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粘菌 Dictyostelium discoideum 的粘附策略——力谱研究。

Adhesion strategies of Dictyostelium discoideum- a force spectroscopy study.

机构信息

Max Planck Institute for Dynamics and Self-Organization, Am Faßberg 17, 37077 Göttingen, Germany.

出版信息

Nanoscale. 2018 Dec 21;10(47):22504-22519. doi: 10.1039/c8nr07107a. Epub 2018 Nov 27.

DOI:10.1039/c8nr07107a
PMID:30480299
Abstract

Biological adhesion is essential for all motile cells and generally limits locomotion to suitably functionalized substrates displaying a compatible surface chemistry. However, organisms that face vastly varying environmental challenges require a different strategy. The model organism Dictyostelium discoideum (D.d.), a slime mould dwelling in the soil, faces the challenge of overcoming variable chemistry by employing the fundamental forces of colloid science. To understand the origin of D.d. adhesion, we realized and modified a variety of conditions for the amoeba comprising the absence and presence of the specific adhesion protein Substrate Adhesion A (sadA), glycolytic degradation, ionic strength, surface hydrophobicity and strength of van der Waals interactions by generating tailored model substrates. By employing AFM-based single cell force spectroscopy we could show that experimental force curves upon retraction exhibit two regimes. The first part up to the critical adhesion force can be described in terms of a continuum model, while the second regime of the curve beyond the critical adhesion force is governed by stochastic unbinding of individual binding partners and bond clusters. We found that D.d. relies on adhesive interactions based on EDL-DLVO (Electrical Double Layer-Derjaguin-Landau-Verwey-Overbeek) forces and contributions from the glycocalix and specialized adhesion molecules like sadA. This versatile mechanism allows the cells to adhere to a large variety of natural surfaces under various conditions.

摘要

生物黏附对于所有的运动细胞都是必不可少的,通常限制运动细胞在适当功能化的底物上移动,这些底物表现出兼容的表面化学性质。然而,面临着巨大的环境挑战的生物体需要一种不同的策略。模式生物盘基网柄菌(D.d.),一种生活在土壤中的黏菌,通过利用胶体科学的基本力量来克服多变的化学环境。为了了解 D.d.黏附的起源,我们实现并修改了多种条件,包括不存在和存在特定黏附蛋白 Substrate Adhesion A(sadA)、糖酵解降解、离子强度、表面疏水性和范德华相互作用强度,生成了定制的模型底物。通过使用基于原子力显微镜的单细胞力谱学,我们可以表明,在回缩过程中,实验力曲线表现出两个区域。第一部分,直至临界黏附力,可以用连续体模型来描述,而曲线的第二部分,即超过临界黏附力的部分,由单个结合伙伴和键簇的随机解吸来控制。我们发现,D.d.依赖于基于 EDL-DLVO(双电层-德贾金-朗道-弗洛凯)力的黏附相互作用以及糖萼和专门的黏附分子(如 sadA)的贡献。这种多功能的机制允许细胞在各种条件下黏附到各种天然表面上。

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