Tan Sue Woon, Gooran Negin, Lim Hye Min, Yoon Bo Kyeong, Jackman Joshua A
School of Chemical Engineering and Translational Nanobioscience Research Center, Sungkyunkwan University, Suwon 16419, Republic of Korea.
School of Healthcare and Biomedical Engineering, Chonnam National University, Yeosu 59626, Republic of Korea.
Nanomaterials (Basel). 2023 Feb 26;13(5):874. doi: 10.3390/nano13050874.
In light of regulatory considerations, there are ongoing efforts to identify Triton X-100 (TX-100) detergent alternatives for use in the biological manufacturing industry to mitigate membrane-enveloped pathogen contamination. Until now, the efficacy of antimicrobial detergent candidates to replace TX-100 has been tested regarding pathogen inhibition in endpoint biological assays or probing lipid membrane disruption in real-time biophysical testing platforms. The latter approach has proven especially useful to test compound potency and mechanism of action, however, existing analytical approaches have been limited to studying indirect effects of lipid membrane disruption such as membrane morphological changes. A direct readout of lipid membrane disruption by TX-100 detergent alternatives would be more practical to obtain biologically relevant information to guide compound discovery and optimization. Herein, we report the use of electrochemical impedance spectroscopy (EIS) to investigate how TX-100 and selected replacement candidates-Simulsol SL 11W (Simulsol) and cetyltrimethyl ammonium bromide (CTAB)-affect the ionic permeability of tethered bilayer lipid membrane (tBLM) platforms. The EIS results revealed that all three detergents exhibited dose-dependent effects mainly above their respective critical micelle concentration (CMC) values while displaying distinct membrane-disruptive behaviors. TX-100 caused irreversible membrane disruption leading to complete solubilization, whereas Simulsol caused reversible membrane disruption and CTAB induced irreversible, partial membrane defect formation. These findings establish that the EIS technique is useful for screening the membrane-disruptive behaviors of TX-100 detergent alternatives with multiplex formatting possibilities, rapid response, and quantitative readouts relevant to antimicrobial functions.
鉴于监管方面的考虑,目前正在努力寻找用于生物制造业的Triton X-100(TX-100)洗涤剂替代品,以减轻膜包膜病原体污染。到目前为止,抗菌洗涤剂候选物替代TX-100的功效已在终点生物学试验中针对病原体抑制进行了测试,或在实时生物物理测试平台中探测脂质膜破坏情况。后一种方法已被证明对于测试化合物的效力和作用机制特别有用,然而,现有的分析方法仅限于研究脂质膜破坏的间接影响,如膜形态变化。通过TX-100洗涤剂替代品直接读出脂质膜破坏情况,对于获取生物学相关信息以指导化合物发现和优化将更为实用。在此,我们报告使用电化学阻抗谱(EIS)来研究TX-100以及选定的替代候选物——Simulsol SL 11W(Simulsol)和十六烷基三甲基溴化铵(CTAB)——如何影响拴系双层脂质膜(tBLM)平台的离子渗透性。EIS结果显示,所有三种洗涤剂主要在各自的临界胶束浓度(CMC)值以上表现出剂量依赖性效应,同时呈现出不同的膜破坏行为。TX-100导致不可逆的膜破坏,最终完全溶解,而Simulsol导致可逆的膜破坏,CTAB诱导不可逆的部分膜缺陷形成。这些发现表明,EIS技术可用于筛选TX-100洗涤剂替代品的膜破坏行为,具有多重格式化可能性、快速响应以及与抗菌功能相关的定量读数。