Proteostasis is an important biological event that regulates protein synthesis, folding and degradation1. We previously reported that an aggregation-induced emission (AIE) luminogen, TPE-MI2, which can be used as a great tool to quantify proteostasis imbalance by luminescence upon conjugation with exposed cysteine thiols. Upon structural optimization, we have created a series of TPE-MI analogues with better spectral properties while remaining minimal cytotoxicity, compared to TPE-MI. In this poster, I will present the applications of these probes for reporting on proteostatic stress in cells.