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Considering the low yield of expressed protein with pAcF incorporated, we engineered pCNFRS to improve the incorporation of pAcF by introducing a quadruple mutation H283T/P284S/M285D/D286V (TSDV) located at the anticodon recognition domain that was proved useful in pAzFRS for improving the incorporation of (p-azido-phenylalanine) pAzF 28

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These features allow them to: (i) passively diffuse between corneocytes (skin cells) due to their small size, (ii) enhance permeation through controlled modifications of surface properties, and (iii) target specific receptors on skin cells using ligands, ultimately leading to deeper delivery of the encapsulated drug

Although reactive electrophiles such as chloroacetamides are generally considered to be promiscuous in target binding, we demonstrated here using a BODIPY-labelled analogue that the chloroacetamide-based GSTO1 inhibitor C1-27 exhibited a low degree of nonspecific reactivity