Erickson Austen M, Henry Bruce I, Murray John M, Klasse Per Johan, Angstmann Christopher N
School of Mathematics and Statistics, UNSW Australia, Sydney, New South Wales, Australia.
Department of Microbiology and Immunology, Weill Cornell Medical College, Cornell University, New York, New York.
Biophys J. 2015 Jul 7;109(1):164-72. doi: 10.1016/j.bpj.2015.05.034.
Particle-tracking experiments focusing on virions or nanoparticles in mucus have measured mean-square displacements and reported diffusion coefficients that are orders of magnitude smaller than the diffusion coefficients of such particles in water. Accurate description of this subdiffusion is important to properly estimate the likelihood of virions traversing the mucus boundary layer and infecting cells in the epithelium. However, there are several candidate models for diffusion that can fit experimental measurements of mean-square displacements. We show that these models yield very different estimates for the time taken for subdiffusive virions to traverse through a mucus layer. We explain why fits of subdiffusive mean-square displacements to standard diffusion models may be misleading. Relevant to human immunodeficiency virus infection, using computational methods for fractional subdiffusion, we show that subdiffusion in normal acidic mucus provides a more effective barrier against infection than previously thought. By contrast, the neutralization of the mucus by alkaline semen, after sexual intercourse, allows virions to cross the mucus layer and reach the epithelium in a short timeframe. The computed barrier protection from fractional subdiffusion is some orders of magnitude greater than that derived by fitting standard models of diffusion to subdiffusive data.
聚焦于黏液中病毒粒子或纳米颗粒的粒子追踪实验测量了均方位移,并报告了扩散系数,这些扩散系数比此类粒子在水中的扩散系数小几个数量级。准确描述这种亚扩散对于正确估计病毒粒子穿过黏液边界层并感染上皮细胞的可能性很重要。然而,有几种扩散候选模型可以拟合均方位移的实验测量值。我们表明,这些模型对亚扩散病毒粒子穿过黏液层所需的时间给出了非常不同的估计。我们解释了为什么将亚扩散均方位移拟合到标准扩散模型可能会产生误导。与人类免疫缺陷病毒感染相关,使用分数亚扩散的计算方法,我们表明正常酸性黏液中的亚扩散提供了比以前认为的更有效的感染屏障。相比之下,性交后碱性精液对黏液的中和作用使病毒粒子能够在短时间内穿过黏液层并到达上皮细胞。通过分数亚扩散计算得出的屏障保护比通过将标准扩散模型拟合到亚扩散数据得出的保护大几个数量级。