Continuous protease assays using liquid crystal as a reporter

Abstract

Abnormal protease activities are associated with cancers, vascular diseases and Alzheimer diseases. Therefore, detection of protease activities has become increasingly important in recent years. Herein, we report a semi-quantitative, liquid crystal (LC)-based protease assay for naked-eye detection of protease activity. In this assay, casein molecules are cleaved by proteases into small peptide fragments, which can be quantified either by using Lowry’s method or using LC. In the latter, peptide fragments adsorb on a solid surface and disrupt LC to produce a bright spot for naked-eye detection. The bright spot is observed only when the surface-adsorbed peptide density exceeds a critical value. In the assay, a major challenge is how to separate undigested casein and remaining protease from peptide fragments to prevent their interferences with LC. To overcome this issue, trichloroacetic acid (TCA) is added to precipitate casein and proteases. By using the assay, we are able to detect 10 ng/mL of protease (activity 7.23 U/mg protease, R2 = 0.991) or 6.5 μg/mL of peptide fragments. Finally, a continuous protease assay is developed to minimize manual sampling and reduce errors in kinetic studies.