米替福新影响革兰氏阳性菌的小分子转运

IF 4.2 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Marea J. Blake, Eleanor F. Page, Madeline E. Smith and Tessa R. Calhoun
{"title":"米替福新影响革兰氏阳性菌的小分子转运","authors":"Marea J. Blake, Eleanor F. Page, Madeline E. Smith and Tessa R. Calhoun","doi":"10.1039/D4CB00106K","DOIUrl":null,"url":null,"abstract":"<p >Miltefosine (MLT) is an alkylphosphocholine with clinical success as an anticancer and antiparasitic drug. Although the mechanism of action of MLT is highly debated, the interaction of MLT with the membrane, specifically lipid rafts of eukaryotes, is well-documented. Recent reports suggest MLT impacts the functional membrane microdomains in bacteria – regions of the membrane structurally and functionally similar to lipid rafts. There have been conflicting reports, however, as to whether MLT impacts the overall fluidity of cellular plasma membranes. Here, we apply steady-state fluorescence techniques, generalized polarization of laurdan and anisotropy of diphenylhexatriene, to discern how MLT impacts the global ordering and lipid packing of <em>Staphylococcus aureus</em> membranes. Additionally, we investigate how the transport of a range of small molecules is impacted by MLT for <em>S. aureus</em> and <em>Bacillus subtilis</em> by employing time-resolved second harmonic scattering. Overall, we observe MLT does not have an influence on the overall ordering and packing of <em>S. aureus</em> membranes. Additionally, we show that the transport of small molecules across the membrane can be significantly altered by MLT – although this is not the case for all molecules studied. The results presented here illustrate the potential use of MLT as an adjuvant to assist in the delivery of drug molecules in bacteria.</p>","PeriodicalId":40691,"journal":{"name":"RSC Chemical Biology","volume":" 10","pages":" 981-988"},"PeriodicalIF":4.2000,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/cb/d4cb00106k?page=search","citationCount":"0","resultStr":"{\"title\":\"Miltefosine impacts small molecule transport in Gram-positive bacteria†\",\"authors\":\"Marea J. Blake, Eleanor F. Page, Madeline E. Smith and Tessa R. Calhoun\",\"doi\":\"10.1039/D4CB00106K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Miltefosine (MLT) is an alkylphosphocholine with clinical success as an anticancer and antiparasitic drug. Although the mechanism of action of MLT is highly debated, the interaction of MLT with the membrane, specifically lipid rafts of eukaryotes, is well-documented. Recent reports suggest MLT impacts the functional membrane microdomains in bacteria – regions of the membrane structurally and functionally similar to lipid rafts. There have been conflicting reports, however, as to whether MLT impacts the overall fluidity of cellular plasma membranes. Here, we apply steady-state fluorescence techniques, generalized polarization of laurdan and anisotropy of diphenylhexatriene, to discern how MLT impacts the global ordering and lipid packing of <em>Staphylococcus aureus</em> membranes. Additionally, we investigate how the transport of a range of small molecules is impacted by MLT for <em>S. aureus</em> and <em>Bacillus subtilis</em> by employing time-resolved second harmonic scattering. Overall, we observe MLT does not have an influence on the overall ordering and packing of <em>S. aureus</em> membranes. Additionally, we show that the transport of small molecules across the membrane can be significantly altered by MLT – although this is not the case for all molecules studied. The results presented here illustrate the potential use of MLT as an adjuvant to assist in the delivery of drug molecules in bacteria.</p>\",\"PeriodicalId\":40691,\"journal\":{\"name\":\"RSC Chemical Biology\",\"volume\":\" 10\",\"pages\":\" 981-988\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/cb/d4cb00106k?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Chemical Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/cb/d4cb00106k\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Chemical Biology","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/cb/d4cb00106k","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

米替福新(MLT)是一种烷基磷胆碱,作为抗癌和抗寄生虫药物在临床上取得了成功。尽管对 MLT 的作用机制存在很大争议,但 MLT 与膜(特别是真核生物的脂筏)的相互作用已得到充分证实。最近的报告表明,MLT 会影响细菌的功能膜微域--在结构上和功能上类似于脂质筏的膜区域。然而,关于 MLT 是否会影响细胞质膜的整体流动性,一直以来都有相互矛盾的报道。在这里,我们应用稳态荧光技术、月桂丹的广义偏振和二苯基己三烯的各向异性,来揭示 MLT 如何影响金黄色葡萄球菌膜的整体有序性和脂质堆积。此外,我们还利用时间分辨二次谐波散射研究了金黄色葡萄球菌和枯草杆菌的 MLT 如何影响一系列小分子的运输。总体而言,我们观察到 MLT 对金黄色葡萄球菌膜的整体有序和堆积没有影响。此外,我们还发现小分子在膜上的传输会受到 MLT 的显著影响,尽管并非所有研究的分子都是如此。本文介绍的结果说明了 MLT 作为辅助剂用于协助细菌中药物分子输送的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Miltefosine impacts small molecule transport in Gram-positive bacteria†

Miltefosine impacts small molecule transport in Gram-positive bacteria†

Miltefosine impacts small molecule transport in Gram-positive bacteria†

Miltefosine (MLT) is an alkylphosphocholine with clinical success as an anticancer and antiparasitic drug. Although the mechanism of action of MLT is highly debated, the interaction of MLT with the membrane, specifically lipid rafts of eukaryotes, is well-documented. Recent reports suggest MLT impacts the functional membrane microdomains in bacteria – regions of the membrane structurally and functionally similar to lipid rafts. There have been conflicting reports, however, as to whether MLT impacts the overall fluidity of cellular plasma membranes. Here, we apply steady-state fluorescence techniques, generalized polarization of laurdan and anisotropy of diphenylhexatriene, to discern how MLT impacts the global ordering and lipid packing of Staphylococcus aureus membranes. Additionally, we investigate how the transport of a range of small molecules is impacted by MLT for S. aureus and Bacillus subtilis by employing time-resolved second harmonic scattering. Overall, we observe MLT does not have an influence on the overall ordering and packing of S. aureus membranes. Additionally, we show that the transport of small molecules across the membrane can be significantly altered by MLT – although this is not the case for all molecules studied. The results presented here illustrate the potential use of MLT as an adjuvant to assist in the delivery of drug molecules in bacteria.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.10
自引率
0.00%
发文量
128
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信