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使用基于聚二乙炔的荧光芯片对水源性病原体微小隐孢子虫进行非标记检测。

Non-labeled detection of waterborne pathogen Cryptosporidium parvum using a polydiacetylene-based fluorescence chip.

作者信息

Park Cheon Kyo, Kang Chang Duk, Sim Sang Jun

机构信息

Department of Chemical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.

出版信息

Biotechnol J. 2008 May;3(5):687-93. doi: 10.1002/biot.200700246.

Abstract

A non-labeling fluorescence sensor system was developed using polydiacetylene (PDA) liposomes composed of 10,12-pentacosadiynoic acid (PCDA) and 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) at a 8:2 molar ratio. The PDA liposomes were immobilized onto an amine-coated glass surface using peptide bonding between the carboxyl group of the liposome and the amine group of the glass surface. The optimum ratio of the cross linker (NHS/EDC) to PDA liposome was determined to be 50% for strong immobilization of the liposomes. Residual carboxyl groups of the PDA liposomes were selectively biotinylated, followed by sequential binding of streptavidin and biotin-antibody (bioreceptor). Finally, the performance of the PDA liposome chip was tested for detecting Cryptosporidium parvum, and yielded a detection limit of 1 x 10(3) oocysts/mL. From these results, it is expected that the PDA liposome chip will have high application potential for the detection of waterborne pathogens including C. parvum.

摘要

使用由摩尔比为8:2的10,12-二十五碳二炔酸(PCDA)和1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱(DMPC)组成的聚二乙炔(PDA)脂质体开发了一种非标记荧光传感器系统。通过脂质体的羧基与玻璃表面的胺基之间的肽键合,将PDA脂质体固定在胺涂层的玻璃表面上。为了使脂质体牢固固定,确定交联剂(NHS/EDC)与PDA脂质体的最佳比例为50%。对PDA脂质体的残留羧基进行选择性生物素化,然后依次结合链霉亲和素和生物素抗体(生物受体)。最后,测试了PDA脂质体芯片检测微小隐孢子虫的性能,检测限为1×10³卵囊/mL。从这些结果来看,预计PDA脂质体芯片在检测包括微小隐孢子虫在内的水生病原体方面将具有很高的应用潜力。

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