Liu Cui, Zhou Zhen, Zou Linling, Cao Yuan-Cheng, Liu Jun'An, Lin Yongjun
Key Laboratory of Optoelectronic Chemical Materials and Devices, Ministry of Education, School of Chemical and Environmental Engineering, Jianghan University, Wuhan, 430056, China.
College of Science, Huazhong Agricultural University, Wuhan, China.
J Fluoresc. 2016 Mar;26(2):451-7. doi: 10.1007/s10895-015-1731-x. Epub 2015 Dec 7.
A highly sensitive transgenic protein analysis method was proposed here based on fluorescein diacetate (FDA). First, FDA was prepared by the ball mill to harvest the nano-sized organic particles. Further examines showed that the FDA size can be controlled by the speed of centrifugation which can obtain FDA in well-distributed size. Cy3 antibody immobilization tests showed that the proteins can attach onto the FDA particles while keep bioactivities. FDA and Cry1Ac antibody immunoassay tests showed that when the FDA particle was in 150 nm, the linear range was 0.01 ng/L-30 μg/mL. And it has the lower detection limitation of 0.01 ng/L, which is 100 times more sensitive than the ELISA methods. These results indicate that the FDA related immunoassays are the promising approach in the transgenic analysis.
本文提出了一种基于荧光素二乙酸酯(FDA)的高灵敏度转基因蛋白分析方法。首先,通过球磨制备FDA以收获纳米级有机颗粒。进一步研究表明,FDA的尺寸可通过离心速度控制,从而获得尺寸分布均匀的FDA。Cy3抗体固定化试验表明,蛋白质可附着在FDA颗粒上并保持生物活性。FDA与Cry1Ac抗体免疫分析试验表明,当FDA颗粒尺寸为150 nm时,线性范围为0.01 ng/L至30 μg/mL。其检测下限为0.01 ng/L,比酶联免疫吸附测定(ELISA)方法灵敏100倍。这些结果表明,与FDA相关的免疫分析是转基因分析中一种很有前景的方法。