The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy

Kim J, Doose S, Neuweiler H, Sauer M (2006)
Nucleic Acids Research 34(9): 2516-2527.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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DOI
URN
urn:nbn:de:0070-pub-17738488
Autor*in
Kim, Jiho; Doose, Sören; Neuweiler, Hannes; Sauer, MarkusUniBi
Einrichtung
SFB 613 Physik von Einzelmolekülprozessen/mol.Erkennung in organ.Sys.
Fakultät für Physik
Abstract / Bemerkung
Conformational fluctuations of single-stranded DNA (ssDNA) oligonucleotides were studied in aqueous solution by monitoring contact-induced fluorescence quenching of the oxazine fluorophore MR121 by intrinsic guanosine residues (dG). We applied fluorescence correlation spectroscopy as well as steady-state and time-resolved fluorescence spectroscopy to analyze kinetics of DNA hairpin folding. We first characterized the reporter system by investigating bimolecular quenching interactions between MR121 and guanosine monophosphate in aqueous solution estimating rate constants, efficiency and stability for formation of quenched complexes. We then studied the kinetics of complex formation between MR121 and dG residues site-specifically incorporated in DNA hairpins. To uncover the initial steps of DNA hairpin folding we investigated complex formation in ssDNA carrying one or two complementary base pairs (dC–dG pairs) that could hybridize to form a short stem. Our data show that incorporation of a single dC–dG pair leads to non-exponential decays for opening and closing kinetics and reduces rate constants by one to two orders of magnitude. We found positive activation enthalpies independent of the number of dC–dG pairs. These results imply that the rate limiting step of DNA hairpin folding is not determined by loop dynamics, or by mismatches in the stem, but rather by interactions between stem and loop nucleotides.
Erscheinungsjahr
2006
Zeitschriftentitel
Nucleic Acids Research
Band
34
Ausgabe
9
Seite(n)
2516-2527
ISSN
0305-1048
eISSN
1362-4962
Page URI
https://pub.uni-bielefeld.de/record/1773848

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Kim J, Doose S, Neuweiler H, Sauer M. The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy. Nucleic Acids Research. 2006;34(9):2516-2527.
Kim, J., Doose, S., Neuweiler, H., & Sauer, M. (2006). The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy. Nucleic Acids Research, 34(9), 2516-2527. https://doi.org/10.1093/nar/gkl221
Kim, Jiho, Doose, Sören, Neuweiler, Hannes, and Sauer, Markus. 2006. “The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy”. Nucleic Acids Research 34 (9): 2516-2527.
Kim, J., Doose, S., Neuweiler, H., and Sauer, M. (2006). The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy. Nucleic Acids Research 34, 2516-2527.
Kim, J., et al., 2006. The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy. Nucleic Acids Research, 34(9), p 2516-2527.
J. Kim, et al., “The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy”, Nucleic Acids Research, vol. 34, 2006, pp. 2516-2527.
Kim, J., Doose, S., Neuweiler, H., Sauer, M.: The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy. Nucleic Acids Research. 34, 2516-2527 (2006).
Kim, Jiho, Doose, Sören, Neuweiler, Hannes, and Sauer, Markus. “The initial step of DNA hairpin folding: a kinetic analysis using fluorescence correlation spectroscopy”. Nucleic Acids Research 34.9 (2006): 2516-2527.
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