课题基金 / 基金详情

Optical Fluorescence Micro and Nanoscopy to determine and quantify functional molecular interactions and dynamics across time and length scales

Optical Fluorescence Micro and Nanoscopy to determine and quantify functional molecular interactions and dynamics across time and length scales
光学荧光显微和纳米显微镜可确定和量化跨时间和长度尺度的功能性分子相互作用和动力学
批准号:
BB/V019791/1
负责人:
Jorge Bernardino De La Serna
金额:
$66.8万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2021
资助国家:
英国
项目状态:
已结题
起止时间:
2021 至 --

项目摘要

项目成果

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中文摘要
翻译
光学显微镜是现代生物科学和医学研究的基石,它允许从单个分子到生物体的各个尺度上对过程进行检查。在这里,我们建议购买一个最近发布的高端系统,使我们能够执行最先进的“超分辨率”显微镜,并有可能在分子水平上执行时间分辨成像。这将使我们能够以无与伦比的空间和时间分辨率研究细胞中的事件。至关重要的是,这些系统将允许bbsrc资助的研究人员和其他研究人员推动研究项目,了解分子驱动的基本机制,其相互作用和动力学,从单个细胞水平到细胞的集体功能组装。该显微镜将成为帝国理工学院“成像和光学显微镜设施”(FILM)的一部分,并向学院的所有成员以及当地,国家和国际合作者开放。
英文摘要
Light microscopy forms a bedrock of modern research in bioscience and medicine, allowing processes to be examined across scales from individual molecules up to living organisms. Here we propose to acquire a high-end recently released system to enable us to perform state-of-the-art "super resolution" microscopy, with the possibility to perform time-resolved imaging at molecular level. This will allow us to study events in cells with unparalleled spatial and temporal resolution. Critically, these systems will permit BBSRC-funded and other researchers to drive research projects understanding the fundamental mechanisms driven by molecules, its interactions and dynamics at the single cellular level up to collective functional assemblies of cells. The microscope will be part of Imperial's "Facility for Imaging and Light microscopy" (FILM) and accessible to all members of College, as well as local, national and international collaborators.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1021/acs.langmuir.2c03349
发表时间: 2023-03-28
期刊: LANGMUIR
影响因子: 3.9
作者: [Liekkinen, Juho, Olzynska, Agnieszka, Cwiklik, Lukasz, de la Serna, Jorge Bernardino, Javanainen, Matti, Vattulainen, Ilpo]
通讯作者: Vattulainen, Ilpo
Excess filaggrin in keratinocytes is removed by extracellular vesicles to prevent premature death and this mechanism can be hijacked by Staphylococcus aureus in a TLR2-dependent fashion
角质形成细胞中多余的丝聚蛋白被细胞外囊泡去除,以防止过早死亡,并且这种机制可以被金黄色葡萄球菌以 TLR2 依赖性方式劫持
DOI: 10.21203/rs.3.rs-2085299/v1
发表时间: 2022
期刊:
影响因子: --
作者: [Hovhannisyan L]
通讯作者: Hovhannisyan L
Surfactant Proteins SP-B and SP-C in Pulmonary Surfactant Monolayers: Physical Properties Controlled by Specific Protein-Lipid Interactions
肺表面活性剂单层中的表面活性剂蛋白 SP-B 和 SP-C:由特定蛋白质-脂质相互作用控制的物理性质
DOI: 10.1101/2022.12.12.520108
发表时间: 2022
期刊:
影响因子: --
作者: [Liekkinen J]
通讯作者: Liekkinen J
DOI: 10.1101/2021.03.02.433589
发表时间: 2021
期刊:
影响因子: --
作者: [Bernabé-Rubio M]
通讯作者: Bernabé-Rubio M
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