Kallmyer Nathaniel E, Agarwal Sparsh, Eeg Danielle, Khor Rachel, Roby Nathan, Vela Ramirez Alma, Hillier Andrew C, Reuel Nigel F
Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
ACS Appl Mater Interfaces. 2023 Sep 27;15(38):44621-44630. doi: 10.1021/acsami.3c06592. Epub 2023 Sep 18.
Membrane-active molecules are of great importance to drug delivery and antimicrobials applications. While the ability to prototype new membrane-active molecules has improved greatly with the advent of automated chemistries and rapid biomolecule expression techniques, testing methods are still limited by throughput, cost, and modularity. Existing methods suffer from feasibility constraints of working with pathogenic living cells and by intrinsic limitations of model systems. Herein, we demonstrate an abiotic sensor that uses semiconducting single-walled carbon nanotubes (SWCNTs) as near-infrared fluorescent transducers to report membrane interactions. This sensor is composed of SWCNTs aqueously suspended in lipid, creating a cylindrical, bilayer corona; these SWCNT probes are very sensitive to solvent access (changes in permittivity) and thus report morphological changes to the lipid corona by modulation of fluorescent signals, where binding and disruption are reported as brightening and attenuation, respectively. This mechanism is first demonstrated with chemical and physical membrane-disruptive agents, including ethanol and sodium dodecyl sulfate, and application of electrical pulses. Known cell-penetrating and antimicrobial peptides are then used to demonstrate how the dynamic response of these sensors can be deconvoluted to evaluate different parallel mechanisms of interaction. Last, SWCNTs functionalized in several different bacterial lipopolysaccharides (, , and ) are used to evaluate a panel of known membrane-disrupting antimicrobials to demonstrate that drug selectivity can be assessed by suspension of SWCNTs with different membrane materials.
膜活性分子在药物递送和抗菌应用中具有重要意义。随着自动化化学合成技术和快速生物分子表达技术的出现,新型膜活性分子的原型设计能力有了很大提高,但测试方法仍受通量、成本和模块化的限制。现有方法受到处理致病性活细胞的可行性限制以及模型系统的固有局限性。在此,我们展示了一种非生物传感器,它使用半导体单壁碳纳米管(SWCNT)作为近红外荧光换能器来报告膜相互作用。该传感器由悬浮在脂质中的SWCNT水溶液组成,形成圆柱形的双层冠层;这些SWCNT探针对溶剂可及性(介电常数变化)非常敏感,因此通过荧光信号的调制来报告脂质冠层的形态变化,其中结合和破坏分别表现为荧光增强和减弱。首先用化学和物理膜破坏剂(包括乙醇和十二烷基硫酸钠)以及电脉冲来证明这种机制。然后使用已知的细胞穿透肽和抗菌肽来证明如何对这些传感器的动态响应进行解卷积,以评估不同的平行相互作用机制。最后,用几种不同细菌脂多糖(、和)功能化的SWCNT来评估一组已知的膜破坏抗菌剂,以证明可以通过将SWCNT与不同膜材料悬浮来评估药物选择性。