Journal
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume 327, Issue 1, Pages 49-56Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2004.11.137
Keywords
i-motif; NM23-H2; hysteresis; surface plasmon resonance; BIAcore; hybridization kinetics
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The nuclease hypersensitive element NHE III1 is an important anti-cancer target as the transcription of oncogene c-myc is largely regulated by it. It has been postulated that regulatory control is mediated by G-quadruplex formation in the NHE anti-sense strand through a competition between the duplex and the quadruplex states. A mutation in the NHE has been implicated in cancer. In this study, the reported mutation has been characterized vis-a-vis the kinetics of i-tetraplex formation (in the sense strand) and its effect on duplex formation. We found that i-tetraplex formation was destabilized by similar to1.4 kcal/mol (DeltaDeltaG at 20 degreesC, pH 5.8). Observed hysteresis allowed us to analyze the kinetics of folding for the mutant (M3). Though we observed higher association (DeltaE(on) approximate to -23.4 kcal/mol) and dissociation (DeltaE(off) approximate to 22.1 kcal/mol) activation energies (at pH 5.3) for the wild-type (P1) tetraplex folding, the kinetics of folding and unfolding for M3 was somewhat faster at pH 5.3 and 5.8. Interestingly, Surface plasmon resonance (BIAcore) analysis of hybridization at pH 6.6 indicated a higher association constant for M3 (similar to22.5 x 10(4) M-1 s(-1)) than P1 (similar to3.2 x 10(4) M-1 s(-1)). The equilibrium dissociation constants also indicated favorable duplex association for M3 (similar to22.2 and similar to190.6 nM for M3 and P1, respectively). We envisage that the increased affinity for the duplex state due to the mutation could play a functional role in the aberrant regulation of c-myc. (C) 2004 Elsevier Inc. All rights reserved.
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