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光学陷阱牵引实验探测多体流体动力学相互作用。

Few-body hydrodynamic interactions probed by optical trap pulling experiment.

机构信息

Department of Bioinformatics and Life Science, Soongsil University, Seoul 06978, South Korea.

Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

J Chem Phys. 2023 Jul 14;159(2). doi: 10.1063/5.0148096.

DOI:10.1063/5.0148096
PMID:37431906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10338065/
Abstract

We study the hydrodynamic coupling of neighboring micro-beads placed in a multiple optical trap setup allowing us to precisely control the degree of coupling and directly measure time-dependent trajectories of entrained beads. We performed measurements on configurations with increasing complexity starting with a pair of entrained beads moving in one dimension, then in two dimensions, and finally a triplet of beads moving in two dimensions. The average experimental trajectories of a probe bead compare well with the theoretical computation, illustrating the role of viscous coupling and setting timescales for probe bead relaxation. The findings also provide direct experimental corroborations of hydrodynamic coupling at large, micrometer spatial scales and long, millisecond timescales, of relevance to, e.g., microfluidic device design and hydrodynamic-assisted colloidal assembly, improving the capability of optical tweezers, and understanding the coupling between micrometer-scale objects within a living cell.

摘要

我们研究了放置在多光学陷阱设置中的相邻微珠的流体动力耦合,这使我们能够精确控制耦合程度,并直接测量被捕获微珠的时变轨迹。我们从一对在一维空间中运动的被捕获微珠开始,然后在二维空间中,最后是在二维空间中运动的三个微珠,对越来越复杂的配置进行了测量。探针微珠的平均实验轨迹与理论计算吻合较好,说明了粘性耦合的作用,并为探针微珠的弛豫设置了时间尺度。这些发现还为在大的、微米级空间尺度和长的、毫秒级时间尺度上的流体动力耦合提供了直接的实验佐证,这与微流控器件设计和流体力学辅助胶体组装等有关,提高了光学镊子的能力,并有助于理解活细胞内微米级物体之间的耦合。

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1
Few-body hydrodynamic interactions probed by optical trap pulling experiment.光学陷阱牵引实验探测多体流体动力学相互作用。
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本文引用的文献

1
High-Resolution Optical Tweezers Combined with Multicolor Single-Molecule Microscopy.高分辨率光镊与多色单分子显微镜联用
Methods Mol Biol. 2022;2478:141-240. doi: 10.1007/978-1-0716-2229-2_8.
2
Hydrodynamically Controlled Self-Organization in Mixtures of Active and Passive Colloids.活性与被动胶体混合物中的流体动力学控制自组织
Small. 2022 May;18(21):e2107023. doi: 10.1002/smll.202107023. Epub 2022 Mar 19.
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Optical tweezers in single-molecule biophysics.单分子生物物理学中的光镊
Nat Rev Methods Primers. 2021;1. doi: 10.1038/s43586-021-00021-6. Epub 2021 Mar 25.
4
Hydrodynamic Elastocapillary Morphing of Hair Bundles.水动力弹性发束变形。
Phys Rev Lett. 2020 Dec 18;125(25):254503. doi: 10.1103/PhysRevLett.125.254503.
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Hydrodynamic interaction facilitates the unsteady transport of two neighboring vesicles.水动力相互作用促进了两个相邻囊泡的非稳态输运。
J Chem Phys. 2019 Sep 7;151(9):094108. doi: 10.1063/1.5113880.
6
Chemotaxis in a binary mixture of active and passive particles.活性与惰性粒子二元混合物中的趋化性。
J Chem Phys. 2019 Jun 7;150(21):214901. doi: 10.1063/1.5080543.
7
Hydrodynamic self-assembly of active colloids: chiral spinners and dynamic crystals.活性胶体的流体动力学自组装:手性纺缍和动态晶体。
Soft Matter. 2019 Feb 13;15(7):1508-1521. doi: 10.1039/c8sm02352b.
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Rational design and dynamics of self-propelled colloidal bead chains: from rotators to flagella.自推进胶体颗粒链的合理设计和动力学:从转子到鞭毛。
Sci Rep. 2017 Dec 1;7(1):16758. doi: 10.1038/s41598-017-16731-5.
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Hydrodynamic interactions in dense active suspensions: From polar order to dynamical clusters.密集活性悬浮液中的流体动力学相互作用:从极性有序到动态簇
Phys Rev E. 2017 Aug;96(2-1):020603. doi: 10.1103/PhysRevE.96.020603. Epub 2017 Aug 29.
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Short-time dynamics of monomers and dimers in quasi-two-dimensional colloidal mixtures.
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