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Versatile targeting system for lentiviral vectors involving biotinylated targeting molecules.
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- Additional Information
- Source:
Publisher: Academic Press Country of Publication: United States NLM ID: 0110674 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-0341 (Electronic) Linking ISSN: 00426822 NLM ISO Abbreviation: Virology Subsets: MEDLINE
- Publication Information:
Original Publication: New York, Academic Press.
- Subject Terms:
- Abstract:
Conjugating certain types of lentiviral vectors with targeting ligands can redirect the vectors to specifically transduce desired cell types. However, extensive genetic and/or biochemical manipulations are required for conjugation, which hinders applications for targeting lentiviral vectors for broader research fields. We developed envelope proteins fused with biotin-binding molecules to conjugate the pseudotyped vectors with biotinylated targeting molecules by simply mixing them. The envelope proteins fused with the monomeric, but not tetrameric, biotin-binding molecules can pseudotype lentiviral vectors and be conjugated with biotinylated targeting ligands. The conjugation is stable enough to redirect lentiviral transduction in the presence of serum, indicating their potential in in vivo . When a signaling molecule is conjugated with the vector, the conjugation facilitates transduction and signaling in a receptor-specific manner. This simple method of ligand conjugation and ease of obtaining various types of biotinylated ligands will make targeted lentiviral transduction easily applicable to broad fields of research.
(Copyright © 2018 Elsevier Inc. All rights reserved.)
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- Grant Information:
DP5 OD019815 United States OD NIH HHS; R01 AI108400 United States AI NIAID NIH HHS; R21 AI095004 United States AI NIAID NIH HHS
- Contributed Indexing:
Keywords: Biotin; Lentiviral vectors; Rhizavidin; Signaling; Streptavidin; Targeting
- Accession Number:
0 (Viral Envelope Proteins)
6SO6U10H04 (Biotin)
- Publication Date:
Date Created: 20181006 Date Completed: 20190107 Latest Revision: 20191201
- Publication Date:
20240829
- Accession Number:
PMC6269213
- Accession Number:
10.1016/j.virol.2018.09.017
- Accession Number:
30290312
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