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基于单纳米颗粒追踪的膜受体-配体相互作用检测

Single nanoparticle tracking-based detection of membrane receptor-ligand interactions.

作者信息

Yang Yun-Hee, Nam Jwa-Min

机构信息

Department of Chemistry, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul, 151-747, South Korea.

出版信息

Anal Chem. 2009 Apr 1;81(7):2564-8. doi: 10.1021/ac802477h.

Abstract

We developed a single nanoparticle tracking-based detection method for membrane-associated molecules using a paucivalent gold nanoparticle (AuNP)-modified supported lipid bilayer (SLB) platform. Here, the binding activity of membrane-associated molecules (cholera toxin binding to ganglioside GM(1) in this case) was determined by calculating the diffusion coefficients of membrane-tethered AuNPs. This nonbleaching nanoparticle-based method provides >100-fold improvement in sensitivity for the same target without optimization over the fluorophore-based method that also has photobleaching and photoblinking problems. This new detection platform and analysis method could be used for membrane-associated molecule biosensor and screening assay development.

摘要

我们开发了一种基于单个纳米颗粒追踪的膜相关分子检测方法,该方法使用了多价金纳米颗粒(AuNP)修饰的支撑脂质双层(SLB)平台。在此,膜相关分子(在这种情况下为霍乱毒素与神经节苷脂GM(1)的结合)的结合活性通过计算膜 tethered AuNPs 的扩散系数来确定。这种基于非漂白纳米颗粒的方法在不进行优化的情况下,对于相同目标的灵敏度比基于荧光团的方法提高了100倍以上,而基于荧光团的方法还存在光漂白和光闪烁问题。这种新的检测平台和分析方法可用于膜相关分子生物传感器和筛选分析的开发。

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