Basu Jashaswi, Soni Aman, Athale Chaitanya A
Division of Biology, IISER Pune, Pashan, Pune, India.
Division of Biology, IISER Pune, Pashan, Pune, India.
Biophys J. 2025 Mar 4;124(5):789-806. doi: 10.1016/j.bpj.2025.01.020. Epub 2025 Jan 29.
The polymerization of cytoskeletal filaments is regulated by both biochemical pathways, as well as physical factors such as crowding. The effect of crowding in vivo emerges from the density of intracellular components. Due to the complexity of the intracellular environment, most studies are based on either in vitro reconstitution or theory. Crowding agent (crowdants) size has been shown to influence polymerization of both actin and microtubules (MTs). Previously, the elongation rates of MT dynamics observed at single filament scale were reported to decrease with increasing concentrations of small but not large crowdants, and this correlated with in vivo viscosity increases. However, the exact nature of the connection between viscosity, crowdant size, nucleation, and MT elongation has remained unclear. Here, we use in vitro reconstitution of bulk MT polymerization kinetics and microscopy to examine the collective effect of crowdant molecular weight, volume occupancy, and viscosity on elongation and spontaneous polymerization. We find MT elongation rates obtained from bulk polymerization decrease in the presence of multiple low-molecular weight (LMW) crowdants, while increasing with high-molecular weight (HMW) crowdants. Lattice Monte Carlo simulations of an effective model of collective polymerization demonstrate reduced polymerization rates arise due to decrease in monomer diffusion due to small-sized crowdants. However, MT polymerization in the absence of nucleators, de novo, shows a crowdant size independence of polymerization rate and critical concentration, depending solely on concentration of the crowdant. In microscopy, we find LMW crowdants result in short but many filaments, while HMW crowdants increase filament density, but have little effect on lengths. The effect of crowdant volume fraction ϕ and size in de novo polymerization match simulations, demonstrating crowdants affect elongation independent of nucleation. Thus, the effect of viscosity on collective MT dynamics, i.e., filament numbers and lengths, shows crowdant size dependence for elongation, but independence for de novo polymerization.
细胞骨架丝的聚合受生化途径以及诸如拥挤等物理因素的调节。体内拥挤效应源于细胞内成分的密度。由于细胞内环境的复杂性,大多数研究基于体外重建或理论。已表明拥挤剂(crowdants)的大小会影响肌动蛋白和微管(MTs)的聚合。此前,据报道在单丝尺度观察到的MT动力学伸长率会随着小拥挤剂而非大拥挤剂浓度的增加而降低,这与体内粘度增加相关。然而,粘度、拥挤剂大小、成核和MT伸长之间联系的确切性质仍不清楚。在这里,我们使用体外重建的大量MT聚合动力学和显微镜技术来研究拥挤剂分子量、体积占有率和粘度对伸长和自发聚合的集体效应。我们发现,在存在多种低分子量(LMW)拥挤剂的情况下,从大量聚合获得的MT伸长率会降低,而在高分子量(HMW)拥挤剂存在时则会增加。集体聚合有效模型的晶格蒙特卡罗模拟表明,由于小尺寸拥挤剂导致单体扩散减少,聚合速率降低。然而,在没有成核剂的情况下从头开始的MT聚合显示,聚合速率和临界浓度与拥挤剂大小无关,仅取决于拥挤剂的浓度。在显微镜观察中,我们发现LMW拥挤剂会导致短而多的丝状物,而HMW拥挤剂会增加丝状物密度,但对长度影响很小。拥挤剂体积分数ϕ和大小在从头聚合中的作用与模拟结果相符,表明拥挤剂影响伸长而与成核无关。因此,粘度对集体MT动力学(即丝状物数量和长度)的影响表明,拥挤剂大小对伸长有依赖性,但对从头聚合则无依赖性。