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Solution Structure of a DNA Duplex Containing a Biphenyl Pair
Author(s) -
Johar Zeena,
Zahn Alain,
Leumann Christian J.,
Jaun Bernhard
Publication year - 2008
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200701304
Subject(s) - stacking , biphenyl , nucleobase , hydrogen bond , duplex (building) , base pair , intercalation (chemistry) , chemistry , crystallography , van der waals force , dna , stereochemistry , molecule , organic chemistry , biochemistry
Hydrogen‐bonding and stacking interactions between nucleobases are considered to be the major noncovalent interactions that stabilize the DNA and RNA double helices. In recent work we found that one or multiple biphenyl pairs, devoid of any potential for hydrogen bond formation, can be introduced into a DNA double helix without loss of duplex stability. We hypothesized that interstrand stacking interactions of the biphenyl residues maintain duplex stability. Here we present an NMR structure of the decamer duplex d(GTGACXGCAG)⋅ d(CTGCYGTCAC) that contains one such X/Y biaryl pair. X represents a 3′′,5′′‐dinitrobiphenyl‐ and Y a 3′′,4′′‐dimethoxybiphenyl C ‐nucleoside unit. The experimentally determined solution structure shows a B‐DNA duplex with a slight kink at the site of modification. The biphenyl groups are intercalated side by side as a pair between the natural base pairs and are stacked head to tail in van der Waals contact with each other. The first phenyl rings of the biphenyl units each show tight intrastrand stacking to their natural base neighbors on the 3′‐side, thus strongly favoring one of two possible interstrand intercalation structures. In order to accommodate the biphenyl units in the duplex the helical pitch is widened while the helical twist at the site of modification is reduced. Interestingly, the biphenyl rings are not static in the duplex but are in dynamic motion even at 294 K.