High Sensitivity Cryoprobe Equipment for the NMR Facility of the Department of Biochemistry University of Cambridge
High Sensitivity Cryoprobe Equipment for the NMR Facility of the Department of Biochemistry University of Cambridge
批准号:
BB/E013228/1
负责人:
Daniel Nietlispach
金额:
$30.85万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2007
资助国家:
英国
项目状态:
已结题
起止时间:
2007 至 --
中文摘要
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英文摘要
NMR spectroscopy has emerged as a powerful tool to study the structure and mobility of biomacromolecules such as proteins and nucleic acids in their natural environment in solution. A particularly powerful feature of NMR is that interactions of molecules can be studied at an atomic level that allows to differentiate e.g. functional from structural regions in a protein and permit to characterize which residues are involved in a interaction at molecular level. Strengths and timescales of such interactions can be determined which reveal information about the underlying physical mechanisms behind such interactions. Unfortunately, NMR spectroscopy is a relatively insensitive method so that the majority of currently available studies have been limited to smaller proteins < 20 kDa. More recently novel techniques and improved spectrometer hardware have led to a dramatic increase in the basic sensitivity so that the study of larger biomacromolecules has become possible. One such significant advance has been the introduction of the so-called cryoprobe that improves the sensitivity of NMR experiments between two and five-fold. This dramatically higher sensitivity can be used to good advantage, to study larger proteins and their complexes with other proteins or DNA/RNA typically not accessible with conventional equipment, to investigate less abundant or aggregating proteins, or to reduce the time required to perform a particular NMR experiment, thus increasing the capacity of the spectrometer. Our Departmental NMR facility forms a collaborative research environment that serves a wide range of users from the Departments of Biochemistry and Chemistry that work on a multitude of structural projects. Many of these projects involve work with large proteins, or multi-protein complexes or have to be conducted at low protein concentrations so that this work would dramatically benefit from the availability of such cryoprobe equipment. In this application we are requesting funds to install cryoprobes on two out of our four facility machines to be able to pursue our proposed research projects. Some of our outlined projects are extremely demanding and high sensitivity NMR equipment is a pre-requisite for their feasibility. Here are some selected examples of biological and clinical importance from our research plan. Our areas of work cover structural studies of molecules and complexes involved in many aspects of cell-signalling and their implications in cell motility and cancer and the study of cancer susceptibility syndrome proteins involved e.g. in Fanconi Anaemia, a disease that leads to progressive bone marrow failure. Further projects study different aspects of misfolding of proteins such as can be found in plaque in brain tissue of patients that have the debilitating diseases of Alzheimer's or Parkinson's. The study of chromatin, central to the control of gene expression, it's interactions with DNA and many proteins is another major significant research area. Structural studies on intact ribosomes, the cellular centers where protein synthesis occurs, are relatively new and particularly challenging to perform due to the very low concentrations and limited lifetimes of the synthesized nascent protein attached to the ribosome. As a final example we mention the structural study of membrane proteins. These proteins account for ca. 30% of all encoded proteins and control a vast range of biological functions such as respiration, signalling and transport at a molecular level. As they are water insoluble structural information is hardly available. NMR can study such proteins in a detergent solubilized form but the large size of such complexes requires the highest NMR sensitivity available.
期刊论文(9)
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会议论文
1H, 13C and 15N resonance assignments for Binder of Arl2, BART.
Arl2、BART 的 Binder 的 1H、13C 和 15N 共振分配。
DOI:
10.1007/s12104-008-9135-3
发表时间:
2009
期刊:
Biomolecular NMR assignments
影响因子:
0.9
作者:
[Bailey LK]
通讯作者:
Bailey LK
DOI:
10.1007/s12104-008-9115-7
发表时间:
2008-12-01
期刊:
BIOMOLECULAR NMR ASSIGNMENTS
影响因子:
0.9
作者:
[Bryn Fenwick, R., Prasannan, Sunil, Mott, Helen R.]
通讯作者:
Mott, Helen R.
A dynamic view of GPCR-G protein complexes: insight into partial agonism and G protein selectivity
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批准号:BB/W020718/1
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项目类别:Research Grant
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资助金额:$70.49万
-
财政年份:2022
-
负责人:Daniel Nietlispach
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依托单位:
Understanding the functional activation of G protein-coupled receptors (GPCRs) in the context of their lipid bilayer environment
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批准号:BB/S015892/1
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项目类别:Research Grant
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资助金额:$61.25万
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财政年份:2019
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负责人:Daniel Nietlispach
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依托单位:
Solution NMR spectroscopy studies of an adrenergic receptor b1AR
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批准号:BB/K01983X/1
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项目类别:Research Grant
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资助金额:$57.78万
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财政年份:2013
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负责人:Daniel Nietlispach
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依托单位:
Structure determination of the 7-helix transmembrane protein receptor pSRII by solution NMR
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批准号:BB/G011915/1
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项目类别:Research Grant
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资助金额:$47.97万
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财政年份:2009
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负责人:Daniel Nietlispach
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依托单位:
海外基金