Chen Huan, Zheng Yue, Jiang Jian-Hui, Wu Hai-Long, Shen Guo-Li, Yu Ru-Qin
State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.
Biosens Bioelectron. 2008 Dec 1;24(4):684-9. doi: 10.1016/j.bios.2008.06.031. Epub 2008 Jul 1.
A novel chemiluminescence biosensor based on a supported lipid layer incorporated with ganglioside GM1 was developed for the detection of cholera toxin. The planar supported lipid membrane was prepared as biosensing interface via spontaneous spread of ganglioside-incorporated phospholipid vesicles on the octadecanethiol-coated gold surface. The specific interaction of multivalent CT by ganglioside GM1 molecules enables the biosensor to be implemented via a sandwiched format using a liposome probe functionalized with GM1 and horseradish peroxidase (HRP). Then, the presence of the target CT could be determined via the HRP-catalyzed enhanced chemiluminescence reaction. The developed strategy offers several unique advantages over conventional biosensors in that it allows for an easy construction and renewal of the sensing interface, a small background signal due to low non-specific adsorption of serum constituents on the lipid membrane, and effective immobilization of multiple biocatalytic amplifiers and recognition components via common phospholipid reagents. The developed biosensor was shown to give chemiluminescence signal in linear correlation to CT concentration within the range from 1pgmL(-1) to 1ngmL(-1) with readily achievable detection limit of 0.8pgmL(-1).
一种基于掺入神经节苷脂GM1的支撑脂质层的新型化学发光生物传感器被开发用于霍乱毒素的检测。通过将掺入神经节苷脂的磷脂囊泡在十八烷硫醇包被的金表面上自发铺展,制备平面支撑脂质膜作为生物传感界面。神经节苷脂GM1分子与多价霍乱毒素的特异性相互作用使得该生物传感器能够通过夹心形式实现,使用用GM1和辣根过氧化物酶(HRP)功能化的脂质体探针。然后,通过HRP催化的增强化学发光反应可以确定目标霍乱毒素的存在。与传统生物传感器相比,所开发的策略具有几个独特的优势,即它允许传感界面的轻松构建和更新,由于血清成分在脂质膜上的非特异性吸附低而背景信号小,以及通过常见的磷脂试剂有效固定多种生物催化放大器和识别组件。所开发的生物传感器在1pgmL(-1)至1ngmL(-1)范围内显示出与霍乱毒素浓度呈线性相关的化学发光信号,检测限易于达到0.8pgmL(-1)。