Conformational states of membrane proteins: Technology development for bioscience
Conformational states of membrane proteins: Technology development for bioscience
批准号:
BB/H017402/1
负责人:
Samantha Miller
金额:
$29.35万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2010
资助国家:
英国
项目状态:
已结题
起止时间:
2010 至 --
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Although life requires water, life must be able to control the flow of water. As an example, if a person (70% water) jumps into a swimming pool they do not dissolve like a sugar cube. This is because we have a barrier between the swimming pool water and the water inside our cells. This barrier is the membrane or lipid bilayer, it is made of oily compounds. The bilayer is essential it keeps important things in and poisonous things out. All organisms have these bilayers. On their own bilayers would simply block all transport, thus we could not take up nutrients nor could we get rid of waste. Proteins embedded in this membrane are thus needed to act as gate keepers to control movements of ions, nutrients, waste and proteins across the lipid bilayer. These proteins are also the telephone connections between one cell and another. The nerve impulse in humans transmits trigger release of a transmitter (small chemical) from the neuron. The transmitter interacts with another cell by promoting some change in the cell, each cell uses membrane proteins as part of this process. Membrane proteins that control ions movement across the bilayer are called ion channels. They must, like a tap, be able to fully closed to stop leaks but they must also open when required. Many diseases are caused by membrane proteins not working properly. If we are to treat these diseases we need to understand how membrane proteins work. Protein crystallography has transformed our understanding of proteins. It allows us to see every atom in the structure and understand a great deal about the function of the protein. This scientific approach has led to the development of many new drugs. However, this technique can only see one state of the protein at a time. We propose to develop a new approach that will allow us to see in detail exactly how membrane proteins move between the open and closed states. We have chosen to study the pain receptors in humans and the osmotic stress survival proteins in bacteria. These are important systems with obvious medical benefits, treatment of pain and design of new antibiotics.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1016/j.bpj.2014.01.008
发表时间:
2014-02-18
期刊:
BIOPHYSICAL JOURNAL
影响因子:
3.4
作者:
[Ward, Richard, Pliotas, Christos, Branigan, Emma, Hacker, Christian, Rasmussen, Akiko, Hagelueken, Gregor, Booth, Ian R., Miller, Samantha, Lucocq, John, Naismith, James H., Schiemann, Olav]
通讯作者:
Schiemann, Olav
Quantification of free cysteines in membrane and soluble proteins using a fluorescent dye and thermal unfolding.
使用荧光染料和热展开对膜和可溶性蛋白质中的自由半胱氨酸进行定量。
DOI:
10.1038/nprot.2013.128
发表时间:
2013-11
期刊:
Nature protocols
影响因子:
14.8
作者:
[]
通讯作者:
DOI:
10.1038/nsmb.3120
发表时间:
2015-12
期刊:
Nature structural & molecular biology
影响因子:
16.8
作者:
[Pliotas C, Dahl AC, Rasmussen T, Mahendran KR, Smith TK, Marius P, Gault J, Banda T, Rasmussen A, Miller S, Robinson CV, Bayley H, Sansom MS, Booth IR, Naismith JH]
通讯作者:
Naismith JH
国内基金
海外基金
双原子分子高激发振转能级的精确研究
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批准号:10774105
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项目类别:面上项目
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资助金额:35.0万元
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批准年份:2007
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负责人:孙卫国
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依托单位: