Physics of Life - Noise, Information and Evolution in Protein Binding
Physics of Life - Noise, Information and Evolution in Protein Binding
批准号:
EP/N031431/1
负责人:
Tom McLeish
金额:
$179.95万
依托单位:
依托单位国家:
英国
项目类别:
Fellowship
财政年份:
2017
资助国家:
英国
项目状态:
已结题
起止时间:
2017 至 --
中文摘要
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英文摘要
How does order emerge from chaos? As if the 'miracle of life' in all its complexity were not enough to astonish us, the molecular story of how the information and energy flows occur within living cells and organisms tells an even stranger tale. For at the dimensions of life's molecular building blocks - the long protein molecules that fold up perfectly into functional forms, the even longer DNA that codes for the structure of its organisms, the cell membranes that marshal biochemical traffic between the cell and its surroundings - all these are subject to continual, rapid random fluctuation. The thermal jostling of every component seems, at first, to fight against the appearance of the order and structure that are the emergent signs of life. However, recent interdisciplinary collaborations between physicists and biologists have begun to discover just how deeply life has evolved to work with the noisy fluctuations rather than to fight them.This project will devote 5 years of focussed research to explore in detail three fundamental ways in which randomness and noise are recruited in biology, bringing the experience of the proposed Fellow, two post-doctoral research fellows and an extensive community of collaborators, to bear. The first example is right at the heart of information-processing in cells. 'Allostery' is the effect by which a protein molecule binds to another molecule (either a smaller species, or a giant molecule like DNA) if and only if a second 'signalling' molecule is also bound to it, at a different site. The presence of the signalling molecule is felt 'at a distance' at the other binding site. We will develop theoretical and computational tools to explore how the background of thermal fluctuations can be used to carry the signal, and learn from biology about the physics of fluctuating elastic matter.The second example continues the theme of protein-binding, but now to other proteins. The outstanding properties of spider and silkworm silk are even more outstanding when we discover how the fibres are made in nature. Somehow the molecular 'stickiness' of silk proteins is just enough to trigger their assembly into fibres when just the right flow conditions apply (at the spinneret). Working closely with experimental colleagues, we will develop theories of assembly in flow to help find out what makes silk, and its processing, so remarkable.A third stream of work takes the idea of random motion but now at the higher level of evolution itself. The search for the protein structures that deliver the binding properties of signalling and silk takes place in an unimaginably vast space of possibilities coded by the organism's genome. Random jumps in this space, like the random motions of the proteins themselves, somehow serve to find solutions, rather than frustrate them. We have an exciting opportunity to use the methods of 'noisy physics' at the molecular level to explore the physics of evolution itself, asking the question. 'How does nature search for, and find solutions?'. Completing the circle of the project, we will construct theories for the evolution of the sticky proteins themselves.
期刊论文(10)
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DOI:
10.1021/acs.jpclett.2c00704
发表时间:
2022-06-09
期刊:
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
影响因子:
5.7
作者:
[Dresser, Lara, Graham, Sarah P., Miller, Lisa M., Schaefer, Charley, Conteduca, Donato, Johnson, Steven, Leake, Mark C., Quinn, Steven D.]
通讯作者:
Quinn, Steven D.
Membraneless organelles formed by liquid-liquid phase separation increase bacterial fitness.
液-液相分离形成的无膜细胞器提高细菌适应性
DOI:
10.1126/sciadv.abh2929
发表时间:
2021-10-22
期刊:
Science advances
影响因子:
13.6
作者:
[Jin X, Lee JE, Schaefer C, Luo X, Wollman AJM, Payne-Dwyer AL, Tian T, Zhang X, Chen X, Li Y, McLeish TCB, Leake MC, Bai F]
通讯作者:
Bai F
DOI:
10.3389/fnmol.2022.962526
发表时间:
2022
期刊:
FRONTIERS IN MOLECULAR NEUROSCIENCE
影响因子:
4.8
作者:
[Connor, Jack P. P., Quinn, Steven D. D., Schaefer, Charley]
通讯作者:
Schaefer, Charley
Membraneless organelles formed by liquid-liquid phase separation increase bacterial fitness
液-液相分离形成的无膜细胞器提高细菌适应性
DOI:
10.1101/2021.06.24.449778
发表时间:
2021
期刊:
影响因子:
--
作者:
[Jin X]
通讯作者:
Jin X
Fluorescence Recovery After Photobleaching (FRAP) to Study Dynamics of the Structural Maintenance of Chromosome (SMC) Complex in Live Escherichia coli Bacteria.
光漂白后的荧光恢复 (FRAP) 用于研究活大肠杆菌中染色体 (SMC) 复合物结构维持的动态。
DOI:
10.1007/978-1-0716-2221-6_4
发表时间:
2022
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
[Badrinarayanan A]
通讯作者:
Badrinarayanan A
Physics of Life - Noise, Information and Evolution in Protein Binding
-
批准号:EP/N031431/2
-
项目类别:Fellowship
-
资助金额:$154.46万
-
财政年份:2018
-
负责人:Tom McLeish
-
依托单位:
Physics of Life Network 2 (PoLNet2)
-
批准号:EP/P006639/1
-
项目类别:Research Grant
-
资助金额:$32.37万
-
财政年份:2017
-
负责人:Tom McLeish
-
依托单位:
2010 Grant balance: Durham University
-
批准号:EP/J021547/1
-
项目类别:Research Grant
-
资助金额:$10.52万
-
财政年份:2011
-
负责人:Tom McLeish
-
依托单位:
New Multiscale Tools for Protein Physics: Thermal Protein Dynamics in Signalling and Allostery.
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批准号:EP/H051759/1
-
项目类别:Research Grant
-
资助金额:$109.77万
-
财政年份:2010
-
负责人:Tom McLeish
-
依托单位:
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