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一种用于流动注射免疫分析的可重复使用的特异性蛋白A包被的压电生物传感器。

A reusable and specific protein A-coated piezoelectric biosensor for flow injection immunoassay.

作者信息

Lu H C, Chen H M, Lin Y S, Lin J W

机构信息

Department of Chemical Engineering, Chang Gung University, Taoyuan, Taiwan 333, ROC.

出版信息

Biotechnol Prog. 2000 Jan-Feb;16(1):116-24. doi: 10.1021/bp9901320.

Abstract

A hydrophilic matrix of periodate-oxidized dextran was used as a double-sided linker to covalently immobilize Staphylococcus aureus protein A (SpA) molecules onto a poly-L-lysine-modified piezoelectric crystal surface to improve their stability, activity, and binding specificity with human immunoglobulin G (IgG) in flow injection assays. The prepared sensing crystals displayed best sensitivity and reusability at a flow rate of 140 microL/min. A human IgG concentration as low as 0.3 nM can be detected by this system. Up to 19 successive assay repetitions were achieved without significant loss of sensitivity using the same crystal. The analysis of adsorption kinetics indicates that such a preparation can greatly increase the amount of available active human IgG binding sites on immobilized SpA. Hardly any response arising from unspecific binding was detected. In addition, the sensing crystal prepared by this method was found to retain activity better than one prepared via direct deposition when stored in either wet or dry states. Finally, the prepared SpA-coated crystals were applied to the affinity immobilization of polyclonal goat anti-Schistosoma japonicum glutathione-S-transferase (GST) and were able to subsequently detect GST and its genetically engineered mutant either in a purified form or in the crude cell lysate.

摘要

以高碘酸盐氧化葡聚糖的亲水性基质作为双面连接体,将金黄色葡萄球菌蛋白A(SpA)分子共价固定在聚-L-赖氨酸修饰的压电晶体表面,以提高其在流动注射分析中与人类免疫球蛋白G(IgG)的稳定性、活性和结合特异性。制备的传感晶体在流速为140微升/分钟时显示出最佳的灵敏度和可重复使用性。该系统可检测低至0.3 nM的人类IgG浓度。使用同一晶体可实现多达19次连续测定重复,且灵敏度无明显损失。吸附动力学分析表明,这种制备方法可大大增加固定化SpA上可用的活性人类IgG结合位点数量。几乎未检测到非特异性结合产生的任何响应。此外,发现通过这种方法制备的传感晶体在湿态或干态储存时比通过直接沉积制备的晶体保留活性更好。最后,将制备的SpA包被晶体应用于山羊抗日本血吸虫谷胱甘肽-S-转移酶(GST)多克隆抗体的亲和固定,并能够随后检测纯化形式或粗细胞裂解物中的GST及其基因工程突变体。

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