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PVBLG150-8 is a synthetic, cationic helical polypeptide designed for the efficient delivery of nucleic acids, such as siRNA and plasmid DNA, into target cells. It is a derivative of poly(gamma-benzyl-L-glutamate) (PVBLG) with a degree of polymerization of approximately 150, where the benzyl side chains are modified with 1-(2-aminoethyl)piperidine (designated as amine '8' in screening libraries). Unlike traditional cationic polymers that often lose their secondary structure upon interaction with membranes or changes in pH, PVBLG150-8 maintains a stable alpha-helical conformation. This structural rigidity allows the polypeptide to penetrate cellular membranes directly and promote endosomal escape of the genetic cargo via a membrane-disruptive mechanism. Developed primarily in the laboratory of Jianjun Cheng at the University of Illinois, PVBLG150-8 has shown significant promise in preclinical cancer models for the systemic delivery of therapeutic genes, demonstrating high transfection efficiency and relatively low cytotoxicity compared to conventional vectors like polyethylenimine (PEI).
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