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使用开放表面等离子体共振(OpenSPR)来表征蛋白质-蛋白质相互作用的结合亲和力。

Use of Open Surface Plasmon Resonance (OpenSPR) to Characterize the Binding Affinity of Protein-Protein Interactions.

作者信息

Zhu Cassie Shu, Li Jianhua, Wang Haichao

机构信息

The Feinstein Institutes for Medical Research, Northwell Health, 350 Community Drive, Manhasset, NY, USA.

Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, 500 Hofstra Blvd., Hempstead, NY, USA.

出版信息

Bio Protoc. 2023 Sep 5;13(17):e4795. doi: 10.21769/BioProtoc.4795.

Abstract

Surface Plasmon Resonance(SPR) is a label-free optical technique to assess protein-protein interaction kinetics and affinities in a real-time setting. Traditionally, Biacore SPR employs a continuous film of gold to detect any change in the angle of re-emitted light when the refractive index of a ligand conjugated to the flat gold surface is altered by its interaction with a local analyte. In contrast, the Nicoya Lifesciences' OpenSPR technology uses gold nanoparticles to detect small changes in the absorbance peak wavelength of a conjugated ligand after its engagement by an analyte. Specifically, when broadband white light is shone onto the gold nanoparticles, it produces a strong resonance absorbance peak corresponding to the refractive index of a ligand conjugated to the surface of gold nanoparticles. Upon its interaction with an analyte, however, the absorbance wavelength peak of the conjugated ligand will be changed and timely recorded as sensorgrams of dynamic ligand-analyte interactions. Thus, the improvement in the detection method (from traditional detection of changes in the angle of re-emitted light to the contemporary detection of changes in the wavelength of the absorbance peak) features OpenSPR as a cost-effective and user-friendly technique for in-depth characterization of protein-protein interactions. Here, we describe the detailed method that we used to characterize procathepsin L (pCTS-L) interactions with two putative pattern recognition receptors (TLR4 and RAGE) using the 1st generation of Nicoya Lifesciences' OpenSPR instrument with a 1-channel detection. Key features • Nicoya OpenSPR is a benchtop small-size equipment that provides in-depth label-free binding kinetics and affinity measurement for protein-protein interactions in real-time fashion. • This technology is relatively intuitive and user-friendly for scientists at any skill level. • OpenSPR sensors employ nanotechnology to reduce the cost of manufacturing complex optical hardware and Sensor Chips, and similarly reduce the consumption of precious analyte samples. • The manufacturer provides online training for OpenSPR (Catalog: TRAIN-REMOTE) and TraceDrawer (Catalog: TRAIN-TD) to customer scientists.

摘要

表面等离子体共振(SPR)是一种无需标记的光学技术,可在实时环境中评估蛋白质-蛋白质相互作用的动力学和亲和力。传统上,Biacore SPR使用连续的金膜来检测当与平坦金表面共轭的配体与局部分析物相互作用而导致其折射率改变时,重新发射光角度的任何变化。相比之下,Nicoya生命科学公司的OpenSPR技术使用金纳米颗粒来检测共轭配体在与分析物结合后其吸收峰波长的微小变化。具体而言,当宽带白光照射到金纳米颗粒上时,会产生一个与共轭到金纳米颗粒表面的配体折射率相对应的强共振吸收峰。然而,当它与分析物相互作用时,共轭配体的吸收波长峰会发生变化,并及时记录为动态配体-分析物相互作用的传感图。因此,检测方法的改进(从传统的检测重新发射光角度的变化到当代检测吸收峰波长的变化)使OpenSPR成为一种经济高效且用户友好的技术,可用于深入表征蛋白质-蛋白质相互作用。在此,我们描述了我们使用第一代Nicoya生命科学公司的具有单通道检测功能的OpenSPR仪器来表征组织蛋白酶L前体(pCTS-L)与两种假定的模式识别受体(TLR4和RAGE)相互作用的详细方法。关键特性 • Nicoya OpenSPR是一种台式小型设备,可实时为蛋白质-蛋白质相互作用提供深入的无标记结合动力学和亲和力测量。 • 该技术对于任何技能水平的科学家来说都相对直观且用户友好。 • OpenSPR传感器采用纳米技术来降低制造复杂光学硬件和传感器芯片的成本,同样也减少了珍贵分析物样品的消耗。 • 制造商为客户科学家提供OpenSPR(目录:TRAIN-REMOTE)和TraceDrawer(目录:TRAIN-TD)的在线培训。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9990/10502159/036f05de7525/BioProtoc-13-17-4795-g001.jpg

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