Department of Materials, Department of Bioengineering, and Institute for Biomedical Engineering, Imperial College London , Exhibition Road, London SW7 2AZ, United Kingdom.
Anal Chem. 2014 Jul 1;86(13):6410-7. doi: 10.1021/ac500777r. Epub 2014 Jun 10.
The development of novel assays for protease sensing plays an important role in clinical diagnostics and therapeutics. Herein, we report a supramolecular platform for label-free protease detection, based on protein/dye self-assembly and enzyme-triggered disassembly. In a typical case, coassembly of protamine sulfate and perylene dye via electrostatic attractions and π-π interactions caused significant colorimetric and fluorescent responses. Subsequent addition of trypsin was found to cleave the amide bonds of protein, triggering the dissociation of protein/dye aggregates and the release of perylene dyes. The enzyme-triggered disassembly was transduced into multiple readouts including absorption, fluorescence, and polarization, which were exploited for trypsin detection and inhibitor testing. This assay was also used for turn-on fluorescence detection of cathepsin B, an enzyme known to be overexpressed in mammalian cancer cells. The integration of supramolecular self-assembly into enzyme detection in this work has provided a novel label-free biosensing platform which is highly sensitive with multimodal readouts. The relative simplicity of the approach avoids the need for time-consuming substrate synthesis, and is also amenable to naked eye detection.
新型蛋白酶检测分析方法的发展在临床诊断和治疗中起着重要作用。在此,我们报告了一种基于蛋白质/染料自组装和酶触发解组装的无标记蛋白酶检测的超分子平台。在典型情况下,通过静电吸引和π-π相互作用将硫酸鱼精蛋白和苝染料共组装会引起明显的比色和荧光响应。随后加入胰蛋白酶被发现可以切割蛋白质的酰胺键,触发蛋白质/染料聚集体的解离和苝染料的释放。酶触发的解组装被转化为多种读出信号,包括吸收、荧光和偏振,可用于胰蛋白酶检测和抑制剂测试。该测定法还用于检测组织蛋白酶 B 的荧光开启,组织蛋白酶 B 是一种已知在哺乳动物癌细胞中过度表达的酶。本工作将超分子自组装与酶检测相结合,提供了一种具有高灵敏度和多模态读出信号的新型无标记生物传感平台。该方法相对简单,避免了耗时的底物合成,并且也适用于肉眼检测。