Velic Amar, Hasan Jafar, Li Zhiyong, Yarlagadda Prasad K D V
School of Mechanical, Medical and Process Engineering, Queensland University of Technology, Brisbane, Queensland, Australia; Centre for Biomedical Technologies, Queensland University of Technology, Brisbane, Queensland, Australia.
School of Mechanical, Medical and Process Engineering, Queensland University of Technology, Brisbane, Queensland, Australia; Centre for Biomedical Technologies, Queensland University of Technology, Brisbane, Queensland, Australia.
Biophys J. 2021 Jan 19;120(2):217-231. doi: 10.1016/j.bpj.2020.12.003. Epub 2020 Dec 15.
Nanopatterned surfaces are believed to kill bacteria through physical deformation, a mechanism that has immense potential against biochemical resistance. Because of its elusive nature, this mechanism is mostly understood through biophysical modeling. Problematically, accurate descriptions of the contact mechanics and various boundary conditions involved in the bacteria-nanopattern interaction remain to be seen. This may underpin conflicting predictions, found throughout the literature, regarding two important aspects of the mechanism-that is, its critical action site and relationship with geometry. Herein, a robust computational analysis of bacteria-nanopattern interaction is performed using a three-dimensional finite element modeling that incorporates relevant continuum mechanical properties, multilayered envelope structure, and adhesion interaction conditions. The model is applied to more accurately study the elusory mechanism and its enhancement via nanopattern geometry. Additionally, micrographs of bacteria adhered on a nanopatterned cicada wing are examined to further inform and verify the major modeling predictions. Together, the results indicate that nanopatterned surfaces do not kill bacteria predominantly by rupture in between protruding pillars as previously thought. Instead, nondevelopable deformation about pillar tips is more likely to create a critical site at the pillar apex, which delivers significant in-plane strains and may locally rupture and penetrate the cell. The computational analysis also demonstrates that envelope deformation is increased by adhesion to nanopatterns with smaller pillar radii and spacing. These results further progress understanding of the mechanism of nanopatterned surfaces and help guide their design for enhanced bactericidal efficiency.
纳米图案化表面被认为是通过物理变形来杀灭细菌的,这一机制在对抗生物化学抗性方面具有巨大潜力。由于其难以捉摸的性质,这种机制主要是通过生物物理建模来理解的。问题在于,对于细菌与纳米图案相互作用中涉及的接触力学和各种边界条件的准确描述仍有待观察。这可能是文献中关于该机制的两个重要方面——即其关键作用位点及其与几何形状的关系——存在相互矛盾预测的原因。在此,使用三维有限元建模对细菌与纳米图案的相互作用进行了稳健的计算分析,该建模纳入了相关的连续介质力学特性、多层包膜结构和粘附相互作用条件。该模型用于更准确地研究这种难以捉摸的机制及其通过纳米图案几何形状的增强作用。此外,还检查了附着在纳米图案化蝉翼上的细菌的显微照片,以进一步为主要建模预测提供信息并进行验证。综合来看,结果表明纳米图案化表面并非如先前认为的那样主要通过突出柱体之间的破裂来杀灭细菌。相反,柱体尖端的不可展变形更有可能在柱体顶端形成一个关键位点,该位点会产生显著的面内应变,并可能局部破裂并穿透细胞。计算分析还表明,通过与具有较小柱体半径和间距的纳米图案的粘附,包膜变形会增加。这些结果进一步推动了对纳米图案化表面机制的理解,并有助于指导其设计以提高杀菌效率。