Conformational Dynamics of Strand Register Shifts in DNA G‑Quadruplexes

The complex folding energy landscape of DNA G-quadruplexes leads to numerous conformations for this functionally important class of noncanonical DNA structures. A new layer of conformational heterogeneity comes from sequences with different numbers of G-nucleotides in each of the DNA G-strands that...

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Veröffentlicht in:Journal of the American Chemical Society 2020-01, Vol.142 (1), p.264-273
Hauptverfasser: Grün, J. Tassilo, Hennecker, Christopher, Klötzner, Dean-Paulos, Harkness, Robert W, Bessi, Irene, Heckel, Alexander, Mittermaier, Anthony K, Schwalbe, Harald
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Sprache:eng
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Zusammenfassung:The complex folding energy landscape of DNA G-quadruplexes leads to numerous conformations for this functionally important class of noncanonical DNA structures. A new layer of conformational heterogeneity comes from sequences with different numbers of G-nucleotides in each of the DNA G-strands that form the four-stranded G-quartet core. The mechanisms by which G-quadruplexes transition from one folded conformation to another are currently unknown. To address this question, we studied two different G-quadruplexes, selecting a single conformation by blocking hydrogen bonding with photolabile protection groups. Upon irradiation, the block can be released and the kinetics of re-equilibration to the native conformational equilibrium can be determined by time-resolved NMR. We compared the NMR-derived refolding kinetics with data derived from thermal hysteresis folding kinetic experiments and found excellent agreement. The outlined methodological approach allows separation of K+-induced G-quadruplex formation and subsequent refolding and provides key insight into rate-limiting steps of G-quadruplex conformational dynamics.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.9b10367