Stability of human telomere quadruplexes at high DNA concentrations
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24037480
DOI
10.1002/bip.22400
Knihovny.cz E-resources
- Keywords
- DNA concentration, circular dichroism, folding topology, quadruplex, thermal and thermodynamic stability,
- MeSH
- Circular Dichroism MeSH
- Densitometry MeSH
- DNA chemistry MeSH
- Electrophoresis, Polyacrylamide Gel MeSH
- Entropy MeSH
- G-Quadruplexes * MeSH
- Humans MeSH
- Microscopy, Atomic Force MeSH
- Spectrophotometry, Ultraviolet MeSH
- Telomere chemistry MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA MeSH
For mimicking macromolecular crowding of DNA quadruplexes, various crowding agents have been used, typically PEG, with quadruplexes of micromolar strand concentrations. Thermal and thermodynamic stabilities of these quadruplexes increased with the concentration of the agents, the rise depended on the crowder used. A different phenomenon was observed, and is presented in this article, when the crowder was the quadruplex itself. With DNA strand concentrations ranging from 3 µM to 9 mM, the thermostability did not change up to ∼2 mM, above which it increased, indicating that the unfolding quadruplex units were not monomolecular above ∼2 mM. The results are explained by self-association of the G-quadruplexes above this concentration. The ΔG(°) 37 values, evaluated only below 2 mM, did not become more negative, as with the non-DNA crowders, instead, slightly increased. Folding topology changed from antiparallel to hybrid above 2 mM, and then to parallel quadruplexes at high, 6-9 mM strand concentrations. In this range, the concentration of the DNA phosphate anions approached the concentration of the K(+) counterions used. Volume exclusion is assumed to promote the topological changes of quadruplexes toward the parallel, and the decreased screening of anions could affect their stability.
References provided by Crossref.org
Loss of loop adenines alters human telomere d[AG3(TTAG3)3] quadruplex folding
DNA and RNA quadruplex-binding proteins