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低分子量分析物识别过程中的负表面等离子体共振信号

Negative SPR Signals during Low Molecular Weight Analyte Recognition.

作者信息

Bonnet H, Coche-Guérente L, Defrancq E, Spinelli N, Van der Heyden A, Dejeu J

机构信息

Université Grenoble Alpes, CNRS, DCM UMR-5250, F-38000 Grenoble, France.

出版信息

Anal Chem. 2021 Mar 2;93(8):4134-4140. doi: 10.1021/acs.analchem.1c00071. Epub 2021 Feb 12.

Abstract

Surface plasmon resonance (SPR) is a powerful technique for studying biomolecular interactions mainly due to its sensitivity and real-time and label free advantages. While SPR signals are usually positive, only a few studies have reported sensorgrams with negative signals. The aim of the present work is to investigate and to explain the observation of negative SPR signals with the hypothesis that it reflects major changes in ligand conformation resulting from target binding. We demonstrated that these negative unconventional signals were due to the negative complex (ligand/analyte) refractive index increment (RII) deviation from the sum of the RII of the individual entities which counterbalanced the theoretical increase of the signal triggered by the target recognition and the ligand folding. We also found that the conformation change of biomolecules can induce a negative or a positive complex RII deviation depending on its sequence and immobilization mode.

摘要

表面等离子体共振(SPR)是一种用于研究生物分子相互作用的强大技术,主要是因为它具有灵敏度高、实时和无需标记的优点。虽然SPR信号通常是正的,但只有少数研究报道过具有负信号的传感图。本研究的目的是调查并解释负SPR信号的观察结果,其假设是它反映了由于靶标结合导致的配体构象的重大变化。我们证明,这些负的非常规信号是由于负的复合物(配体/分析物)折射率增量(RII)偏离了各个实体的RII之和,这抵消了由靶标识别和配体折叠引发的信号的理论增加。我们还发现,生物分子的构象变化可根据其序列和固定模式诱导负的或正的复合物RII偏差。

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