Szymczak Piotr
Institute of Theoretical Physics, Faculty of Physics, University of Warsaw, Warsaw, Poland.
Sci Rep. 2016 Mar 21;6:21702. doi: 10.1038/srep21702.
Proteins need to be unfolded when translocated through the pores in mitochondrial and other cellular membranes. Knotted proteins, however, might get stuck during this process, jamming the pore, since the diameter of the pore is smaller than the size of maximally tightened knot. The jamming probability dramatically increases as the magnitude of the driving force exceeds a critical value, Fc. In this numerical study, we show that for deep knots Fc lies below the force range over which molecular import motors operate, which suggest that in these cases the knots will tighten and block the pores. Next, we show how such topological traps might be prevented by using a pulling protocol of a repetitive, on-off character. Such a repetitive pulling is biologically relevant, since the mitochondrial import motor, like other molecular motors transforms chemical energy into directed motions via nucleotide-hydrolysis-mediated conformational changes, which are cyclic in character.
蛋白质在线粒体和其他细胞膜的孔道中转运时需要解折叠。然而,打结的蛋白质在这个过程中可能会卡住,堵塞孔道,因为孔道的直径小于最大收紧结的尺寸。当驱动力的大小超过临界值Fc时,堵塞概率会急剧增加。在这项数值研究中,我们表明,对于深结,Fc处于分子输入马达运作的力范围之下,这表明在这些情况下,结会收紧并堵塞孔道。接下来,我们展示了如何通过使用具有重复开关特性的拉动方案来防止这种拓扑陷阱。这种重复拉动在生物学上是相关的,因为线粒体输入马达与其他分子马达一样,通过核苷酸水解介导的构象变化将化学能转化为定向运动,而这种变化具有循环性质。