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New Method Based on Capillary Electrophoresis with Laser-Induced Fluorescence Detection (CE-LIF) to Monitor Interaction between Nanoparticles and the Amyloid-beta Peptide

机译:基于毛细管电泳和激光诱导荧光检测(CE-LIF)的新方法,以监测纳米粒子与淀粉样β肽之间的相互作用。

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摘要

A novel application of capillary electrophoresis with laser-induced fluorescence detection (CE-LIF) was proposed to efficiently detect and monitor the interaction between polymeric nanoparticles and the beta-Amyloid peptide (A(beta)_(1-42)), a biomarker for Alzheimer's Disease (AD), at concentrations close to physiological conditions. The CE-LIF method allowed the interaction between PEGylated poly(alkyl cyanoacrylate) nanoparticles (NPs) and the soluble A(beta)_(1-42) peptide monomers to be highlighted. These results were confirmed by surface plasmon resonance (SPR) and confocal laser scanning microscopy (CLSM). Whereas SPR showed an interaction between the NPs and the A(beta)_(1-42) peptide, CLSM allowed the formation of large aggregates/assemblies at high NP and peptide concentrations to be visualized. All these results suggested that these nanoparticles could bind the A(beta)_(1-42) peptide and influence its aggregation kinetics. Interestingly, the non-PEGylated poly(alkyl cyanoacrylate) NPs did not alter the aggregation kinetics of the A(beta)_(1-42) peptide, thus emphasizing the high level of discrimination of the CELIF method with respect to NPs.
机译:提出了毛细管电泳在激光诱导荧光检测(CE-LIF)中的新应用,以有效检测和监测聚合物纳米颗粒与生物标志物β-淀粉样肽(Aβ_(1-42))之间的相互作用。用于阿尔茨海默氏病(AD),浓度接近生理条件。 CE-LIF方法使聚乙二醇化的聚(氰基丙烯酸烷基酯)纳米颗粒(NPs)和可溶性Aβ_(1-42)肽单体之间的相互作用得以突出显示。这些结果已通过表面等离子体激元共振(SPR)和共聚焦激光扫描显微镜(CLSM)证实。 SPR显示了NP与Aβ_(1-42)肽之间的相互作用,而CLSM允许在高NP和肽浓度下形成大的聚集体/装配体,并可以看到肽浓度。所有这些结果表明,这些纳米颗粒可以结合Aβ_(1-42)肽并影响其聚集动力学。有趣的是,非聚乙二醇化的聚(氰基丙烯酸烷基酯)NP没有改变Aβ_(1-42)肽的聚集动力学,因此强调了CELIF方法相对于NP的高区分度。

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