DNA Hybridization-Mediated Liposome Fusion at the Aqueous Liquid Crystal Interface.
DNA Hybridization-Mediated Liposome Fusion at the Aqueous Liquid Crystal Interface.
复制标题
DNA杂交介导的脂质体融合在水性液晶界面处。
DOI:
10.1002/adfm.201303885
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发表时间:
2014-06-04
影响因子:
19
通讯作者:
Schwartz, Daniel K.
中科院分区:
文献类型:
--
作者:
Noonan, Patrick S.;Mohan, Praveena;Goodwin, Andrew P.;Schwartz, Daniel K.
The prominence of receptor-mediated bilayer fusion in cellular biology motivates development of biomimetic strategies for studying fusogenic mechanisms. An approach is reported here for monitoring receptor-mediated fusion that exploits the unique physical and optical properties of liquid crystals (LC). PEG-functionalized lipids are used to create an interfacial environment capable of inhibiting spontaneous liposome fusion with an aqueous/LC interface. Then, DNA hybridization between oligonucleotides within bulk phase liposomes and a PEG-lipid monolayer at an aqueous/LC interface is exploited to induce receptor-mediated liposome fusion. These hybridization events induce strain within the liposome bilayer, promote lipid mixing with the LC interface, and consequently create an interfacial environment favoring re-orientation of the LC to a homeotropic (perpendicular) state. Furthermore, the bi-functionality of aptamers is exploited to modulate DNA hybridization-mediated liposome fusion by regulating the availability of the appropriate ligand (i.e., thrombin). Here, a LC-based approach for monitoring receptor (i.e., DNA hybridization)-mediated liposome fusion is demonstrated, liposome properties that dictate fusion dynamics are explored, and an example of how this approach may be used in a biosensing scheme is provided.
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