“…While an ester usually be hydrolyzed at basic pH and at elevated temperature, the catalytic triad of esterase performs similar reaction at neutral buffer solution (pH ~7.0) and at physiological temperature 24,25 . Researchers put considerable effort to design the synthetic mimic of esterase using de novo design 26,27 , dendrimer 28 , polymer 29 , membrane 30,31 , selfassembling peptides 32,33 , nanofibers 34 and amyloid fibrils 5,33,35 to cleave an ester at the physiological condition. However, most of the designs are only able to cleave the active ester like p-nitrophenol ester 5,27,[29][30][31][32][33][34][35][36] and remain ineffective towards normal non-activated esters 37 .…”