Source:http://linkedlifedata.com/resource/pubmed/id/20012417
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2009-12-16
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pubmed:abstractText |
The potential importance of G-quadruplex structures was implied by the recent findings that the human POT1 disrupts G-quadruplex and stimulates the telomerase activity. A solid understanding of the range of conformations that can be adopted by guanine-rich sequences can potentially shed much light on the molecular mechanisms underlying certain human diseases related to telomeres. Furthermore, structure-based design of chemotherapeutic drugs for cancer might be realized by addressing different types of G-quadruplex structures. Using the unique capabilities of single-molecule spectroscopy, we have recently reported on the intricate dynamic structural properties of a minimal form of human telomeric DNA. Here, we present the detailed step-by-step methods for the real-time observation of G-rich DNA sequences by means of single-molecule FRET microscopy and provide the protocols for vesicle encapsulation and surface immobilization assays. Such assays provide a firm basis for future studies aimed at elucidating the interaction between telomeric DNA and telomere-associated proteins as well as the synthetic therapeutic agents that specifically stabilize certain G-quadruplex topologies.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1940-6029
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
608
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
81-96
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
Real-time observation of G-quadruplex dynamics using single-molecule FRET microscopy.
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pubmed:affiliation |
Department of Physics, University of Illinois at Urbana Champaign, Urbana, IL, USA.
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pubmed:publicationType |
Journal Article
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