Calorimetric determination of base‐stacking enthalpies in double‐helical DNA molecules

Luis A. Marky, Kenneth J. Breslauer

Research output: Contribution to journalArticle

92 Citations (Scopus)

Abstract

Differential scanning calorimetry was used to directly determine the transition enthalpies accompanying the duplex‐to‐single‐strand transition of poly[d(AT)], poly(dA)·poly(dT), poly[d(AC)]·poly[d(TG)], and d(GCGCGC). The calorimetric data allow us to define the following average base‐stacking enthalpies: (Table presented) Comparison with published data on the corresponding RNA interactions reveals remarkably good agreement. By assuming transition enthalpies to result from the pairwise disruption of nearest‐neighbor stacking interactions, we used the enthalpy data listed above to predict the transition enthalpies for three oligomeric DNA duplexes. Excellent agreement was found between the predicted and the calorimetrically determined values.

Original languageEnglish (US)
Pages (from-to)2185-2194
Number of pages10
JournalBiopolymers
Volume21
Issue number11
DOIs
StatePublished - Nov 1982

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Differential Scanning Calorimetry
Enthalpy
DNA
RNA
Molecules
Differential scanning calorimetry
polydeoxyadenylic acid-polythymidylic acid

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Biomaterials
  • Organic Chemistry

Cite this

Calorimetric determination of base‐stacking enthalpies in double‐helical DNA molecules. / Marky, Luis A.; Breslauer, Kenneth J.

In: Biopolymers, Vol. 21, No. 11, 11.1982, p. 2185-2194.

Research output: Contribution to journalArticle

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