A curated, publically-accessible database of protein nanoscale organisation
蛋白质纳米级组织的精选、可公开访问的数据库
基本信息
- 批准号:BB/X018644/1
- 负责人:
- 金额:$ 72.75万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2023
- 资助国家:英国
- 起止时间:2023 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
Current descriptions of cellular systems are incomplete. They can be characterised at the genomic, transcriptomic and proteomic level, but there is a final level: How those proteins are organised in 3D space. This information is now accessible to scientists because of the advent of super-resolution microscopy, especially single-molecule imaging (SMLM) which allows the positions of biomolecules to be mapped with nanometer precision. Well-curated, publically-accessible databases have been transformative across biology. Well established databases, such as GenBank are ubiquitously used, but the data they contain are relatively simplistic. Somewhat more complex data sets include protein structure databases, for example PDB and the associated predicted structures from DeepMind's AlphaFold2. This application builds on initial Alan Turing Institute, EPSRC and BBSRC investment with the aim to become a national and global resource for the storage, sharing, curating and processing of SMLM data. Once established, we will lay the foundations for a new field of -omics, nano-omics: the study of protein nanoscale organisation.Ultimatly, the resource will be a database where users can store, share and disseminate their SMLM data, benefitting the public engagement with science, aiding collaboration and helping meet data sharing mandates of funders and publishers. A community management structure will ensure the database follows best practice for research ethics and scientific excellence. The database will also feature advanced data analysis tools running in the cloud allwoing users to extract biologically relecvant information from uploaded datasets. This aids in bringing advanced statistical analysis to those without means and helping to democratize advanced imaging. Finally, we will conduct primary research into the meta-analysis of the uploaded data and initiate a new field of nano-omics - the study of the diversity of protein nanoscale organisation between proteins, cells and organisms.
目前对细胞系统的描述还不完整。它们可以在基因组、转录组学和蛋白质组学水平上进行表征,但还有一个最终的水平:这些蛋白质是如何在3D空间中组织的。由于超分辨率显微镜,特别是单分子成像(SMLM)的出现,科学家们现在可以获得这些信息,这使得生物分子的位置可以以纳米精度绘制。精心策划、可公开访问的数据库已经改变了整个生物学。建立良好的数据库,如基因库,被广泛使用,但它们包含的数据相对简单。更复杂的数据集包括蛋白质结构数据库,例如PDB和来自DeepMind的AlphaFold2的相关预测结构。该应用程序建立在艾伦图灵研究所、EPSRC和BBSRC的初始投资基础上,旨在成为存储、共享、管理和处理SMLM数据的国家和全球资源。一旦建立,我们将为组学的一个新领域奠定基础,纳米组学:蛋白质纳米级组织的研究。最终,该资源将成为一个数据库,用户可以在其中存储、共享和传播他们的SMLM数据,使公众参与科学,协助合作,并帮助满足资助者和出版商的数据共享要求。社区管理结构将确保数据库遵循研究伦理和科学卓越的最佳实践。该数据库还将以运行在云端的高级数据分析工具为特色,允许用户从上传的数据集中提取生物学相关信息。这有助于为那些没有手段的人带来先进的统计分析,并有助于先进成像的民主化。最后,我们将对上传的数据进行meta分析,并启动纳米组学的一个新领域——蛋白质、细胞和生物体之间的蛋白质纳米级组织多样性的研究。
项目成果
期刊论文数量(0)
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会议论文数量(0)
专利数量(0)
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Dylan Owen其他文献
Clustering of the Mechanosensitive Ion Channels of Large and Small Conductance MscL and MscS - a FRET-Flim Study
- DOI:
10.1016/j.bpj.2011.11.674 - 发表时间:
2012-01-31 - 期刊:
- 影响因子:
- 作者:
Charles G. Cranfield;Evelyne Deplazes;Alex MacMillan;Dylan Owen;Takeshi Nomura;Maryrose Constantine;Ben Corry;Boris Martinac - 通讯作者:
Boris Martinac
Molecular Mechanism of T Cell Signaling
- DOI:
10.1016/j.bpj.2011.11.128 - 发表时间:
2012-01-31 - 期刊:
- 影响因子:
- 作者:
Katharina Gaus;David Williamson;Jeremie Rossy;Dylan Owen;Astrid Magenau - 通讯作者:
Astrid Magenau
Dylan Owen的其他文献
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{{ truncateString('Dylan Owen', 18)}}的其他基金
Bayesian and machine-learning-based analysis of high-volume super-resolution microscopy data for molecular-level cell phenotyping
基于贝叶斯和机器学习的大容量超分辨率显微镜数据分析,用于分子水平细胞表型分析
- 批准号:
BB/R007365/1 - 财政年份:2018
- 资助金额:
$ 72.75万 - 项目类别:
Research Grant
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