Department of Physics, University of Cagliari, 09042 Monserrato, Italy.
Phys Chem Chem Phys. 2021 Sep 14;23(34):18461-18474. doi: 10.1039/d1cp02947a. Epub 2021 Aug 24.
Subcellular and organellar mechanisms have manifested a prominent importance for a broad variety of processes that maintain cellular life at its most basic level. Mammalian two-pore channels (TPCs) appear to be cornerstones of these processes in endo-lysosomes by controlling delicate ion-concentrations in their interiors. With evolutionary remarkable architecture and one-of-a-kind selectivity filter, TPCs are an extremely attractive topic per se. In the light of the current COVID-19 pandemic, hTPC2 emerges to be more than attractive. As a key regulator of the endocytosis pathway, it is potentially essential for diverse viral infections in humans, as demonstrated. Here, by means of multiscale molecular simulations, we propose a model of sodium transport from the lumen to the cytosol where the central cavity works as a reservoir. Since the inhibition of hTPC2 is proven to stop SARS-CoV2 in vitro, shedding light on the hTPC2 function and mechanism is the first step towards the selection of potential inhibiting candidates.
亚细胞和细胞器机制对于维持细胞最基本生命水平的各种过程表现出重要作用。哺乳动物双孔通道(TPC)似乎是内溶酶体中这些过程的基石,通过控制内部精细的离子浓度。TPC 具有进化上显著的结构和独一无二的选择性过滤器,本身就是一个极具吸引力的话题。鉴于当前的 COVID-19 大流行,hTPC2 变得更加有吸引力。作为内吞作用途径的关键调节剂,它对于人类的多种病毒感染可能是必不可少的,正如所证明的那样。在这里,我们通过多尺度分子模拟,提出了一个从腔到细胞质的钠离子转运模型,其中中央腔作为一个储库。由于 hTPC2 的抑制已被证明可以阻止 SARS-CoV2 在体外复制,因此阐明 hTPC2 的功能和机制是选择潜在抑制候选物的第一步。