Qiu Jie, Ma Dongfei, You Xin, Jia Qi, Hu Shuxin, Xu Cheng, Cao Binglong, Yang Kai, Han Weijing, Lu Ying, Yuan Bing, Li Ming
Songshan Lake Materials Laboratory, Dongguan, Guangdong 523808, China.
Center for Soft Condensed Matter Physics and Interdisciplinary Research, School of Physical Science and Technology, Soochow University, Suzhou, Jiangsu 215006, China.
ACS Nano. 2025 Apr 29;19(16):15685-15697. doi: 10.1021/acsnano.4c18301. Epub 2025 Apr 18.
The pH-triggered structural transition and translocation of the pH low-insertion peptide (pHLIP) across cell membranes, facilitated by its distinct protonation property, render it a valuable model for investigating the membrane insertion mechanism of molecules. This capability also holds significant promise for advancements in cancer diagnosis and transmembrane transport. In this study, we investigated the dynamics of membrane insertion of wild-type pHLIP and its three variants using real-time tracking of single-peptide translocation kinetics. We identified three distinct metastable molecular conformations of pHLIPs within the bilayer, referred to as ″kinetic intermediate states″ at varying depths within the bilayer. These metastable conformations were observed during both the pH-triggered membrane insertion process and at intervening pH levels (between 7.4 and 5.0). Over time following a decrease in pH, these molecular conformations gradually transitioned with an increasing number of peptides shifting from a horizontally bound state to an inserted state, with a gradual deepening of their depth until equilibrium was reached around 10 min. Additionally, all individual peptides within the membrane experienced subsecond level kinetic fluctuations. Modifications such as P20G increased penetration depth without affecting the insertion process, whereas truncating residues D and E from the C-terminal accelerated membrane insertion speed but reduced penetration depth. Our findings elucidate how residue protonation-driven conformational changes influence peptide dynamics during membrane insertion, thereby providing insights for designing advanced drug delivery systems.
pH低插入肽(pHLIP)因其独特的质子化特性而在细胞膜上发生pH触发的结构转变和转运,这使其成为研究分子膜插入机制的有价值模型。这种能力在癌症诊断和跨膜运输方面也具有重大的应用前景。在本研究中,我们通过实时跟踪单肽转运动力学,研究了野生型pHLIP及其三种变体的膜插入动力学。我们在双层膜中确定了pHLIP的三种不同的亚稳分子构象,在双层膜内不同深度处称为“动力学中间态”。在pH触发的膜插入过程以及中间pH水平(7.4至5.0之间)均观察到了这些亚稳构象。随着pH值降低,这些分子构象随时间逐渐转变,越来越多的肽从水平结合状态转变为插入状态,其深度逐渐加深,直至约10分钟达到平衡。此外,膜内所有单个肽都经历了亚秒级的动力学波动。诸如P20G之类的修饰增加了穿透深度而不影响插入过程,而从C末端截短残基D和E则加快了膜插入速度,但降低了穿透深度。我们的研究结果阐明了残基质子化驱动的构象变化如何影响膜插入过程中的肽动力学,从而为设计先进的药物递送系统提供了见解。