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纳米阵列:一种进行酶促测定的方法。

Nanoarrays: a method for performing enzymatic assays.

作者信息

Dietrich Heidelinde R C, Knoll Johann, van den Doel Lennert R, van Dedem Gijs W K, Daran-Lapujade Pascale A S, van Vliet Lucas J, Moerman Rob, Pronk Jack T, Young Ian T

机构信息

Department of Imaging Science & Technology, Faculty of Applied Science, Delft University of Technology, Lorentzweg 1, 2628 CJ Delft, The Netherlands.

出版信息

Anal Chem. 2004 Jul 15;76(14):4112-7. doi: 10.1021/ac049737n.

Abstract

Conventional enzymatic assays for alcohol dehydrogenase, pyruvate kinase, and enolase performed in 96-well microtiter plates were compared with assays monitored in 25-well nanoarrays. All miniaturized reactions could be performed in maximum volumes of 6.3-8 nL and were read out with a conventional fluorescence microscope system equipped with a scientific grade CCD camera. Substrate and cofactor were already present inside the wells after having been presprayed, or they were applied in solution to the wells of the nanoarray shortly before the assays started. For all of the assays, commercially available enzymes and enzymes present in cell-free extracts were used. Assays carried out in premixed nanoarrays gave results comparable to those performed in presprayed nanoarrays. Enzyme activities determined in nanoarrays by using two different methods were in good agreement with assays performed in microtiter plates. Also, good correspondence was found between expected and observed enzyme levels. In short, enzymatic assays performed in premixed and in particular in presprayed nanoarrays are a promising low-volume and low-reagent- and sample-consuming alternative to current methodology and could find applications in many different areas of analytical chemistry.

摘要

将在96孔微量滴定板中进行的乙醇脱氢酶、丙酮酸激酶和烯醇化酶的传统酶促测定法与在25孔纳米阵列中监测的测定法进行了比较。所有微型反应的最大体积可为6.3 - 8纳升,并用配备科学级电荷耦合器件相机的传统荧光显微镜系统读取结果。底物和辅因子在预喷入孔内后就已存在,或者在测定开始前不久以溶液形式加入纳米阵列的孔中。对于所有测定,使用了市售酶和无细胞提取物中存在的酶。在预混合纳米阵列中进行的测定结果与在预喷纳米阵列中进行的测定结果相当。通过两种不同方法在纳米阵列中测定的酶活性与在微量滴定板中进行的测定结果高度一致。此外,预期酶水平与观察到的酶水平之间也有良好相关性。简而言之,在预混合尤其是预喷纳米阵列中进行的酶促测定是一种有前景的低体积、低试剂和低样品消耗的替代当前方法的方法,可在分析化学的许多不同领域找到应用。

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