Al Kury Lina T, Papandreou Dimitrios, Hurmach Vasyl V, Dryn Dariia O, Melnyk Mariia I, Platonov Maxim O, Prylutskyy Yuriy I, Ritter Uwe, Scharff Peter, Zholos Alexander V
College of Natural and Health Sciences, Zayed University, Abu Dhabi 144534, United Arab Emirates.
ESC "Institute of Biology and Medicine", Taras Shevchenko National University of Kyiv, 64 Volodymyrska Str., 01601 Kyiv, Ukraine.
Nanomaterials (Basel). 2021 Dec 16;11(12):3410. doi: 10.3390/nano11123410.
Single-walled carbon nanotubes (SWCNTs) are characterized by a combination of rather unique physical and chemical properties, which makes them interesting biocompatible nanostructured materials for various applications, including in the biomedical field. SWCNTs are not inert carriers of drug molecules, as they may interact with various biological macromolecules, including ion channels. To investigate the mechanisms of the inhibitory effects of SWCNTs on the muscarinic receptor cation current (mI, induced by intracellular GTPγs (200 μM), in isolated mouse ileal myocytes, we have used the patch-clamp method in the whole-cell configuration. Here, we use molecular docking/molecular dynamics simulations and direct patch-clamp recordings of whole-cell currents to show that SWCNTs, purified and functionalized by carboxylation in water suspension containing single SWCNTs with a diameter of 0.5-1.5 nm, can inhibit mI, which is mainly carried by TRPC4 cation channels in ileal smooth muscle cells, and is the main regulator of cholinergic excitation-contraction coupling in the small intestinal tract. This inhibition was voltage-independent and associated with a shortening of the mean open time of the channel. These results suggest that SWCNTs cause a direct blockage of the TRPC4 channel and may represent a novel class of TRPC4 modulators.
单壁碳纳米管(SWCNTs)具有相当独特的物理和化学性质,这使其成为用于各种应用(包括生物医学领域)的有趣的生物相容性纳米结构材料。SWCNTs并非药物分子的惰性载体,因为它们可能与包括离子通道在内的各种生物大分子相互作用。为了研究SWCNTs对分离的小鼠回肠肌细胞中毒蕈碱受体阳离子电流(mI,由细胞内GTPγs(200μM)诱导)的抑制作用机制,我们采用了全细胞模式的膜片钳方法。在此,我们使用分子对接/分子动力学模拟以及全细胞电流的直接膜片钳记录来表明,在含有直径为0.5 - 1.5 nm的单个SWCNTs的水悬浮液中通过羧化纯化和功能化的SWCNTs可以抑制mI,mI主要由回肠平滑肌细胞中的TRPC4阳离子通道介导,并且是小肠中胆碱能兴奋 - 收缩偶联的主要调节因子。这种抑制与电压无关,并且与通道平均开放时间的缩短有关。这些结果表明,SWCNTs导致TRPC4通道的直接阻断,并且可能代表一类新型的TRPC4调节剂。