brownian dynamics simulation of nucleocytoplasmic transport a coarse-grained model for the functional state of the nuclear pore complex布朗动力学模拟核质运输的粗粒度模型的功能状态核孔复合体.pdfVIP

brownian dynamics simulation of nucleocytoplasmic transport a coarse-grained model for the functional state of the nuclear pore complex布朗动力学模拟核质运输的粗粒度模型的功能状态核孔复合体.pdf

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brownian dynamics simulation of nucleocytoplasmic transport a coarse-grained model for the functional state of the nuclear pore complex布朗动力学模拟核质运输的粗粒度模型的功能状态核孔复合体

Brownian Dynamics Simulation of Nucleocytoplasmic Transport: A Coarse-Grained Model for the Functional State of the Nuclear Pore Complex Ruhollah Moussavi-Baygi, Yousef Jamali, Reza Karimi, Mohammad R. K. Mofrad* Molecular Cell Biomechanics Laboratory, Department of Bioengineering, University of California, Berkeley, California, United States of America Abstract The nuclear pore complex (NPC) regulates molecular traffic across the nuclear envelope (NE). Selective transport happens on the order of milliseconds and the length scale of tens of nanometers; however, the transport mechanism remains elusive. Central to the transport process is the hydrophobic interactions between karyopherins (kaps) and Phe-Gly (FG) repeat domains. Taking into account the polymeric nature of FG-repeats grafted on the elastic structure of the NPC, and the kap-FG hydrophobic affinity, we have established a coarse-grained model of the NPC structure that mimics nucleocytoplasmic transport. To establish a foundation for future works, the methodology and biophysical rationale behind the model is explained in details. The model predicts that the first-passage time of a 15 nm cargo-complex is about 2.6 60.13 ms with an inverse Gaussian distribution for statistically adequate number of independent Brownian dynamics simulations. Moreover, the cargo-complex is primarily attached to the channel wall where it interacts with the FG-layer as it passes through the central channel. The kap-FG hydrophobic interaction is highly dynamic and fast, which ensures an efficient translocation through the NPC. Further, almost all eight hydrophobic binding spots on kap-b are occupied simultaneously during transport. Finally, as opposed to intact NPCs, cytoplasmic filaments-deficient NPCs show a high degree of permeability to inert cargos, implying the defining role of cy

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