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- W2061327160 abstract "Abstract Background The application of serotype 5 adenoviruses (Ad5) in macrophages is hampered by the absence of the endogenous coxsackie adenovirus receptor (CAR). Methods To overcome this limitation, we first generated a linker protein consisting of the virus‐binding domain of CAR and the C‐terminus of avidin. Second, to target macrophages, this linker protein was equipped with the biotinylated (bio) oligonucleotide dA 6 G 10 , which was previously shown to display a high affinity for the scavenger receptor A (SR‐A). Results As compared to nontargeted virus, the linker protein equipped with bio‐dA 6 G 10 showed a 500‐fold increased reporter gene expression in mouse macrophage RAW264.7 cells. A linker protein equipped with a bio‐dA 16 control oligonucleotide was inactive. Moreover, the bio‐dA 6 G 10 ‐equipped linker showed a 390‐fold increased luciferase expression in the macrophage cell line J774 and 276‐ and 150‐fold increased reporter gene expression in primary peritoneal and bone marrow (BM)‐derived macrophages, respectively. Using BM‐derived macrophages from SR‐A knockout mice, it was shown that the dA 6 G 10 ‐mediated uptake is predominantly SR‐A‐mediated. Conclusions Thus, we have developed a novel tool to link biotinylated ligands to a virus‐binding fragment of CAR and have exploited this linker protein to extend the applicability of Ad5 to infect transformed and primary macrophages. Copyright © 2006 John Wiley & Sons, Ltd." @default.
- W2061327160 created "2016-06-24" @default.
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- W2061327160 date "2006-03-13" @default.
- W2061327160 modified "2023-10-12" @default.
- W2061327160 title "Specific and efficient targeting of adenovirus vectors to macrophages: application of a fusion protein between an adenovirus-binding fragment and avidin, linked to a biotinylated oligonucleotide" @default.
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- W2061327160 doi "https://doi.org/10.1002/jgm.895" @default.
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