Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Red-shifted fluorescence from polyguanylic acid in aqueous solution at room temperature. / Kononov, A. I.; Bakulev, V. M.
в: Journal of Photochemistry and Photobiology B: Biology, Том 34, № 2-3, 01.01.1996, стр. 211-216.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Red-shifted fluorescence from polyguanylic acid in aqueous solution at room temperature
AU - Kononov, A. I.
AU - Bakulev, V. M.
PY - 1996/1/1
Y1 - 1996/1/1
N2 - The absorption, fluorescence emission, fluorescence excitation and fluorescence polarization spectra of polyriboguanylic acid (poly(G)) were studied in aqueous solution at room temperature. Greatly red-shifted fluorescence from poly(G) in water was attributed to a small amount of the bases protonated on the N(7) atom. This was supported by the following points: (1) the fluorescence emission spectrum of guanosine 5'-monophosphate in acid pH conditions was very close to that of poly(G) in water, and their fluorescence excitation spectra were coincident, and (2) the red-shifted fluorescence band disappeared on increasing pH with the addition of tris(hydroxymethyl) amino methane. The fluorescence titration curve exhibited a maximum at pH 4.8 that was assigned to the four-stranded form of poly(G), with part of the bases being protonated. The protonation degree was found to depend on the ionic strength of the solution.
AB - The absorption, fluorescence emission, fluorescence excitation and fluorescence polarization spectra of polyriboguanylic acid (poly(G)) were studied in aqueous solution at room temperature. Greatly red-shifted fluorescence from poly(G) in water was attributed to a small amount of the bases protonated on the N(7) atom. This was supported by the following points: (1) the fluorescence emission spectrum of guanosine 5'-monophosphate in acid pH conditions was very close to that of poly(G) in water, and their fluorescence excitation spectra were coincident, and (2) the red-shifted fluorescence band disappeared on increasing pH with the addition of tris(hydroxymethyl) amino methane. The fluorescence titration curve exhibited a maximum at pH 4.8 that was assigned to the four-stranded form of poly(G), with part of the bases being protonated. The protonation degree was found to depend on the ionic strength of the solution.
KW - Fluorescence
KW - Fluorescence excitation spectra
KW - Guanine cations
KW - Polyguanylic acid
KW - Protonation
UR - http://www.scopus.com/inward/record.url?scp=0030199469&partnerID=8YFLogxK
U2 - 10.1016/1011-1344(96)07288-0
DO - 10.1016/1011-1344(96)07288-0
M3 - Article
AN - SCOPUS:0030199469
VL - 34
SP - 211
EP - 216
JO - Journal of Photochemistry and Photobiology B: Biology
JF - Journal of Photochemistry and Photobiology B: Biology
SN - 1011-1344
IS - 2-3
ER -
ID: 39285701