingent on the development of analytical methods to identify weak protein-fragment noncovalent interactions. Herein we have combined an underutilized fragment screening method, native state mass spectrometry, together with two proven and popular fragment screening methods, surface plasmon resonance and X-ray crystallography, in a fragment screening campaign against human carbonic anhydrase II (CA II). In an initial fragment screen against a 720-member fragment library (the "CSIRO Fragment Library") seven CA II binding fragments, including a selection of nonclassical CA II binding chemotypes, were identified. A further 70 compounds that comprised the initial hit chemotypes were subsequently sourced from the full CSIRO compound collection and screened. The fragment results were extremely well correlated across the three methods. Our findings demonstrate that there is a tremendous opportunity to apply native state mass spectrometry as a complementary fragment screening method to accelerate drug discovery.

PMID:
26882437
DOI:
10.1021/acs.jmedchem.5b01940
[Indexed for MEDLINE]

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