颗粒流和完整的细胞外黏液纳米纤维的力学测试揭示了弹性力在硅藻运动中的作用。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Physical biology Pub Date : 2022-07-14 DOI:10.1088/1478-3975/ac7d30
Braulio Gutiérrez-Medina, Ana Iris Peña Maldonado, Jessica Viridiana García-Meza
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引用次数: 3

摘要

硅藻是一种单细胞微藻,具有坚硬的细胞壁,能够通过被称为“图”的中心狭缝释放纳米聚合物纤维在表面上滑动。在这里,我们考虑的模型是对硅藻滑翔涉及的两个互补方面进行定量研究。使用视频显微镜和自动图像分析,我们测量了测试珠在硅藻raphe(粒子流)处被细胞外聚合物(EPS)纤维拉拽时的运动。发现了粒子速度的多模态分布,证明了高速和加速的短时间事件(称为突然运动)的出现,并表明不同的机制有助于在滑翔过程中设定硅藻速度。此外,我们使用光镊获得胞外硅藻纳米纤维的力扩展记录;聚合物弹性的蠕虫状链模型很好地描述了记录。与先前基于施加变性力(在nN范围内)的研究相反,施加低力(高达6 pN)和使用使我们能够获得完整纤维的持久长度。通过这些测量,估计了EPS纤维的半径和弹性常数等力学参数。此外,通过将粒子流建模为与阻尼器平行的弹簧,我们表明,纤维从珠子脱离(弹性断裂)后释放机械能所涉及的时间与我们对突然运动的观察一致。我们得出结论,滑行硅藻所表现出的平稳和突然运动分别对应于分子马达和弹性断裂,从而为硅藻运动背后的当前力学模型提供了定量元素。
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Mechanical testing of particle streaming and intact extracellular mucilage nanofibers reveal a role of elastic force in diatom motility.

Diatoms are unicellular microalgae with a rigid cell wall, able to glide on surfaces by releasing nanopolymeric fibers through central slits known as raphes. Here we consider the modelNitszchia communisto perform quantitative studies on two complementary aspects involved in diatom gliding. Using video microscopy and automated image analysis, we measure the motion of test beads as they are pulled by extracellular polymeric substances (EPS) fibers at the diatom raphe (particle streaming). A multimodal distribution of particle speed is found, evidencing the appearance of short-time events of high speed and acceleration (known as jerky motion) and suggesting that different mechanisms contribute to set diatom velocity during gliding. Furthermore, we use optical tweezers to obtain force-extension records for extracellular diatom nanofibers; records are well described by the worm-like chain model of polymer elasticity. In contrast to previous studies based on application of denaturing force (in the nN regime), application of low force (up to 6 pN) and using enable us to obtain the persistence length of intact fibers. From these measurements, mechanical parameters of EPS fibers such as radius and elastic constant are estimated. Furthermore, by modeling particle streaming as a spring in parallel with a dashpot, we show that the time involved in the release of mechanical energy after fiber detachment from beads (elastic snapping) agrees with our observations of jerky motion. We conclude that the smooth and jerky motions displayed by gliding diatoms correspond to molecular motors and elastic snapping, respectively, thus providing quantitative elements that incorporate to current models of the mechanics behind diatom locomotion.

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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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