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Lipid-peptide bioconjugation through pyridyl disulfide reaction chemistry and its application in cell targeting and drug delivery.

J Nanobiotechnology. 2019-06; 
de la Fuente-HerreruelaDiego,MonnappaAjay K,Muñoz-ÚbedaMónica,Morallón-PiñaAarón,EncisoEduardo,SánchezLuis,GiustiFabrice,NatalePaolo,López-MonteroI
Products/Services Used Details Operation
Peptide Synthesis Te peptides NH2-KRTGQYKLC-COOH and NH2- WEAA-LAEA-LAEA-LAE-H-LAEA-LAEA-LEALAACCOOH were synthesized by GenScript (Piscataway, NJ USA) and used without any further purifcation step. Get A Quote

摘要

The design of efficient drug delivery vectors requires versatile formulations able to simultaneously direct a multitude of molecular targets and to bypass the endosomal recycling pathway of cells. Liposomal-based vectors need the decoration of the lipid surface with specific peptides to fulfill the functional requirements. The unspecific binding of peptides to the lipid surface is often accompanied with uncontrolled formulations and thus preventing the molecular mechanisms of a successful therapy.

关键词

Disulfide bonds,Endosomal escape,GALA,Smart liposomes,Targeting pep