Effects of linker sequences on vesicle fusion mediated by lipid-anchored DNA oligonucleotides

被引:238
作者
Chan, Yee-Hung M. [1 ]
van Lengerich, Bettina [1 ]
Boxer, Steven G. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
DNA machine; synthetic biology; SINGLE-STRANDED-DNA; MEMBRANE-FUSION; SNARE PROTEINS; BILAYERS; DETERMINANTS; CHOLESTEROL; DYNAMICS; KINETICS; DEPENDS; LENGTH;
D O I
10.1073/pnas.0812356106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Synthetic lipid-oligonucleotide conjugates inserted into lipid vesicles mediate fusion when one population of vesicles displays the 5'-coupled conjugate and the other the 3'-coupled conjugate, so that anti-parallel hybridization allows the membrane surfaces to come into close proximity. Improved assays show that lipid mixing proceeds more quickly and to a much greater extent than content mixing, suggesting the latter is rate limiting. To test the effect of membrane-membrane spacing on fusion, a series of conjugates was constructed by adding 2-24 noncomplementary bases at the membrane-proximal ends of two complementary sequences. Increasing linker lengths generally resulted in progressively reduced rates and extents of lipid and content mixing, in contrast to higher vesicle docking rates. The relatively flexible, single-stranded DNA linker facilitates docking but allows greater spacing between the vesicles after docking, thus making the transition into fusion less probable, but not preventing it altogether. These experiments demonstrate the utility of DNA as a model system for fusion proteins, where sequence can easily be modified to systematically probe the effect of distance between bilayers in the fusion reaction.
引用
收藏
页码:979 / 984
页数:6
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