Simulations for Synthetic Biology: Mapping Biological Switches
Simulations for Synthetic Biology: Mapping Biological Switches
批准号:
EP/G042659/1
负责人:
Mark Sansom
金额:
$0.35万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2009
资助国家:
英国
项目状态:
已结题
起止时间:
2009 至 --
中文摘要
我们的身体是由许多叫做细胞的小构件组成的。每个细胞都在不断地吸收营养,接收来自身体其他部位的信号,并输出废物和产物。这些重要的功能是由每个细胞内产生的大分子——蛋白质来完成的。细胞通过开启和关闭这些蛋白质来控制这些功能。我们不太了解蛋白质是如何在这些状态之间切换的。合成生物学和生物纳米技术领域的研究人员受到这种复杂性的启发,正试图设计和构建自己的分子来完成某些事情。他们还希望他们的合成分子能够在不同的状态之间转换。在这项研究中,我们计划研究被称为α -螺旋的部分蛋白质是如何通过中间的扭结来采用不同的结构的。这已经被其他研究人员研究过了,然而,我们计划通过计算地图来显示每个转换状态的位置,以及α -螺旋在两种状态之间移动的容易程度。到目前为止,这是不可能的,因为需要大量的快速计算机来运行所有必要的模拟。我们计划使用HPCx,英国的国家超级计算机之一,来运行这些模拟。我们还将研究改变每个α -螺旋周围的环境如何影响其转换能力。因此,我们的研究不仅将阐明蛋白质如何能够在状态之间切换,而且还将帮助其他研究人员设计和构建合成分子。
英文摘要
Our bodies are made up of many small building blocks called cells. Each cell is constantly drawing in nutrients, receive signals from elsewhere in the body and export waste and products. These vital functions are performed by large molecules, called proteins, that are made within each cell. The cell controls these functions by switching the proteins on and off. We do not understand very well how proteins are able to switch between these states. Researchers in the synthetic biology and bionanotechnology fields have been inspired by this complexity and are trying to design and build their own molecules that do certain things. They also want their synthetic molecules to be able to switch between different states. In this study we plan to investigate how parts of proteins, called alpha-helices, are able to adopt different structures by kinking in the middle. This has been looked at by other researchers, however, we plan to compute maps showing where each of the switched states is and how easily the alpha-helix can move between the two states. This has not been possible until now because a very large number of fast computers are required to run all the necessary simulations. We plan to use HPCx, one of the UK's national supercomputers, to run these simulations. We shall also study how changing the environment around each alpha-helix affects its ability to switch. Our study will therefore not only shed light on how proteins are able to switch between states but will also help other researchers design and build synthetic molecules.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/ncomms2858
发表时间:
2013
期刊:
Nature communications
影响因子:
16.6
作者:
[]
通讯作者:
DOI:
10.1021/jz4014079
发表时间:
2013-09-19
期刊:
The journal of physical chemistry letters
影响因子:
--
作者:
[Fowler PW, Beckstein O, Abad E, Sansom MS]
通讯作者:
Sansom MS
DOI:
10.1021/ct4005933
发表时间:
2013-11-12
期刊:
JOURNAL OF CHEMICAL THEORY AND COMPUTATION
影响因子:
5.5
作者:
[Fowler, Philip W., Abad, Enrique, Beckstein, Oliver, Sansom, Mark S. P.]
通讯作者:
Sansom, Mark S. P.
Hydrophobic Gating in Membrane Nanopores: Water at the Nanoscale
-
批准号:EP/R004722/1
-
项目类别:Research Grant
-
资助金额:$48.38万
-
财政年份:2017
-
负责人:Mark Sansom
-
依托单位:
Nano to Meso and Back Again: Capturing and Exploiting Dynamic Heterogeneities in Biological Membranes via Large Scale Simulations
-
批准号:BB/R00126X/1
-
项目类别:Research Grant
-
资助金额:$44.93万
-
财政年份:2017
-
负责人:Mark Sansom
-
依托单位:
Crowding and Complexity: Simulation Studies of Biologically Realistic Membrane Models
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批准号:BB/L002558/1
-
项目类别:Research Grant
-
资助金额:$41.45万
-
财政年份:2014
-
负责人:Mark Sansom
-
依托单位:
CCP-BioSim: Biomolecular simulation at the life sciences interface
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批准号:EP/J010421/1
-
项目类别:Research Grant
-
资助金额:$10.28万
-
财政年份:2012
-
负责人:Mark Sansom
-
依托单位:
MemProtMD: A resource for membrane proteins
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批准号:BB/I019855/1
-
项目类别:Research Grant
-
资助金额:$44.29万
-
财政年份:2011
-
负责人:Mark Sansom
-
依托单位:
OMSys: Towards a systems model of a bacterial outer membrane
-
批准号:BB/H000267/1
-
项目类别:Research Grant
-
资助金额:$42.3万
-
财政年份:2009
-
负责人:Mark Sansom
-
依托单位:
海外基金