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胆固醇层的熵斥力会对抗生物附着。

Entropic repulsion of cholesterol-containing layers counteracts bioadhesion.

机构信息

Institute of Biofunctional Polymer Materials, Leibniz Institute of Polymer Research Dresden, Dresden, Germany.

Institute of Theory of Polymers, Leibniz Institute of Polymer Research Dresden, Dresden, Germany.

出版信息

Nature. 2023 Jun;618(7966):733-739. doi: 10.1038/s41586-023-06033-4. Epub 2023 Jun 21.

Abstract

Control of adhesion is a striking feature of living matter that is of particular interest regarding technological translation. We discovered that entropic repulsion caused by interfacial orientational fluctuations of cholesterol layers restricts protein adsorption and bacterial adhesion. Moreover, we found that intrinsically adhesive wax ester layers become similarly antibioadhesive when containing small quantities (under 10 wt%) of cholesterol. Wetting, adsorption and adhesion experiments, as well as atomistic simulations, showed that repulsive characteristics depend on the specific molecular structure of cholesterol that encodes a finely balanced fluctuating reorientation at the interface of unconstrained supramolecular assemblies: layers of cholesterol analogues differing only in minute molecular variations showed markedly different interfacial mobility and no antiadhesive effects. Also, orientationally fixed cholesterol layers did not resist bioadhesion. Our insights provide a conceptually new physicochemical perspective on biointerfaces and may guide future material design in regulation of adhesion.

摘要

控制黏附是生命物质的一个显著特征,这对于技术转化尤其重要。我们发现,胆固醇层界面取向波动引起的熵斥力限制了蛋白质吸附和细菌黏附。此外,我们发现当含有少量(低于 10wt%)胆固醇时,原本具有黏附性的蜡酯层也会变得同样具有抗生物黏附性。润湿、吸附和黏附实验以及原子模拟表明,排斥特性取决于胆固醇的特定分子结构,这种结构在无约束的超分子组装的界面处编码了一种精细平衡的波动重定向:仅在微小分子变化上有所不同的胆固醇类似物层显示出明显不同的界面迁移率,并且没有抗黏附作用。此外,取向固定的胆固醇层不能抵抗生物黏附。我们的研究结果为生物界面提供了一个全新的物理化学视角,并可能为未来控制黏附的材料设计提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a3/10284698/2a5c1793af0e/41586_2023_6033_Fig1_HTML.jpg

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