Premium
Comparison of DNA Complex Formation Behaviour for Two Closely Related Lexitropsin Analogues
Author(s) -
Parkinson John A.,
Khalaf Abedawn I.,
Anthony Nahoum G.,
MacKay Simon P.,
Suckling Colin J.,
Waigh Roger D.
Publication year - 2009
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.200800390
Subject(s) - chemistry , ligand (biochemistry) , dna , nuclear magnetic resonance spectroscopy , stereochemistry , crystallography , minor groove , biochemistry , receptor
Two closely related lexitropsin analogues that differ only in the form of the ‘headgroup’ functionality (CHO (for 1 ) vs. Ac (for 2 )) have been studied in their DNA‐binding capacity for the sequence d(GCATATATGC) using 1 H‐NMR spectroscopy. DNA‐Complex formation for the CHO derivative was apparent from the observation of new NMR signals on titration of DNA with ligand. Detailed investigation and assignment of the data for a ligand/DNA‐duplex ratio of 2 : 1 clearly delineated the structure as one associated with the ‘minor groove’ class of DNA complexes. The structure of the complex was determined on the basis of the acquired NMR data. Features characteristic of typical 2 : 1 minor‐groove complexes were apparent. In a similar experimental approach, the Ac analogue ligand–DNA binding response was investigated. Despite the close similarity in chemical structure to the CHO case, the Ac analogue was found to produce NMR data of a much poorer quality. This was attributed to more rapid on/off chemical exchange equilibrium between ligand and DNA. From close analysis and comparison of the NMR data for the ‘Ac’ and ‘CHO’ headgroup ligand–DNA complexes, it was possible to ascertain that the same type of complex formed in each case but with different relative binding constants. Consideration of the nature and form of these complexes has been made with reference to a previously determined structure from our laboratory for the related lexitropsin analogue thiazotropsin A.