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用于检测微阵列上生物分子相互作用的角度扫描表面等离子体共振成像

Angle-scanning SPR imaging for detection of biomolecular interactions on microarrays.

作者信息

Beusink J Bianca, Lokate Angelique M C, Besselink Geert A J, Pruijn Ger J M, Schasfoort Richard B M

机构信息

BIOS, Lab-on-a-Chip Group, MESA+ Research Institute, University of Twente, P.O. Box 217, 7500 AE Enschede, The Netherlands.

出版信息

Biosens Bioelectron. 2008 Jan 18;23(6):839-44. doi: 10.1016/j.bios.2007.08.025. Epub 2007 Sep 11.

Abstract

In this paper we describe the use of a commercial surface plasmon resonance (SPR) imaging instrument for monitoring the binding of biomolecules on user-defined regions of interest of a microarray. By monitoring the angle shift of the SPR-dip using a continuous angle-scanning mode instead of monitoring the change in reflectivity at a fixed angle, a linear relationship with respect to the mass density change on the surface will remain over a wide dynamic angle range of 8 degrees. Peptides (2.4 kDa) and proteins (150 kDa) were both spotted on the same sensor chip to illustrate that both, low and high molecular weight ligands with initial large differences in off-set SPR angles, can be applied within the same experiment. By using a fluorescently labeled antibody, SPR results can be confirmed by means of fluorescence microscopy after completion of a SPR experiment. SPR imaging in angle-scanning operation provides sensitive, accurate, and label-free detection of analyte binding on microarrays containing different molecular weight ligands.

摘要

在本文中,我们描述了使用商用表面等离子体共振(SPR)成像仪器来监测生物分子在微阵列用户定义的感兴趣区域上的结合情况。通过使用连续角度扫描模式监测SPR凹陷的角度偏移,而不是在固定角度监测反射率的变化,在8度的宽动态角度范围内,表面质量密度变化将保持线性关系。将肽(2.4 kDa)和蛋白质(150 kDa)都点样在同一传感器芯片上,以说明在同一实验中,初始SPR角度偏移差异很大的低分子量和高分子量配体都可以应用。通过使用荧光标记抗体,在SPR实验完成后,可以通过荧光显微镜确认SPR结果。角度扫描操作中的SPR成像为含有不同分子量配体的微阵列上分析物的结合提供了灵敏、准确且无标记的检测。

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