Using Fragment-Based Technologies to Target Protein-Protein Interactions

Author(s): Justin F. Bower, Andrew Pannifer

Journal Name: Current Pharmaceutical Design

Volume 18 , Issue 30 , 2012

Become EABM
Become Reviewer
Call for Editor


Whilst fragment-based screening has found significant utility in aiding the discovery of high quality hits against a range of targets, the use of this technology in the protein-protein interaction inhibitor field is very much in its infancy. This review aims to highlight the key technologies used to identify fragment hits, such as NMR, SPR, X-ray crystallography and biochemical screening, the fragmentbased protein-protein interaction case studies reported to date and, more importantly, the potential of this methodology in unearthing high quality hit molecules in this critical area of drug discovery. In addition, we also discuss some of the key aspects of fragment library design, the composition of a high quality library and suggest ways in which future, more structurally diverse fragments which occupy different regions of chemical space to the vast majority of current fragment libraries may be selected.

Keywords: Fragment-based drug discovery, protein-protein interactions, hot spots, ligand efficiency, biophysical, techniques, inhibitors, fragment libraries, diversity, NMR.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2012
Published on: 23 August, 2012
Page: [4685 - 4696]
Pages: 12
DOI: 10.2174/138161212802651689
Price: $65

Article Metrics

PDF: 59