Hydrogen Bond Mediated Association of Dinucleotide Analogs

Verfasser / Beitragende:
[Eline M. Basílio Janke, Klaus Weisz]
Ort, Verlag, Jahr:
2003
Enthalten in:
Zeitschrift für Physikalische Chemie/International journal of research in physical chemistry and chemical physics, 217/12/2003(2003-12-01), 1463-1472
Format:
Artikel (online)
ID: 378862839
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024 7 0 |a 10.1524/zpch.217.12.1463.20475  |2 doi 
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245 0 0 |a Hydrogen Bond Mediated Association of Dinucleotide Analogs  |h [Elektronische Daten]  |c [Eline M. Basílio Janke, Klaus Weisz] 
520 3 |a Several dinucleotide analogs, in which two of the nucleobases adenine, thymine and uracil are connected by a hexadecamethylene linker have been synthesized and studied for their base-base interaction in a chloroform solution. Using 1H NMR spectroscopic techniques intramolecular base pair formation through hydrogen bonding is observed at ambient temperatures but found to strongly depend on the identity of paired bases. Thus, whereas cyclization through intramolecular base-base interactions predominate for adenine-(CH2)16-thymine and adenine-(CH2)16-uracil, no intramolecular adenine-adenine pairing was observed. Upon addition of acetic acid to adenine-(CH2)16-thymine, strong adenine-acetic acid interactions result in the disruption of preformed intramolecular adenine-thymine base pairs. 
540 |a © 2003 Oldenbourg Wissenschaftsverlag GmbH 
690 7 |a Thermodynamics & statistical physics  |2 nationallicence 
690 7 |a Laboratory techniques, experiments  |2 nationallicence 
690 7 |a Physical chemistry  |2 nationallicence 
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700 1 |a Weisz  |D Klaus  |4 aut 
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