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使用单分子敏感微阵列对蛋白质拷贝数进行绝对定量。

Absolute quantification of protein copy number using a single-molecule-sensitive microarray.

作者信息

Burgin Edward, Salehi-Reyhani Ali, Barclay Michael, Brown Aidan, Kaplinsky Joseph, Novakova Miroslava, Neil Mark A A, Ces Oscar, Willison Keith R, Klug David R

机构信息

Single Cell Proteomics Project, Institute of Chemical Biology, Imperial College London, London, SW7 2AZ, UK.

出版信息

Analyst. 2014 Jul 7;139(13):3235-44. doi: 10.1039/c4an00091a.

Abstract

We report the use of a microfluidic microarray incorporating single molecule detection for the absolute quantification of protein copy number in solution. In this paper we demonstrate protocols which enable calibration free detection for two protein detection assays. An EGFP protein assay has a limit of detection of <30 EGFP proteins in a microfluidic analysis chamber (limited by non-specific background binding), with a measured limit of linearity of approximately 6 × 10(6) molecules of analyte in the analysis chamber and a dynamic range of >5 orders of magnitude in protein concentration. An antibody sandwich assay was used to detect unlabelled human tumour suppressor protein p53 with a limit of detection of approximately 21 p53 proteins and a dynamic range of >3 orders of magnitude. We show that these protocols can be used to calibrate data retrospectively to determine the absolute protein copy number at the single cell level in two human cancer cell lines.

摘要

我们报告了一种结合单分子检测的微流控微阵列的应用,用于溶液中蛋白质拷贝数的绝对定量。在本文中,我们展示了可用于两种蛋白质检测分析的免校准检测方案。一种增强型绿色荧光蛋白(EGFP)检测分析在微流控分析腔中的检测限小于30个EGFP蛋白(受非特异性背景结合限制),分析腔中分析物的测量线性限约为6×10⁶个分子,蛋白质浓度动态范围大于5个数量级。采用抗体夹心分析检测未标记的人类肿瘤抑制蛋白p53,检测限约为21个p53蛋白,动态范围大于3个数量级。我们表明,这些方案可用于回顾性校准数据,以确定两种人类癌细胞系单细胞水平的绝对蛋白质拷贝数。

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