Salatto Daniel, Huang Zhixing, Benziger Peter Todd, Carrillo Jan-Michael Y, Bajaj Yashasvi, Gauer Aiden, Tsapatsaris Leonidas, Sumpter Bobby G, Li Ruipeng, Takenaka Mikihito, Yin Wei, Thanassi David G, Endoh Maya, Koga Tadanori
Department of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York11794-2275, United States.
Department of Microbiology and Immunology, Stony Brook University, Stony Brook, New York11794-5222, United States.
ACS Appl Mater Interfaces. 2023 Jan 18;15(2):3420-3432. doi: 10.1021/acsami.2c18121. Epub 2023 Jan 4.
Here, we report synergistic nanostructured surfaces combining bactericidal and bacteria-releasing properties. A polystyrene--poly(methyl methacrylate) (PS--PMMA) diblock copolymer is used to fabricate vertically oriented cylindrical PS structures ("PS nanopillars") on silicon substrates. The results demonstrate that the PS nanopillars (with a height of about 10 nm, size of about 50 nm, and spacing of about 70 nm) exhibit highly effective bactericidal and bacteria-releasing properties ("dual properties") against for at least 36 h of immersion in an solution. Interestingly, the PS nanopillars coated with a thin layer (≈3 nm thick) of titanium oxide (TiO) ("TiO nanopillars") show much improved dual properties against (a Gram-negative bacterium) compared to the PS nanopillars. Moreover, the dual properties emerge against (a Gram-positive bacterium). To understand the mechanisms underlying the multifaceted property of the nanopillars, coarse-grained molecular dynamics (MD) simulations of a lipid bilayer (as a simplified model for ) in contact with a substrate containing hexagonally packed hydrophilic nanopillars were performed. The MD results demonstrate that when the bacterium-substrate interaction is strong, the lipid heads adsorb onto the nanopillar surfaces, conforming the shape of a lipid bilayer to the structure/curvature of nanopillars and generating high stress concentrations within the membrane (i.e., the driving force for rupture) at the edge of the nanopillars. Membrane rupture begins with the formation of pores between nanopillars (i.e., bactericidal activity) and ultimately leads to the membrane withdrawal from the nanopillar surface (i.e., bacteria-releasing activity). In the case of Gram-positive bacteria, the adhesion area to the pillar surface is limited due to the inherent stiffness of the bacteria, creating higher stress concentrations within a bacterial cell wall. The present study provides insight into the mechanism underlying the "adhesion-mediated" multifaceted property of nanosurfaces, which is crucial for the development of next-generation antibacterial surface coatings for relevant medical applications.
在此,我们报道了兼具杀菌和细菌释放特性的协同纳米结构表面。聚苯乙烯 - 聚(甲基丙烯酸甲酯)(PS - PMMA)二嵌段共聚物用于在硅基板上制备垂直取向的圆柱形PS结构(“PS纳米柱”)。结果表明,PS纳米柱(高度约10nm,尺寸约50nm,间距约70nm)在浸入细菌溶液中至少36小时后,对细菌表现出高效的杀菌和细菌释放特性(“双重特性”)。有趣的是,与PS纳米柱相比,涂覆有薄层(约3nm厚)氧化钛(TiO)的PS纳米柱(“TiO纳米柱”)对大肠杆菌(一种革兰氏阴性菌)表现出大大改善的双重特性。此外,对金黄色葡萄球菌(一种革兰氏阳性菌)也呈现出双重特性。为了理解纳米柱多方面特性背后的机制,我们进行了粗粒度分子动力学(MD)模拟,将脂质双层(作为细菌的简化模型)与含有六边形排列亲水性纳米柱的基板接触。MD结果表明,当细菌与基板的相互作用很强时,脂质头部吸附到纳米柱表面,使脂质双层的形状与纳米柱的结构/曲率相符,并在纳米柱边缘的膜内产生高应力浓度(即破裂的驱动力)。膜破裂始于纳米柱之间形成孔隙(即杀菌活性),最终导致膜从纳米柱表面退缩(即细菌释放活性)。对于革兰氏阳性菌,由于细菌固有的硬度,其与柱表面的粘附面积有限,从而在细菌细胞壁内产生更高的应力浓度。本研究深入了解了纳米表面“粘附介导”多方面特性背后的机制,这对于开发用于相关医学应用的下一代抗菌表面涂层至关重要。