RRC ID 86859
著者 Jargalsaikhan BE, Muto M, Ema M.
タイトル Optimized Lentiviral Vector Production Using Dual-Pseudotyping with VSV-G and Sendai Virus HN Glycoproteins for Enhanced Gene Delivery in Diverse Cell Types.
ジャーナル Methods Mol Biol
Abstract Highly efficient gene delivery using lentiviral vectors is beneficial not only for basic cell science research but also for human gene therapy applications. Lentiviral pseudotyping with vesicular stomatitis virus G (VSV-G) is a commonly used method that enables the transduction of various cell types. However, the low expression of low-density lipoprotein-receptor, the primary receptor of VSV-G, limits the efficiency of lentiviral vector transduction. Sendai virus hemagglutinin-neuraminidase glycoproteins recognize terminal sialic acids on the host cell plasma membrane, facilitating viral entry. Here, we describe methods for lentiviral dual-pseudotyping with VSV-G and Sendai virus hemagglutinin-neuraminidase to broaden viral tropism.
巻・号 2974
ページ 51-59
公開日 2026-1-1
DOI 10.1007/978-1-0716-4807-0_5
PMID 41273640
MeSH Cell Line Gene Transfer Techniques* Genetic Vectors* / genetics HEK293 Cells HN Protein* / genetics HN Protein* / metabolism Humans Lentivirus* / genetics Membrane Glycoproteins Sendai virus* / genetics Transduction, Genetic / methods Viral Envelope Proteins* / genetics Viral Envelope Proteins* / metabolism Viral Tropism
リソース情報
遺伝子材料 CS-CA-GFP (RDB05964) pCAG-HIVgp (RDB04394) pRSV-Rev (RDB08121) pCMV-VSV-G (RDB04392)