将表面等离子体共振 (SPR) 应用于多种蛋白质-配体相互作用的研究。

Dana M. Burris, Samuel W. Gillespie, Emma Joy Campbell, S. Nick Ice, Vikas Yadav, William D. Picking, Christian L. Lorson, Kamal Singh
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引用次数: 0

摘要

酶/蛋白质的功能表征需要确定小分子或其他生物大分子与目标蛋白质的结合亲和力。现有的几种技术,如蛋白质组学和药物发现策略,都需要精确、高通量的检测方法,以快速、可靠地筛选出潜在的候选药物,供进一步测试。表面等离子体共振(SPR)是一种成熟的无标记技术,可直接测量生物分子的亲和力。SPR 检测需要将一种相互作用成分(配体)固定在导电金属(主要是金或银)上,并使含有潜在结合伙伴(分析物)的溶液持续流过表面。当偏振光激发金属和介电介质界面上的电子,产生平行于表面传播的电磁波时,就会产生 SPR 现象。配体和分析物之间相互作用引起的折射率变化可通过检测反射光来测量,从而提供有关动力学和特异性的实时数据。SPR 的一个主要用途是识别粗植物提取物中与特定分子结合的化合物。SPR 成像和局部 SPR(LSPR)是用于植物或哺乳动物病原体原位检测和药物发现研究的更便宜、更便携的替代方法。在活体植物研究中,LSPR 尤其具有直接附着于测试组织的优势。在此,我们介绍了利用基于 SPR 的检测方法精确分析蛋白质配体相互作用的三种方案。© 2024 Wiley Periodicals LLC.基本方案 1:病毒逆转录酶多态性结合亲和力的 SPR 比较 基本方案 2:粗植物提取物蛋白质结合剂的 SPR 筛选 基本方案 3:使用抗体结合的金纳米粒子进行基于 SPR 的局部抗原检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Applications of Surface Plasmon Resonance (SPR) to the Study of Diverse Protein-Ligand Interactions

Functional characterization of enzymes/proteins requires determination of the binding affinity of small molecules or other biomolecules with the target proteins. Several available techniques, such as proteomics and drug discovery strategies, require a precise and high-throughput assay for rapid and reliable screening of potential candidates for further testing. Surface plasmon resonance (SPR), a well-established label-free technique, directly measures biomolecular affinities. SPR assays require immobilization of one interacting component (ligand) on a conductive metal (mostly gold or silver) and a continuous flow of solution containing potential binding partner (analyte) across the surface. The SPR phenomenon occurs when polarized light excites the electrons at the interface of the metal and the dielectric medium to generate electromagnetic waves that propagate parallel to the surface. Changes in the refractive index due to interaction between the ligand and analyte are measured by detecting the reflected light, providing real-time data on kinetics and specificity. A prominent use of SPR is identifying compounds in crude plant extracts that bind to specific molecules. Procedures that utilize SPR are becoming increasingly applicable outside the laboratory setting, and SPR imaging and localized SPR (LSPR) are cheaper and more portable alternative for in situ detection of plant or mammalian pathogens and drug discovery studies. LSPR, in particular, has the advantage of direct attachment to test tissues in live-plant studies. Here, we describe three protocols utilizing SPR-based assays for precise analysis of protein-ligand interactions. © 2024 Wiley Periodicals LLC.

Basic Protocol 1: SPR comparison of binding affinities of viral reverse transcriptase polymorphisms

Basic Protocol 2: SPR screening of crude plant extract for protein-binding agents

Basic Protocol 3: Localized SPR–based antigen detection using antibody-conjugated gold nanoparticles

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