| Literature DB >> 31482462 |
Pengfei Zhang1, Hu Chen1, Jingyi Liu1, Gang Liu2,3,4.
Abstract
A series of ligand-targeted nanosystems have been rapidly exploited to selectively deliver drug molecules to desired cell populations. The conjugation of protein ligands to the nanoparticle (NP) surface endows nanovehicles with active targeting properties. However, the nonspecific covalent coupling of protein ligands to nanocarriers may compromise the protein targeting due to the uncontrolled ligand orientation as well as the decline in ligand activity during linkage process. With this regard, biomimetic synthetic strategies are employed for the preparation of genetically engineered nanovesicles (GNV) from cellular plasma membrane with targeting moieties on the surface in a ligand-oriented manner. Herein, we introduce the biomimetic synthetic strategy and procedures for GNV preparation. This chapter may guide readers to design analogous NPs for cell-specific targeting by displaying particular protein probes (e.g., antibody, nanobody, and single-chain antibody) on the surface of GNVs.Entities:
Keywords: Cell membrane vesicles; Drug delivery; Genetically engineered vesicles; Ligand-targeted delivery; Nanovesicles
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Year: 2019 PMID: 31482462 DOI: 10.1007/978-1-4939-9769-5_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745