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本文引用的文献

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Asymmetric Lipid Vesicles: Techniques, Applications, and Future Perspectives as an Innovative Drug Delivery System.不对称脂质囊泡:作为一种创新药物递送系统的技术、应用及未来展望
Pharmaceuticals (Basel). 2023 May 23;16(6):777. doi: 10.3390/ph16060777.
2
Characterizing the Interactions of Cell-Membrane-Disrupting Peptides with Lipid-Functionalized Single-Walled Carbon Nanotubes.表征细胞膜破坏肽与脂质功能化单壁碳纳米管的相互作用。
ACS Appl Mater Interfaces. 2023 May 24;15(20):24084-24096. doi: 10.1021/acsami.3c01217. Epub 2023 May 15.
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Characterizing the Structure and Interactions of Model Lipid Membranes Using Electrophysiology.利用电生理学表征模型脂质膜的结构与相互作用
Membranes (Basel). 2021 Apr 27;11(5):319. doi: 10.3390/membranes11050319.
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Inexpensive Near-Infrared Fluorimeters: Enabling Translation of nIR-Based Assays to the Field.廉价近红外荧光计:推动基于近红外的检测方法在现场的应用。
Anal Chem. 2021 Mar 23;93(11):4800-4808. doi: 10.1021/acs.analchem.0c03732. Epub 2021 Mar 11.
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Atomic force microscopy to elucidate how peptides disrupt membranes.原子力显微镜阐明肽如何破坏膜。
Biochim Biophys Acta Biomembr. 2021 Jan 1;1863(1):183447. doi: 10.1016/j.bbamem.2020.183447. Epub 2020 Aug 21.
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ElectroPen: An ultra-low-cost, electricity-free, portable electroporator.电转笔:一种超低成本、无电源、便携式电穿孔仪。
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Measuring the Accessible Surface Area within the Nanoparticle Corona Using Molecular Probe Adsorption.使用分子探针吸附测量纳米颗粒冠层内的可及表面积。
Nano Lett. 2019 Nov 13;19(11):7712-7724. doi: 10.1021/acs.nanolett.9b02647. Epub 2019 Nov 4.
8
New and old tools to evaluate new antimicrobial peptides.评估新型抗菌肽的新旧工具。
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9
Rapid prototyping of proteins: Mail order gene fragments to assayable proteins within 24 hours.蛋白质的快速原型制作:在 24 小时内将订购的基因片段邮寄到可检测的蛋白质。
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10
An optical nanoreporter of endolysosomal lipid accumulation reveals enduring effects of diet on hepatic macrophages in vivo.一种内溶酶体脂质积累的光学纳米报告器揭示了饮食对体内肝巨噬细胞的持久影响。
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脂质功能化单壁碳纳米管作为筛选细胞壁破坏剂的探针

Lipid-Functionalized Single-Walled Carbon Nanotubes as Probes for Screening Cell Wall Disruptors.

作者信息

Kallmyer Nathaniel E, Agarwal Sparsh, Eeg Danielle, Khor Rachel, Roby Nathan, Vela Ramirez Alma, Hillier Andrew C, Reuel Nigel F

机构信息

Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.

出版信息

ACS Appl Mater Interfaces. 2023 Sep 27;15(38):44621-44630. doi: 10.1021/acsami.3c06592. Epub 2023 Sep 18.

DOI:10.1021/acsami.3c06592
PMID:37721709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11806933/
Abstract

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.

摘要

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。