[一种新的SELEX方法筛选HIV-1 P24抗原]。

中华实验和临床病毒学杂志 Pub Date : 2013-06-01
Shao-Bing Zhan, Xiao-Guang Zhang, Hong-Xia Li, Yi Zeng
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引用次数: 0

摘要

目的:筛选能与P24抗原紧密特异性结合的适配体,并验证其特异性和亲和力。方法:聚碳酸酯PCR板包被P24抗原,采用SELEX技术筛选PCR板上的适体。用软件分析了这些适体的一级和二级结构。通过HRP标记的链亲和素和生物素标记的适配体,通过ELISA验证了获得的适配体的亲和力和特异性。结果:聚碳酸酯PCR板可包被P24抗原。电泳分析显示适配体已富集。序列比对分析表明,这些适体序列一致,空间结构多样;酶联免疫吸附试验证实,适体与P24抗原具有较高的亲和力。结论:建立了一种筛选能特异性、紧密结合HIV-1 P24抗原的适体的简便方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A novel SELEX method for screening of HIV-1 P24 antigen].

Objective: To screen aptamers that can bind P24 antigen tightly and specificly, and verify its specificity and affinity.

Methods: Polycarbonate PCR plate was coated with P24 antigen and SELEX technology was used to screen aptamer on the PCR plate. The primary and secondary structure of these aptamers was analyzed by software. Through HRP labeled streptavidin and biotin labeled aptamers, the affinity and specificity of obtained aptamers were verified by ELISA.

Results: The polycarbonate PCR plate could be coated with P24 antigen. Electrophoretic analysis showed the aptamers had been enriched. Sequence aligment analysis showed that these aptamers have consensus sequence and their apatial structure was multiple; ELISA verified that aptamers had high affinity with P24 antigen.

Conclusion: A simple method was established for screening aptamers that can bind HIV-1 P24 antigen specificly and tightly.

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