DNA footprinting

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Ranking Ligand Affinity For The DNA Minor Groove By Experiment And Simulation

Journal Title, Volume, Page: 
American Chemical Society Med. Chem. Lett., 2010, 1 (8), pp 376–380 DOI: 10.1021/ml100047n
Year of Publication: 
2010
Authors: 
Hasan Y. Alniss
Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow G4 0NR, United Kingdom
Current Affiliation: 
Department of Pharmacy, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine
Simon P. MacKay
University of strathclyde, Glasgow, UK
John A. Parkinson
University of strathclyde, Glasgow, UK
Preferred Abstract (Original): 

The structural and thermodynamic basis for the strength and selectivity of the interactions of minor groove binders (MGBs) with DNA is not fully understood. In 2003, we reported the first example of a thiazole-containing MGB that bound in a phase-shifted pattern that spanned six base pairs rather than the usual four (for tricyclic distamycin-like compounds). Since then, using DNA footprinting, NMR spectroscopy, isothermal titration calorimetry, and molecular dynamics, we have established that the flanking bases around the central four being read by the ligand have subtle effects on recognition. We have investigated the effect of these flanking sequences on binding and the reasons for the differences and established a computational method to rank ligand affinity against varying DNA sequences.

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