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Volumn 9, Issue 24, 2011, Pages 8313-8320

Cyclohexyl "base pairs" stabilize duplexes and intensify pyrene fluorescence by shielding it from natural base pairs

Author keywords

[No Author keywords available]

Indexed keywords

BASE PAIRING; BASE PAIRS; CD SPECTRA; CYCLOHEXYL; DNA DUPLEXES; DUPLEX STABILITY; ELECTRON TRANSFER; FLUORESCENT LABELING AGENT; HELICAL STRUCTURES; HYDROPHOBIC INTERACTIONS; IMINO PROTONS; ISOPROPYL GROUPS; NATURAL BASE; NUCLEOBASES; PYRENE FLUORESCENCE; THERMO DYNAMIC ANALYSIS;

EID: 84857536060     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06325a     Document Type: Article
Times cited : (15)

References (46)
  • 42
    • 38849094607 scopus 로고    scopus 로고
    • This quantum yield is lower than pyrene-modified DNA in other reports. In this study, 1-pyrenebutyric acid unit was introduced into DNA through d-threoninol. Accordingly, pyrene is intercalated between base pairs and is highly quenched by nucleobases. See refs 35 and 38 We could not calculate the increasing rate of emission intensity of H2AP / H2B directly because the emission intensity of P1 / N was much lower than that of H2AP / H2B. The emission of P1 / H2B at high sensitivity was about 36 times higher than that of P1 / N. In addition, the emission intensity of H2AP / H2B at medium sensitivity was about 4.5 times higher than that of P1 / H2B. See Fig. S3 in the Supporting Information for actual data
    • J. N. Wilson Y. Cho S. Tan A. Cuppoletti E. T. Kool ChemBioChem 2008 9 279 285
    • (2008) ChemBioChem , vol.9 , pp. 279-285
    • Wilson, J.N.1    Cho, Y.2    Tan, S.3    Cuppoletti, A.4    Kool, E.T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.