聚乙二醇构象在混合层中的作用:从蛋白质冠底物到空间稳定避免蛋白质吸附

Joan Comenge
{"title":"聚乙二醇构象在混合层中的作用:从蛋白质冠底物到空间稳定避免蛋白质吸附","authors":"Joan Comenge","doi":"10.14293/S2199-1006.1.SOR-MATSCI.A0Z6OM.V1","DOIUrl":null,"url":null,"abstract":"Although nanoparticles have been traditionally modified with a single ligand layer, mixture of ligands might help to combine different functionalities and to further engineer the NP surface. A detailed study of the competition between an alkanethiol (11-mercaptoundecanoic acid) and SH-PEG for the surface of AuNPs and the resultant behaviors of this model nanoconjugate is presented here. As a result, the physicochemical properties of these conjugates can be progressively tuned by controlling the composition and especially the conformation of the mixed monolayer. This has implications in the physiological stability. The controlled changes on the SH-PEG conformation rather than its concentration induces a change in the stabilization mechanism from electrostatic repulsion to steric hindrance, which changes the biological fate of NPs. Importantly, the adsorption of proteins on the conjugates can be tailored by tuning the composition and conformation of the mixed layer.","PeriodicalId":91169,"journal":{"name":"ScienceOpen research","volume":"156 1","pages":"1-10"},"PeriodicalIF":0.0000,"publicationDate":"2015-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":"{\"title\":\"The role of PEG conformation in mixed layers: from protein corona substrate to steric stabilization avoiding protein adsorption\",\"authors\":\"Joan Comenge\",\"doi\":\"10.14293/S2199-1006.1.SOR-MATSCI.A0Z6OM.V1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Although nanoparticles have been traditionally modified with a single ligand layer, mixture of ligands might help to combine different functionalities and to further engineer the NP surface. A detailed study of the competition between an alkanethiol (11-mercaptoundecanoic acid) and SH-PEG for the surface of AuNPs and the resultant behaviors of this model nanoconjugate is presented here. As a result, the physicochemical properties of these conjugates can be progressively tuned by controlling the composition and especially the conformation of the mixed monolayer. This has implications in the physiological stability. The controlled changes on the SH-PEG conformation rather than its concentration induces a change in the stabilization mechanism from electrostatic repulsion to steric hindrance, which changes the biological fate of NPs. Importantly, the adsorption of proteins on the conjugates can be tailored by tuning the composition and conformation of the mixed layer.\",\"PeriodicalId\":91169,\"journal\":{\"name\":\"ScienceOpen research\",\"volume\":\"156 1\",\"pages\":\"1-10\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-03-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ScienceOpen research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14293/S2199-1006.1.SOR-MATSCI.A0Z6OM.V1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ScienceOpen research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14293/S2199-1006.1.SOR-MATSCI.A0Z6OM.V1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

摘要

虽然纳米颗粒传统上是用单一配体层修饰的,但配体的混合物可能有助于组合不同的功能,并进一步设计NP表面。本文详细研究了烷硫醇(11-巯基十四酸)和SH-PEG之间对AuNPs表面的竞争以及由此产生的模型纳米共轭物的行为。因此,这些共轭物的物理化学性质可以通过控制混合单层的组成,特别是构象来逐步调整。这与生理稳定性有关。SH-PEG构象(而非其浓度)的可控变化导致稳定机制由静电斥力向位阻转变,从而改变了NPs的生物学命运。重要的是,可以通过调整混合层的组成和构象来调整蛋白质在共轭物上的吸附。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
The role of PEG conformation in mixed layers: from protein corona substrate to steric stabilization avoiding protein adsorption
Although nanoparticles have been traditionally modified with a single ligand layer, mixture of ligands might help to combine different functionalities and to further engineer the NP surface. A detailed study of the competition between an alkanethiol (11-mercaptoundecanoic acid) and SH-PEG for the surface of AuNPs and the resultant behaviors of this model nanoconjugate is presented here. As a result, the physicochemical properties of these conjugates can be progressively tuned by controlling the composition and especially the conformation of the mixed monolayer. This has implications in the physiological stability. The controlled changes on the SH-PEG conformation rather than its concentration induces a change in the stabilization mechanism from electrostatic repulsion to steric hindrance, which changes the biological fate of NPs. Importantly, the adsorption of proteins on the conjugates can be tailored by tuning the composition and conformation of the mixed layer.
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
自引率
0.00%
发文量
0
审稿时长
1 weeks
期刊最新文献
A review: CRISPR/Cas12-mediated genome editing in fungal cells: advancements, mechanisms, and future directions in plant-fungal pathology Psychosocial risks in the working environment – approaches to formative risk assessment Technological, legal, and sociological summary of biometric technology usage Policy learning from influenza and the preparedness of the public health sector: 2006/2007 influenza season in Latvia Mpemba Effect- the Effect of Time
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1