“…This FRET-based concept has been extensively used to construct molecular beacons for sensing of DNA, RNA, and other biomolecules. − Third, the tetrapeptide −GFLG–, a well-established cathepsin B (CatB) substrate, , was used as the cleavable linker to bridge the drug to the BHQ-2 quencher through a lysine junction, modulating the release of Dox while serving as a CatB sensor. Cathepsin B is a lysosomal protease known to be overexpressed in many types of cancer. − Finally, octa-arginine (R8), a well-studied cell penetrating peptide (CPP) sequence, was used to assist in the effective cellular internalization . All the molecules studied here were synthesized using a combined automatic and manual solid-phase peptide synthesis (SPPS) method as reported previously .…”