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Label-free fluorescent probing of G-quadruplex formation and real-time monitoring of DNA folding by a quaternized tetraphenylethene salt with aggregation-induced emission characteristics.
Hong, Yuning; Häussler, Matthias; Lam, Jacky W Y; Li, Zhen; Sin, King Keung; Dong, Yongqiang; Tong, Hui; Liu, Jianzhao; Qin, Anjun; Renneberg, Reinhard; Tang, Ben Zhong.
Afiliación
  • Hong Y; Department of Chemistry, The Hong Kong University of Science & Technology, Clear Water Bay, Kowloon, Hong Kong, China.
Chemistry ; 14(21): 6428-37, 2008.
Article en En | MEDLINE | ID: mdl-18512826
Biosensing processes such as molecular beacons require non-trivial effort to covalently label or mark biomolecules. We report here a label-free DNA assay system with a simple dye with aggregation-induced emission (AIE) characteristics as the fluorescent bioprobe. 1,1,2,2-Tetrakis[4-(2-bromoethoxy)phenyl]ethene is nonemissive in solution but becomes highly emissive when aggregated. This AIE effect is caused by restriction of intramolecular rotation, as verified by a large increase in the emission intensity by increasing viscosity and decreasing temperature of the aqueous buffer solution of 1,1,2,2-tetrakis[4-(2-triethylammonioethoxy)phenyl]ethene tetrabromide (TTAPE). When TTAPE is bound to a guanine-rich DNA strand (G1) via electrostatic attraction, its intramolecular rotation is restricted and its emission is turned on. When a competitive cation is added to the G1 solution, TTAPE is detached and its emission is turned off. TTAPE works as a sensitive poststaining agent for poly(acrylamide) gel electrophoresis (PAGE) visualization of G1. The dye is highly affinitive to a secondary structure of G1 called the G-quadruplex. The bathochromic shift involved in the G1 folding process allows spectral discrimination of the G-quadruplex from other DNA structures. The strong affinity of TTAPE dye to the G-quadruplex structure is associated with a geometric fit aided by the electrostatic attraction. The distinct AIE feature of TTAPE enables real-time monitoring of folding process of G1 in the absence of any pre-attached fluorogenic labels on the DNA strand. TTAPE can be used as a K+ ion biosensor because of its specificity to K+-induced and -stabilized quadruplex structure.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estilbenos / ADN / G-Cuádruplex / Colorantes Fluorescentes / Compuestos de Amonio Cuaternario Límite: Humans Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2008 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estilbenos / ADN / G-Cuádruplex / Colorantes Fluorescentes / Compuestos de Amonio Cuaternario Límite: Humans Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2008 Tipo del documento: Article País de afiliación: China Pais de publicación: Alemania