Niroomand Hanieh, Venkatesan Guru A, Sarles Stephen A, Mukherjee Dibyendu, Khomami Bamin
Sustainable Energy Education and Research Center (SEERC), University of Tennessee, Knoxville, TN, USA.
Department of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, TN, USA.
J Membr Biol. 2016 Aug;249(4):523-38. doi: 10.1007/s00232-016-9894-1. Epub 2016 Apr 12.
We investigate the phase transition stages for detergent-mediated liposome solubilization of bio-mimetic membranes with the motivation of integrating membrane-bound Photosystem I into bio-hybrid opto-electronic devices. To this end, the interaction of two non-ionic detergents n-dodecyl-β-D-maltoside (DDM) and Triton X-100 (TX-100) with two types of phospholipids, namely DPhPC (1,2-diphytanoyl-sn-glycero-3-phosphocholine) and DPPG (1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol)), are examined. Specifically, solubilization processes for large unilamellar liposomes are studied with the aid of turbidity measurements, dynamic light scattering, and cryo-transmission electron microscopy imaging. Our results indicate that the solubilization process is well depicted by a three-stage model, wherein the lamellar-to-micellar transitions for DPhPC liposomes are dictated by the critical detergent/phospholipid ratios. The solubilization of DPhPC by DDM is devoid of formation of a "gel-like" phase. Furthermore, our results indicate that DDM is a stable candidate for DPhPC solubilization and proteoliposome formation. Finally, although the solubilization of DPPG with DDM indicated the familiar three-stage process, the same process with TX-100 indicate structural deformation of vesicles into complex network of kinetically trapped micro- and nanostructured arrangements of lipid bilayers.
我们研究了去污剂介导的仿生膜脂质体溶解的相变阶段,目的是将膜结合的光系统I整合到生物混合光电器件中。为此,研究了两种非离子去污剂正十二烷基-β-D-麦芽糖苷(DDM)和吐温X-100(TX-100)与两种磷脂,即二植酰磷脂酰胆碱(DPhPC,1,2-二植酰-sn-甘油-3-磷酸胆碱)和二棕榈酰磷脂酰甘油(DPPG,1,2-二棕榈酰-sn-甘油-3-磷酸-(1'-rac-甘油))之间的相互作用。具体而言,借助浊度测量、动态光散射和冷冻透射电子显微镜成像研究了大单层脂质体的溶解过程。我们的结果表明,溶解过程可以用一个三阶段模型很好地描述,其中DPhPC脂质体从片层到胶束的转变由临界去污剂/磷脂比决定。DDM对DPhPC的溶解没有形成“凝胶状”相。此外,我们的结果表明,DDM是溶解DPhPC和形成蛋白脂质体的稳定候选物。最后,尽管DDM对DPPG的溶解显示出常见的三阶段过程,但TX-100对DPPG的溶解过程表明囊泡结构变形为脂质双层的动力学捕获的微结构和纳米结构排列的复杂网络。