Creating a Synthetic Platform for Understanding and Exploiting Glycoconjugates
Creating a Synthetic Platform for Understanding and Exploiting Glycoconjugates
批准号:
EP/E000614/1
负责人:
Benjamin Davis
金额:
$82.3万
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
碳水化合物在生物学中的重要性的证据呈指数增长。与其他生物分子(脂质、蛋白质、核苷)不同,在用于理解和利用这种生物学的相应糖缀合物探针的构建中需要大量的专业知识:例如,迄今为止还没有用于构建所有糖苷键的自动寡糖合成仪。像六糖结构这样简单的东西的可能排列延伸到大于1.05 x 1012种可能的组合。这种复杂程度强调了糖缀合物的合成必须由功能设计指导,并且不能简单地通过随机合成所有可能的组合来实现。在糖科学领域存在着许多令人震惊和具有挑战性的高风险问题,该平台将使我们能够解决这些问题。风险很高,复杂性的挑战很大(部分原因是生物学中通常缺乏对糖缀合物合成的直接遗传控制),但潜在的回报是巨大的。
英文摘要
The evidence for the importance of carbohydrates in biology is increasing exponentially. Unlike other biomolecules (lipids, proteins, nucleosides) significant expertise is needed in the construction of corresponding glycoconjugate probes used to understand and exploit this biology: for example, no automated oligosaccharide synthesizer to date exists for the construction of all the glycoside linkages. The possible permutations for something as simple as the hexasaccharide structures stretch to greater than 1.05 x 1012 possible combinations. This level of complexity highlights that synthesis of glycoconjugates must be guided by functional design, and cannot simply be achieved through random synthesis of all possible combinations. There are a number of startling and challenging high-risk problems that exist in the field of glycoscience that the Platform would allow us to tackle. The risk is high, the challenges of complexity great (due, in part, to the typical lack of direct genetic control of glycoconjugate synthesis within biology) but the potential rewards are tremendous.
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DOI:
10.1038/nchembio.539
发表时间:
2011-04
期刊:
NATURE CHEMICAL BIOLOGY
影响因子:
14.8
作者:
[Backus, Keriann M., Boshoff, Helena L., Barry, Conor S., Boutureira, Omar, Patel, Mitul K., D'Hooge, Francois, Lee, Seung Seo, Via, Laura E., Tahlan, Kapil, Barry, Clifton E., III, Davis, Benjamin G.]
通讯作者:
Davis, Benjamin G.
Direct Biocatalytic Conversion of Carbon Dioxide: Towards a Formic Acid Economy
二氧化碳的直接生物催化转化:迈向甲酸经济
DOI:
--
发表时间:
2007
期刊:
in preparation
影响因子:
--
作者:
[A Celik]
通讯作者:
A Celik
Creating new Tools for a Formic Acid Economy: Cloning & Structure of Novel Dehydrogenases
为甲酸经济创造新工具:克隆
DOI:
--
发表时间:
2007
期刊:
in preparation
影响因子:
--
作者:
[A Celik]
通讯作者:
A Celik
Multimeric microparticles of iron oxide (mMPIO) for dual modality molecular imaging with CT & MRI
用于 CT 双模态分子成像的氧化铁多聚微粒 (mMPIO)
DOI:
--
发表时间:
2014
期刊:
EUROPEAN HEART JOURNAL
影响因子:
39.3
作者:
[Aljabali A. A. A.]
通讯作者:
Aljabali A. A. A.
Microparticles bearing RGD peptide promote integrin avß3-dependent platelet adhesion in isolated, pressurized cerebral artery
携带 RGD 肽的微粒促进分离的加压脑动脉中整合素 avä3 依赖性血小板粘附
DOI:
--
发表时间:
2013
期刊:
FASEB JOURNAL
影响因子:
4.8
作者:
[Bagi Zsolt]
通讯作者:
Bagi Zsolt
共 7 条
ISOBIOTICS: Isotopic Labeling of Biotherapeutics
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-
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Exploring and Driving Cooperative International Strategies in Sustainable Chiral Pool Natural Product Synthesis
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Rosalind Franklin Institute - Next Generation Chemistry
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Understanding a Mutant that Disregulates Trehalose 6-Phosphate Action in Plants
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A High-throughput discovery facility for the Rosalind Franklin Institute
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Understanding and Exploiting Tunicamycin (Bio)Synthesis to Enable Novel Antibiotics and Inhibitors
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财政年份:2012
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负责人:Benjamin Davis
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依托单位:
Engineering stable calibration standards for biomedical research
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批准号:EP/I500200/1
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项目类别:Research Grant
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资助金额:$12.95万
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财政年份:2011
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依托单位:
The CHELL : A Bottom-Up approach to in vitro and in silico Minimal Life-like Constructs
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资助金额:$73.14万
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财政年份:2009
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负责人:Benjamin Davis
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依托单位:
Dissecting the mechanism by which glycosyltransferases calalyse mannosyl transfer
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-
项目类别:Research Grant
-
资助金额:$49.38万
-
财政年份:2007
-
负责人:Benjamin Davis
-
依托单位:
海外基金