Effect of locked nucleic acid modifications on the thermal stability of noncanonical DNA structure.

Biochemistry

FIBER (Frontier Institute for Biomolecular Engineering Research), Konan University, 7-1-20 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan.

Published: August 2011

AI Article Synopsis

  • The study investigated how locked nucleic acid (LNA) modifications influence the behavior of parallel and antiparallel DNA duplexes, specifically focusing on kinetic and thermodynamic effects.
  • LNA modifications significantly increased the association rate constants for parallel duplex formation while drastically decreasing the dissociation rate constants, indicating a much more stable structure compared to unmodified duplexes.
  • Thermodynamically, the LNA modifications provided greater stabilization to parallel duplexes (3.6 kcal/mol) versus antiparallel ones (1.6 kcal/mol), suggesting potential applications in designing advanced molecules for detecting DNA/RNA and creating molecular switches.

Article Abstract

We studied the kinetic and thermodynamic effects of locked nucleic acid (LNA) modifications on parallel and antiparallel DNA duplexes. The LNA modifications were introduced at cytosine bases of the pyrimidine strand. Kinetic parameters evaluated from melting and annealing curves showed that the association and dissociation rate constants for the formation of the LNA-modified parallel duplex at 25.0 °C were 3 orders of magnitude larger and 6 orders of magnitude smaller, respectively, than that of the unmodified parallel duplex. The activation energy evaluated from the temperature-dependent rate constants was largely altered by the LNA modifications, suggesting that the LNA modifications affected a prenucleation event in the folding process. Moreover, thermodynamic parameters showed that the extent of stabilization by the LNA modification for parallel duplexes (3.6 kcal mol(-1) per one modification) was much more significant than that of antiparallel duplexes (1.6 kcal mol(-1)). This large stabilization was due to the decrease in ΔH° that was more favorable than the decrease in TΔS°. These quantitative parameters demonstrated that LNA modification specifically stabilized the noncanonical parallel duplex. On the basis of these observations, we succeeded to stabilize the parallel duplex by LNA modification at the physiological pH. These results can be useful in the rational design of functional molecules such as more effective antisense and antigene strands, more sensitive strands for detection of target DNA and RNA strands, and molecular switches responding to solution pH.

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http://dx.doi.org/10.1021/bi200477gDOI Listing

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