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氧化石墨烯纳米片通过破坏细胞骨架来抑制细胞迁移。

Graphene Oxide Nanosheets Retard Cellular Migration via Disruption of Actin Cytoskeleton.

机构信息

School for Radiological and Interdisciplinary Sciences (RAD-X), Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, 215123, China.

Computational Biology Center, IBM Thomas J. Watson Research Center, Yorktown Heights, New York, NY, 10598, USA.

出版信息

Small. 2017 Jan;13(3). doi: 10.1002/smll.201602133. Epub 2016 Oct 20.


DOI:10.1002/smll.201602133
PMID:27762498
Abstract

Graphene and graphene-based nanomaterials are broadly used for various biomedical applications due to their unique physiochemical properties. However, how graphene-based nanomaterials interact with biological systems has not been thoroughly studied. This study shows that graphene oxide (GO) nanosheets retard A549 lung carcinoma cell migration through nanosheet-mediated disruption of intracellular actin filaments. After GO nanosheets treatment, A549 cells display slower migration and the structure of the intracellular actin filaments is dramatically changed. It is found that GO nanosheets are capable of absorbing large amount of actin and changing the secondary structures of actin monomers. Large-scale all-atom molecular dynamics simulations further reveal the interactions between GO nanosheets and actin filaments at molecular details. GO nanosheets can insert into the interstrand gap of actin tetramer (helical repeating unit of actin filament) and cause the separation of the tetramer which eventually leads to the disruption of actin filaments. These findings offer a novel mechanism of GO nanosheet induced biophysical responses and provide more insights into their potential for biomedical applications.

摘要

由于其独特的物理化学性质,石墨烯和基于石墨烯的纳米材料被广泛用于各种生物医学应用。然而,基于石墨烯的纳米材料如何与生物系统相互作用还没有得到彻底的研究。本研究表明,氧化石墨烯(GO)纳米片通过纳米片介导的细胞内肌动蛋白丝的破坏来抑制 A549 肺癌细胞的迁移。在 GO 纳米片处理后,A549 细胞的迁移速度变慢,细胞内肌动蛋白丝的结构发生显著变化。研究发现,GO 纳米片能够吸收大量的肌动蛋白并改变肌动蛋白单体的二级结构。大规模全原子分子动力学模拟进一步揭示了 GO 纳米片与肌动蛋白丝在分子细节上的相互作用。GO 纳米片可以插入肌动蛋白四聚体的链间间隙(肌动蛋白丝的螺旋重复单元),并导致四聚体的分离,最终导致肌动蛋白丝的破坏。这些发现提供了 GO 纳米片诱导生物物理响应的新机制,并为它们在生物医学应用中的潜力提供了更深入的了解。

相似文献

[1]
Graphene Oxide Nanosheets Retard Cellular Migration via Disruption of Actin Cytoskeleton.

Small. 2016-10-20

[2]
Microfluidic investigation of the effect of graphene oxide on mechanical properties of cell and actin cytoskeleton networks: experimental and theoretical approaches.

Sci Rep. 2021-8-10

[3]
The effects of graphene oxide nanosheets localized on F-actin filaments on cell-cycle alterations.

Biomaterials. 2012-11-22

[4]
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[5]
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[6]
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Biomaterials. 2014-9-8

[7]
Protein corona-mediated mitigation of cytotoxicity of graphene oxide.

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[8]
Hydration patterns of graphene-based nanomaterials (GBNMs) play a major role in the stability of a helical protein: a molecular dynamics simulation study.

Langmuir. 2013-11-4

[9]
Direct Observation, Molecular Structure, and Location of Oxidation Debris on Graphene Oxide Nanosheets.

Environ Sci Technol. 2016-8-3

[10]
Graphene Oxide Induced Perturbation to Plasma Membrane and Cytoskeletal Meshwork Sensitize Cancer Cells to Chemotherapeutic Agents.

ACS Nano. 2017-2-20

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[3]
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[4]
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[5]
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[6]
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[7]
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