Engineering novel cell surface receptors for virus-mediated gene transfer

被引:72
作者
Lee, JH
Baker, TJ
Mahal, LK
Zabner, J
Bertozzi, CR
Wiemer, DF
Welsh, MJ
机构
[1] Univ Iowa, Coll Med, Howard Hughes Med Inst, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Physiol & Biophys, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Lab, Dept Chem, Berkeley, CA 94720 USA
[6] Univ Calif Berkeley, Lawrence Berkeley Lab, Ctr Adv Mat, Berkeley, CA 94720 USA
关键词
D O I
10.1074/jbc.274.31.21878
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The absence of viral receptors is a major barrier to efficient gene transfer in many cells. To overcome this barrier, we developed an artificial receptor based on expression of a novel sugar, We fed cells an unnatural monosaccharide, a modified mannosamine that replaced the acetyl group with a levulinate group (ManLev), ManLev was metabolized and incorporated into cell-surface glycoconjugates. The synthetic sugar decorated the cell surface with a unique ketone group that served as a foundation on which we built an adenovirus receptor by covalently binding biotin hydrazide to the ketone. The artificial receptor enhanced adenoviral vector binding and gene transfer to cells that are relatively resistant to adenovirus infection. These data are the first to suggest the feasibility of a strategy that improves the efficiency of gene transfer by using the biosynthetic machinery of the cell to engineer novel sugars on the cell surface.
引用
收藏
页码:21878 / 21884
页数:7
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