Maestro Armando, Zaccai Nathan R, Gonzalez-Martinez Juan F, Sanchez-Puga Pablo, Tajuelo Javier, Rubio Miguel A, Santamaria Andreas, Carrascosa-Tejedor Javier, Pereira Daniel, Marín-Montesinos Ildefonso, Gutfreund Philipp, Campbell Richard, Kotar Jurij, Kelly Bernard T, Cicuta Pietro, Owen David J
Centro de Fı́sica de Materiales (CSIC, UPV/EHU) - Materials Physics Center MPC, Paseo Manuel de Lardizabal 5, San Sebastián, Spain.
IKERBASQUE-Basque Foundation for Science, Bilbao, Spain.
Commun Biol. 2025 Aug 12;8(1):1196. doi: 10.1038/s42003-025-08597-5.
Clathrin-mediated endocytosis (CME), the main mechanism for swift, selective protein uptake in eukaryotic cells, initiates with adaptor protein AP2 recruitment to the plasma membrane (PM). AP2 recognizes PM-associated PtdIns(4,5)P2 and protein cargo for internalization. Nonetheless, many aspects of this process remain unclear due to their in vivo complexity. Here, a thermodynamic and time-resolved structural analysis of AP2 binding to different biomimetic PM was undertaken under physiological conditions using a combination of neutron reflectometry, interfacial tensiometry and rheology, and atomic force microscopy. The resultant in vitro data replicated previous in vivo observations, as well as yielded biophysical insights into normal and aborted CME. The presence of cargo may not be pivotal for the "activating" conformational change of AP2. However, the presence of cargo extends AP2's residence time on the membrane surface, due to slower on- and off-rates, thereby tentatively giving sufficient time for CME to proceed fully. Moreover, upon interaction with AP2, phospholipid lateral diffusion decreases markedly, inducing a gel phase attributed to creating a percolated network involving AP2 on the membrane, which could potentially serve as a mechanism for modulating subsequent clathrin binding. The subsequent clathrin polymerization at the membrane is dependent on the AP2's clathrin binding sequence.
网格蛋白介导的内吞作用(CME)是真核细胞中快速、选择性摄取蛋白质的主要机制,它始于衔接蛋白AP2被招募到质膜(PM)。AP2识别与质膜相关的磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P2)和用于内化的蛋白质货物。然而,由于该过程在体内的复杂性,其许多方面仍不清楚。在此,利用中子反射率、界面张力测定法和流变学以及原子力显微镜相结合的方法,在生理条件下对AP2与不同仿生质膜的结合进行了热力学和时间分辨结构分析。所得的体外数据重现了先前的体内观察结果,并对正常和异常的CME产生了生物物理方面的见解。货物的存在可能对于AP2的“激活”构象变化并非关键因素。然而,货物的存在延长了AP2在膜表面的停留时间,这是由于其结合和解离速率较慢,从而暂时为CME的充分进行提供了足够的时间。此外,与AP2相互作用后,磷脂的侧向扩散显著降低,诱导了一种凝胶相,这归因于在膜上形成了一个涉及AP2的渗透网络,这可能潜在地作为调节后续网格蛋白结合的一种机制。随后膜上的网格蛋白聚合取决于AP2的网格蛋白结合序列。