Institute for Theoretical Physics, Heidelberg University, Philosophenweg 19, 69120 Heidelberg, Germany and BioQuant, Heidelberg University, Im Neuenheimer Feld 267, 69120 Heidelberg, Germany.
Institut Charles Sadron UPR22-CNRS, 67034 Strasbourg, France and Institute Theory of Polymers, Leibniz-Institute of Polymer Research, D-01069 Dresden, Germany.
Phys Rev Lett. 2021 May 28;126(21):218101. doi: 10.1103/PhysRevLett.126.218101.
While often believed to be a passive agent that merely exploits its host's metabolism, the influenza virus has recently been shown to actively move across glycan-coated surfaces. This form of enzymatically driven surface motility is currently not well understood and has been loosely linked to burnt-bridge Brownian ratchet mechanisms. Starting from known properties of influenza's spike proteins, we develop a physical model that quantitatively describes the observed motility. It predicts a collectively emerging dynamics of spike proteins and surface-bound ligands that combined with the virus' geometry give rise to a self-organized rolling propulsion. We show that in contrast to a Brownian ratchet, the rotary spike drive is not fluctuation driven but operates optimally as a macroscopic engine in the deterministic regime. The mechanism also applies to relatives of influenza and to man-made analogs like DNA monowheels and should give guidelines for their optimization.
虽然流感病毒通常被认为是一种被动的因子,仅仅利用宿主的新陈代谢,但最近它已被证明能够主动在糖蛋白覆盖的表面上移动。这种酶驱动的表面迁移形式目前还不太清楚,并且与烧桥布朗棘轮机制松散地联系在一起。从流感刺突蛋白的已知特性出发,我们开发了一个物理模型,该模型定量描述了所观察到的运动。它预测了刺突蛋白和表面结合配体的集体涌现动力学,再加上病毒的几何形状,导致了一种自组织的滚动推进。我们表明,与布朗棘轮不同,旋转刺突驱动不是由涨落驱动,而是作为一种宏观发动机在确定性状态下最优地运行。该机制也适用于流感的相关病毒以及人工模拟物,如 DNA 单轮,并且应该为它们的优化提供指导。