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芯片上抑制剂的对数标度剂量反应。

Log-scale dose response of inhibitors on a chip.

机构信息

Materials Research and Education Center, Department of Mechanical Engineering, Auburn University, Auburn, Alabama 36849, United States.

出版信息

Anal Chem. 2011 Aug 15;83(16):6148-53. doi: 10.1021/ac201177g. Epub 2011 Jul 19.

DOI:10.1021/ac201177g
PMID:21696192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3482625/
Abstract

We demonstrate the accommodation of log-scale concentration gradients of inhibitors on a single microfluidic chip with a semidirect dilution capability of reagents for the determination of the half-inhibitory concentration or IC(50). The chip provides a unique tool for hosting a wide-range of concentration gradient for studies that require an equal distribution of measuring points on a logarithmic scale. Using Matrix metalloproteinase IX and three of its inhibitors, marimastat, batimastat, and CP471474, we evaluated the IC(50) of each inhibitor with a single experiment. The present work could be applied to the systematic study of biochemical binding and inhibition processes particularly in the field of mechanistic enzymology and the pharmaceutical industry.

摘要

我们在单个微流控芯片上演示了抑制剂的对数浓度梯度的适应,该芯片具有半直接试剂稀释能力,用于测定半抑制浓度或 IC(50)。该芯片为 hosted 提供了一种独特的工具,用于在需要在对数尺度上均匀分布测量点的研究中,提供大范围的浓度梯度。我们使用基质金属蛋白酶 9 及其三种抑制剂,即 marimastat、batimastat 和 CP471474,在单个实验中评估了每种抑制剂的 IC(50)。本工作可应用于生化结合和抑制过程的系统研究,特别是在机制酶学和制药工业领域。

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本文引用的文献

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Creation of stepwise concentration gradient in picoliter droplets for parallel reactions of matrix metalloproteinase II and IX.在皮升级液滴中创建逐步浓度梯度,用于基质金属蛋白酶 II 和 IX 的平行反应。
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Determination of kinetic parameters, Km and kcat, with a single experiment on a chip.通过芯片上的单次实验测定动力学参数Km和kcat。
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Improvement of inner filter effect correction based on determination of effective geometric parameters using a conventional fluorimeter.基于使用传统荧光计测定有效几何参数来改进内滤光效应校正。
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A digital microfluidic approach to homogeneous enzyme assays.一种用于均相酶分析的数字微流控方法。
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