Building a binding community - Capacity and capability for affinity and kinetic analysis of molecular interactions.
Building a binding community - Capacity and capability for affinity and kinetic analysis of molecular interactions.
批准号:
MR/X013227/1
负责人:
Iain Manfield
金额:
$33.88万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2022
资助国家:
英国
项目状态:
已结题
起止时间:
2022 至 --
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The cells of our bodies contain many thousands of different molecules. Like the parts making a machine, these have to work together correctly for us to be healthy. Some molecules work with each other, assembled into long-lasting machines to do their jobs. Other molecules work as short signals which are quickly switched off. Sometimes these normal processes go wrong, through cancer or genetic mutation. The machine we want to buy will help us understand what has gone wrong with these molecules. It will also help us find molecules we might develop into drugs to get things working correctly again. All other organisms including those causing disease such as bacteria and viruses also contain molecules making machines and sending signals. Understanding how these molecules work can help us target diseases. We can also use the machine to develop tests to detect diseases more quickly. Like Lego versus Duplo - the shape, size and stickiness of those different molecules affects which ones are able to interact with each other. However, the comparison with children's toys is only useful as a starting point for thinking about how molecules stick to each other, or don't. It turns out there's a whole set of words to describe Lego bricks. The bumps on each block are called "studs" which fit into holes in another brick. The shape and size of "studs" is important for the blocks sticking to each other. If molecules worked like Lego, then our job would be easy. It's child's play understanding how Lego works. Biology though uses different kinds of studs to stick molecules together. Molecules are more like a mixture of Lego studs, Duplo and Velcro - different shapes of sticky bits. It becomes very difficult to predict which molecules will interact with each and how tightly, or which won't interact. Sometimes we just need to mix things and see what happens. The machine we want to buy will do this mixing, telling us how strongly molecules will stick to each other and which molecules can't stick to each other. It will do this for hundreds of molecules, running overnight. With lots of information, we can better design more experiments to help us understand how molecules work and what happens when things go wrong, causing diseases.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1016/j.celrep.2023.113184
发表时间:
2023-09-29
期刊:
CELL REPORTS
影响因子:
8.8
作者:
[Martin,Heather L., Turner,Amy L., Tomlinson,Darren C.]
通讯作者:
Tomlinson,Darren C.
国内基金
海外基金
登录
查看更多内容
BRD4通过结合TEAD1调控β细胞增殖分化的机制研究
-
批准号:82370801
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:李峰
-
依托单位:
PCBP1和PCBP2调控cGAS的相变和酶活的机制研究
-
批准号:32370928
-
项目类别:面上项目
-
资助金额:50.00万元
-
批准年份:2023
-
负责人:孙钦秒
-
依托单位:
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
-
批准号:32170319
-
项目类别:面上项目
-
资助金额:58.00万元
-
批准年份:2021
-
负责人:董春海
-
依托单位:
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
-
批准号:--
-
项目类别:--
-
资助金额:58万元
-
批准年份:2021
-
负责人:董春海
-
依托单位:
用于对微管动态结构实时定量分析的荧光探针
-
批准号:32070708
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:谢松波
-
依托单位:
微管结合蛋白WDR62调节有丝分裂纺锤体极微管负端动态性的功能及机制
-
批准号:32070705
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:姜恺
-
依托单位:
Kinesin-8调控微管动态及减数分裂I期同源染色体分离的分子机制
-
批准号:32070707
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:符传孩
-
依托单位:
TOX3-WDR5信号轴靶向ABCG2促进结肠癌细胞干性维持及化疗和靶向治疗耐药的功能、分子机制和临床意义
-
批准号:82072711
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2020
-
负责人:郭微
-
依托单位:
ENKD1在纺锤体定向中的作用及分子机制
-
批准号:32000490
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:孙爽
-
依托单位:
果蝇纤毛细胞中特化细胞骨架的结构及其建立的分子基础解析
-
批准号:32070704
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:梁鑫
-
依托单位: