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大脑中剪切诱导的淀粉样蛋白形成:II. 监测淀粉样蛋白剪切过程及研究潜在腰椎穿刺问题的实验系统

Shear-Induced Amyloid Formation in the Brain: II. An Experimental System for Monitoring Amyloid Shear Processes and Investigating Potential Spinal Tap Problems.

作者信息

Trumbore Conrad N

机构信息

Department of Chemistry and Biochemistry, University of Delaware, Kennett Square, PA, USA.

出版信息

J Alzheimers Dis. 2017;59(2):543-557. doi: 10.3233/JAD-170259.

DOI:10.3233/JAD-170259
PMID:28671126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5523842/
Abstract

Liquid sheared amyloid-β (Aβ) initiates amyloid cascade reactions, producing unstable, potentially toxic oligomers. There is a need for new analytical tools with which to study these oligomers. A very small bore capillary flow system is proposed as a tool for studying the effects of liquid shear in amyloid research. This simple system consists of injecting a short cylindrical liquid sample plug containing dissolved amyloid into a liquid mobile phase flowing through an empty, very small internal diameter capillary tube. For liquid samples containing a single protein sample, under conditions in which there is laminar flow and limited sample protein molecular diffusion, chromatograms monitoring the optical protein absorbance of capillary effluent contain either one or two peaks, depending on the mobile phase flow rate. By controlling the sample diffusion times through changes in flow rate and/or capillary diameter, this tool can be used to generate aliquot samples with precise, reproducible amounts of shear for exploring the effects of variable shear on amyloid systems. The tool can be used for producing in-capillary stopped flow spectra of shear-stressed Aβ monomers as well as for kinetic studies of Aβ dimer- and oligomer-forming reactions between shear stressed Aβ monomers. Many other experiments are suggested using this experimental tool for studying the effects of shear on different Aβ and other amyloid systems, including testing for potentially serious amyloid sampling errors in spinal tap quantitative analysis. The technique has potential as both a laboratory research and a clinical tool.

摘要

液体剪切的淀粉样β蛋白(Aβ)引发淀粉样蛋白级联反应,产生不稳定的、可能有毒的寡聚体。需要新的分析工具来研究这些寡聚体。一种非常小内径的毛细管流动系统被提议作为研究淀粉样蛋白研究中液体剪切效应的工具。这个简单的系统包括将一个含有溶解淀粉样蛋白的短圆柱形液体样品塞注入到流经一个空的、内径非常小的毛细管的液体流动相中。对于含有单一蛋白质样品的液体样品,在层流且样品蛋白质分子扩散有限的条件下,监测毛细管流出物中蛋白质光学吸光度的色谱图根据流动相流速包含一个或两个峰。通过改变流速和/或毛细管直径来控制样品扩散时间,该工具可用于生成具有精确、可重复剪切量的等分试样,以探索可变剪切对淀粉样蛋白系统的影响。该工具可用于生成剪切应力作用下Aβ单体的毛细管内停流光谱,以及用于研究剪切应力作用下Aβ单体之间形成二聚体和寡聚体反应的动力学研究。还建议使用这个实验工具进行许多其他实验,以研究剪切对不同Aβ和其他淀粉样蛋白系统的影响,包括检测脊髓穿刺定量分析中潜在的严重淀粉样蛋白采样误差。该技术具有作为实验室研究工具和临床工具的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/c6050c53ba84/jad-59-jad170259-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/7acbd029a5b7/jad-59-jad170259-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/37fbfdaff150/jad-59-jad170259-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/c0722ebe8526/jad-59-jad170259-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/c6050c53ba84/jad-59-jad170259-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/7acbd029a5b7/jad-59-jad170259-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/37fbfdaff150/jad-59-jad170259-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/c0722ebe8526/jad-59-jad170259-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c30/5523842/c6050c53ba84/jad-59-jad170259-g004.jpg

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