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利用飞升级阵列和泊松统计对单个酶分子进行数字浓度读数

Digital concentration readout of single enzyme molecules using femtoliter arrays and Poisson statistics.

作者信息

Rissin David M, Walt David R

机构信息

Department of Chemistry, Tufts University, 62 Talbot Avenue, Medford, Massachusetts 02155, USA.

出版信息

Nano Lett. 2006 Mar;6(3):520-3. doi: 10.1021/nl060227d.

Abstract

Methods for accurately quantifying the concentration of a particular analyte in solution are all based on ensemble responses in which many analyte molecules give rise to the measured signal. In this paper, single molecules of beta-galactosidase were monitored using a 1 mm diameter fiber optic bundle with 2.4 x 10(5) individually sealed, femtoliter microwell reactors. By observation of the buildup of fluorescent products from single enzyme molecule catalysis over the array of reaction vessels and by application of a Poisson statistical analysis, a digital concentration readout was obtained. This approach should prove useful for single molecule enzymology and ultrasensitive bioassays. More generally, the ability to determine concentration by counting individual molecules offers a new approach to analysis of dilute solutions.

摘要

准确量化溶液中特定分析物浓度的方法均基于整体响应,即许多分析物分子产生测量信号。在本文中,使用直径为1毫米的光纤束监测β-半乳糖苷酶的单分子,该光纤束带有2.4×10⁵个单独密封的飞升级微孔反应器。通过观察单个酶分子在一系列反应容器中催化产生的荧光产物的积累,并应用泊松统计分析,获得了数字浓度读数。这种方法对于单分子酶学和超灵敏生物测定应该是有用的。更一般地说,通过对单个分子计数来确定浓度的能力为稀溶液分析提供了一种新方法。

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