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基于表面等离子体荧光光谱的生物测定中的阿托摩尔灵敏度。

Attomolar sensitivity in bioassays based on surface plasmon fluorescence spectroscopy.

作者信息

Yu Fang, Persson Björn, Löfås Stefan, Knoll Wolfgang

机构信息

Max-Planck-Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.

出版信息

J Am Chem Soc. 2004 Jul 28;126(29):8902-3. doi: 10.1021/ja048583q.

Abstract

With the aid of a dextran matrix, the metal-induced fluorescence loss of bound fluorophores can be greatly reduced, and the distance dependence of the fluorescence yield could be largely convoluted. This is optimized for the limit of detection assessment of surface plasmon fluorescence spectroscopy. The model system was designed as a direct assay with mouse IgG covalently immobilized to the carboxymethyl dextran matrix of a CM5 sensor chip from Biacore. Time-resolved ultratrace detection of fluorophore (Alexa-Fluor 647)-labeled rabbit anti-mouse antibody down to 500 aM (10-18 M) was accomplished, corresponding to a binding rate of approximately 10 molecules mm-2 min-1.

摘要

借助葡聚糖基质,可大幅降低金属诱导的结合荧光团的荧光损失,并且荧光产率的距离依赖性也能在很大程度上被卷积。这针对表面等离子体荧光光谱的检测限评估进行了优化。该模型系统设计为一种直接测定法,将小鼠IgG共价固定到Biacore公司CM5传感器芯片的羧甲基葡聚糖基质上。实现了对荧光团(Alexa-Fluor 647)标记的兔抗小鼠抗体的时间分辨超痕量检测,检测下限低至500 aM(10⁻¹⁸ M),对应结合速率约为10个分子·mm⁻²·min⁻¹。

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