Department of Chemistry and Biochemistry , Auburn University , Auburn , Alabama 36849 , United States.
Langmuir. 2018 Jun 26;34(25):7509-7518. doi: 10.1021/acs.langmuir.8b00798. Epub 2018 Jun 12.
This article reports a high-yield procedure for preparing microsized (giant) Janus liposomes via gel-assisted lipid swelling and clustering behavior of these liposomes directed by biotin-avidin affinity binding. Confocal fluorescence microscopy reveals in detail that these new lipid colloidal particles display broken symmetry and heterogeneous surface chemistry similar to other types of Janus particles. An optimized formation procedure is presented, which reproducibly yields large liposome populations dominated by a single-domain configuration. This work further demonstrates that biotin-conjugated 1,2-dioleoyl- sn-glycero-3-phosphoethanolamine preferentially partitions into the liquid-disordered phase of the lipid matrix, rendering these Janus liposomes asymmetrical binding capacity toward avidin. This affinity binding drives irreversible and domain-specific cluster formation among Janus liposomes, whose structure and size are found to depend on the domain configuration of individual liposomes and incubation time.
本文报道了一种高产率的方法,通过凝胶辅助脂质溶胀和生物素-亲和素结合对这些脂质体的聚类行为,制备微尺寸(巨型)Janus 脂质体。共焦荧光显微镜详细揭示了这些新的脂质胶体粒子显示出破缺的对称性和与其他类型的 Janus 粒子相似的异质表面化学。提出了一种优化的形成程序,可重复性地产生以单畴构型为主的大脂质体群体。这项工作进一步表明,生物素缀合的 1,2-二油酰基-sn-甘油-3-磷酸乙醇胺优先分配到脂质基质的无序相中,使这些 Janus 脂质体对亲和素有不对称的结合能力。这种亲和结合驱动 Janus 脂质体之间不可逆和特定于结构域的聚集形成,其结构和大小取决于各个脂质体的结构域构型和孵育时间。