National University of Singapore, 4 Engineering Drive 4, Singapore 117585.
Analyst. 2017 May 30;142(11):1867-1881. doi: 10.1039/c6an02647h.
Proteases play a pivotal role in regulating important physiological processes from food digestion to blood clotting. They are also important biomarkers for many diseases such as cancers. The importance of proteases has led to extensive efforts in the screening of proteases and their inhibitors as potential drug molecules. For example, human immunodeficiency virus (HIV) patients have been treated with HIV-1 protease inhibitors to prolong the life expectancy of patients. Such a close relationship between diseases and proteases provides a strong motivation for developing sensitive, selective, and robust protease assays and sensors, which can be exploited to discover new proteases and inhibitors. In this aspect, protease assays based on levels of proteolytic activities are more relevant than protease affinity assays such as immunoassays. In this review, recent developments of protease activity assays based on different detection principles are discussed and compared. For homogenous assays, fluorescence-based techniques are the most popular due to their high sensitivity and quantitative results. However, homogeneous assays have limited multiplex sensing capabilities. In contrast, heterogeneous assays can be employed to detect multiple proteases simultaneously, given the microarray technology that is already available. Among them, electrochemical methods, surface spectroscopy techniques, and enzyme-linked peptide protease assays are commonly used. Finally, recent developments in liquid crystal (LC)-based protease assays and their applications for detecting proteases and their inhibitors are discussed.
蛋白酶在调节从食物消化到血液凝固等重要生理过程中起着关键作用。它们也是许多疾病(如癌症)的重要生物标志物。蛋白酶的重要性促使人们广泛筛选蛋白酶及其抑制剂作为潜在的药物分子。例如,人类免疫缺陷病毒(HIV)患者已接受 HIV-1 蛋白酶抑制剂治疗,以延长患者的预期寿命。疾病与蛋白酶之间的这种密切关系为开发敏感、选择性和稳健的蛋白酶检测和传感器提供了强大的动力,这些传感器可用于发现新的蛋白酶和抑制剂。在这方面,基于蛋白水解活性水平的蛋白酶检测比基于亲和力的蛋白酶检测(如免疫测定)更相关。在这篇综述中,讨论并比较了基于不同检测原理的蛋白酶活性检测的最新进展。对于均相测定,基于荧光的技术由于其高灵敏度和定量结果而最受欢迎。然而,均相测定的多路复用传感能力有限。相比之下,由于已经存在的微阵列技术,可以用于同时检测多种蛋白酶的异相测定。其中,电化学方法、表面光谱技术和酶联肽蛋白酶测定法是常用的方法。最后,讨论了基于液晶(LC)的蛋白酶检测的最新进展及其在检测蛋白酶及其抑制剂方面的应用。