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Bacterial Outer Membrane Porins as Electrostatic Nanosieves: Exploring Transport Rules of Small Polar Molecules

机译:细菌外膜悬料作为静电纳米尺寸:探索小极性分子的运输规则

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摘要

Transport of molecules through biological membranes is a fundamental process in biology, facilitated by selective channels and general pores. The architecture of some outer membrane pores in Gram-negative bacteria, common to other eukaryotic pores, suggests them as prototypes of electrostatically regulated nanosieve devices. In this study, we sensed the internal electrostatics of the two most abundant outer membrane channels of Escherichia coli, using norfloxacin as a dipolar probe in single molecule electrophysiology. The voltage dependence of the association rate constant of norfloxacin interacting with these nanochannels follows an exponential trend, unexpected for neutral molecules. We combined electrophysiology, channel mutagenesis, and enhanced sampling molecular dynamics simulations to explain this molecular mechanism. Voltage and temperature dependent ion current measurements allowed us to quantify the transversal electric field inside the channel as well as the distance where the applied potential drops. Finally, we proposed a general model for transport of polar molecules through these electrostatic nanosieves. Our model helps to further understand the basis for permeability in Gram-negative pathogens, contributing to fill in the innovation gap that has limited the discovery of effective antibiotics in the last 20 years.
机译:通过生物膜运输分子是生物学的基本过程,通过选择性通道和一般孔隙促进。对于其他真核毛孔共同的革兰氏阴性细菌的一些外膜孔的结构表明它们是静电纳米器件的原型。在这项研究中,我们在单分子电生理学中使用NORFLOXACINS作为双极探针感测了大肠杆菌的两个最丰富的外膜通道的内部静电。与这些纳米中的诺氟沙星相互作用的缔合率常数的电压依赖性遵循指数趋势,中性分子意外。我们组合电生理学,通​​道诱变,增强的采样分子动力学模拟以解释该分子机制。电压和温度相关的离子电流测量允许我们量化通道内的横向电场以及所施加电位下降的距离。最后,我们提出了一种用于通过这些静电纳米尺寸传输极性分子的一般模型。我们的型号有助于进一步了解革兰氏阴性病原体的渗透性的基础,有助于填补在过去20年中有限发现有效抗生素的创新缺口。

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