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本文引用的文献

1
Using nanotechniques to explore microbial surfaces.运用纳米技术探索微生物表面。
Nat Rev Microbiol. 2004 Jun;2(6):451-60. doi: 10.1038/nrmicro905.
2
Atomic force microscopy study of living diatoms in ambient conditions.环境条件下活硅藻的原子力显微镜研究。
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Aggregation of yeast cells: direct measurement of discrete lectin-carbohydrate interactions.酵母细胞聚集:离散凝集素-碳水化合物相互作用的直接测量
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Molecular nanosprings in spider capture-silk threads.蜘蛛捕捉丝中的分子纳米弹簧。
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Single-molecule folding.单分子折叠
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Heterogeneity in bacterial surface polysaccharides, probed on a single-molecule basis.基于单分子水平对细菌表面多糖异质性的探究。
Biomacromolecules. 2002 Jul-Aug;3(4):661-7. doi: 10.1021/bm015648y.
7
Characterization of the adhesive mucilages secreted by live diatom cells using atomic force microscopy.使用原子力显微镜对活硅藻细胞分泌的粘性粘液进行表征。
Protist. 2002 Mar;153(1):25-38. doi: 10.1078/1434-4610-00080.
8
Segmented nanofibers of spider dragline silk: atomic force microscopy and single-molecule force spectroscopy.蜘蛛拖牵丝的分段纳米纤维:原子力显微镜和单分子力谱学
Proc Natl Acad Sci U S A. 2002 Apr 30;99 Suppl 2(Suppl 2):6460-5. doi: 10.1073/pnas.082526499. Epub 2002 Apr 16.
9
Bone indentation recovery time correlates with bond reforming time.骨压痕恢复时间与骨痂重塑时间相关。
Nature. 2001 Dec 13;414(6865):773-6. doi: 10.1038/414773a.
10
Mechanical unfolding of single filamin A (ABP-280) molecules detected by atomic force microscopy.通过原子力显微镜检测单根细丝蛋白A(ABP - 280)分子的机械展开。
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来自活硅藻的单根粘性纳米纤维具有模块化蛋白质的特征指纹。

Single adhesive nanofibers from a live diatom have the signature fingerprint of modular proteins.

作者信息

Dugdale T M, Dagastine R, Chiovitti A, Mulvaney P, Wetherbee R

机构信息

School of Botany, School of Chemical and Biomolecular Engineering, University of Melbourne, Melbourne, Australia.

出版信息

Biophys J. 2005 Dec;89(6):4252-60. doi: 10.1529/biophysj.105.062489. Epub 2005 Sep 16.

DOI:10.1529/biophysj.105.062489
PMID:16169972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1366990/
Abstract

The adhesive and mechanical properties of a cell-substratum adhesive secreted by live diatom cells were examined in situ using atomic force microscopy. The resulting force curves have a regular saw-tooth pattern, the characteristic fingerprint of modular proteins, and when bridged between tip and surface can repeatedly be stretched and relaxed resulting in precisely overlaying saw-tooth curves (up to approximately 600 successive cycles). The average rupture force of the peaks is 0.794 +/- 0.007 (mean +/- SE) nN at a loading rate of 0.8 microm/s and the average persistence length is 0.026 +/- <0.001 (mean +/- SE) nm (fit using the worm-like chain model). We propose that we are pulling on single adhesive nanofibers, each a cohesive unit composed of a set number of modular proteins aligned in register. Furthermore, we can observe and differentiate when up to three adhesive nanofibers are pulled based upon multimodal distributions of force and persistence length. The high force required for bond rupture, high extensibility (approximately 1.2 microm), and the accurate and rapid refolding upon relaxation, together provide strong and flexible properties ideally suited for the cell-substratum adhesion of this fouling diatom and allow us to understand the mechanism responsible for the strength of adhesion.

摘要

利用原子力显微镜原位检测了活硅藻细胞分泌的细胞-基质黏附物的黏附及力学性能。所得力曲线呈现出规则的锯齿状图案,这是模块化蛋白质的特征指纹,当在探针与表面之间架桥时,其可反复拉伸和松弛,从而产生精确重叠的锯齿状曲线(多达约600个连续循环)。在加载速率为0.8微米/秒时,峰值的平均断裂力为0.794±0.007(平均值±标准误差)纳牛,平均持续长度为0.026±<0.001(平均值±标准误差)纳米(使用蠕虫状链模型拟合)。我们提出,我们正在拉动单个黏附性纳米纤维,每个纳米纤维都是由一定数量对齐排列的模块化蛋白质组成的内聚单元。此外,基于力和持续长度的多峰分布,当拉动多达三根黏附性纳米纤维时,我们能够进行观察和区分。键断裂所需的高力、高延伸性(约1.2微米)以及松弛时准确快速的重新折叠,共同提供了强大且灵活的性能,非常适合这种污损硅藻的细胞-基质黏附,并使我们能够理解负责黏附强度的机制。