“…However, the techniques often required prelabeled molecular beacons or peptides, which can be time consuming, costly, and difficult to synthesize . To address this deficiency, researchers have developed several self-assembling methodologies by integrating different substrates with signal enhancing reported through noncovalent interactions, including a series of aggregation induced emission luminogens (AIEgens). , These strategies generally offer the additional advantages of a broad concentration range and a high signal-to-noise ratio. − However, these fluorescence-based methods rely on noncovalent interactions that can be affected by reaction medium, ionic strength, surface morphology, and protein foldedness so may introduce large variation among experiments and thus have a relatively low reliability. , Surprisingly, the use of covalent probes for the in situ formation of a sensing system for the detection of trypsin activity has not been reported.…”