School of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Department of Bionano Technology, Hanyang University, Ansan 15588, Republic of Korea.
J Colloid Interface Sci. 2020 Mar 1;561:318-326. doi: 10.1016/j.jcis.2019.10.109. Epub 2019 Nov 1.
We report a facile, but robust approach to fabricate structurally stable giant unilamellar vesicles (GUVs), on which a 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) bilayer membrane was made rigid by introducing amphiphilic block polymers. Particularly, we found that lateral co-assembly of an amphiphilic triblock copolymer (ATC) structured with a hydrophobic middle block and long molecular weight (20 K g/mol) hydrophilic end blocks remarkably enhanced the stretching modulus (k) of GUVs. When the membrane composition was optimized, the k value of ATC-hybridized GUVs increased to 6.2 × 10 Pa, which was approximately 10-fold higher than that of DPPC GUVs, thus leading to a much longer half-life. Moreover, we demonstrated that our ATC-hybridized GUVs enabled development of a fascinating vesicular model, which shows great potential as a structurally stable cell membrane mimic.
我们报告了一种简单但稳健的方法来制备结构稳定的巨大单层囊泡(GUVs),在这些囊泡上,通过引入两亲性嵌段聚合物使 1,2-二棕榈酰基-sn-甘油-3-磷酸胆碱(DPPC)双层膜变硬。特别地,我们发现具有疏水中间块和长分子量(20K g/mol)亲水端块的两亲性三嵌段共聚物(ATC)的侧向共组装显着提高了 GUVs 的拉伸模量(k)。当优化膜组成时,ATC 杂交 GUVs 的 k 值增加到 6.2×10 Pa,约为 DPPC GUVs 的 10 倍,从而导致半衰期大大延长。此外,我们证明了我们的 ATC 杂交 GUVs 能够开发出一种迷人的囊泡模型,该模型作为结构稳定的细胞膜模拟物具有很大的潜力。