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一种新型基于富勒烯的荧光探针用于胰蛋白酶。

A new specific fullerene-based fluorescent probe for trypsin.

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Engineering Research Center of Pesticide and Medicine Intermediate Clean Production, Ministry of Education, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan, 250014, PR China.

出版信息

Analyst. 2011 Mar 21;136(6):1199-203. doi: 10.1039/c0an00576b. Epub 2011 Jan 6.

Abstract

A novel fluorescent probe (C(60)-FL) was designed and synthesized for the direct determination of trypsin, based on photo-induced electron transfer (PET). The probe consists of two functional moieties: fluorescein which performs as a fluorophore and an electron donor, and fullerene (C(60)) which acts as an electron acceptor and trypsin substrate analogue. In the presence of trypsin, the probe exhibited fluorescence increase due to the inhibition of electron transfer by the combination of C(60)-FL with trypsin. The response of the probe to trypsin was direct and rapid. Experimental results showed that the increase in fluorescence intensity is proportional to the concentration of trypsin within the range of 4.40×10(-7) to 7.04×10(-5) g mL(-1) under the optimized experimental conditions. The detection limit of the proposed method was 40 ng mL(-1). The method had high selectivity for trypsin over other enzymes and proteins, such as lipase, α-amylase, bovine serum albumin, zinc metallothionein, glutathione reductase, thioredoxin and α-chymotrypsin etc. The remarkable properties of C(60)-FL help to extend the development of fluorescent probes for investigating enzymes in a biological context.

摘要

一种新型荧光探针(C(60)-FL)被设计并合成用于直接测定胰蛋白酶,基于光诱导电子转移(PET)。探针由两个功能部分组成:荧光素,作为荧光团和电子供体,和富勒烯(C(60)),作为电子受体和胰蛋白酶底物类似物。在存在胰蛋白酶的情况下,由于 C(60)-FL 与胰蛋白酶结合抑制电子转移,探针表现出荧光增强。探针对胰蛋白酶的响应是直接和快速的。实验结果表明,在优化的实验条件下,荧光强度的增加与胰蛋白酶的浓度在 4.40×10(-7) 至 7.04×10(-5) g mL(-1) 范围内成正比。该方法的检测限为 40 ng mL(-1)。与其他酶和蛋白质(如脂肪酶、α-淀粉酶、牛血清白蛋白、锌金属硫蛋白、谷胱甘肽还原酶、硫氧还蛋白和α-糜蛋白酶等)相比,该方法对胰蛋白酶具有高选择性。C(60)-FL 的显著性质有助于扩展荧光探针在生物环境中研究酶的发展。

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