Collaborative Research: CIBR: Incorporating Crystallography and Cryo-EM Tools in Foldit
合作研究:CIBR:在 Foldit 中结合晶体学和冷冻电镜工具
基本信息
- 批准号:2051305
- 负责人:
- 金额:$ 31.34万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-06-01 至 2025-05-31
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
The goal of structural biologists is to visualize biomolecules at atomic resolution, which is a critical step in understanding all aspects of biology, including diseases and their cures. The dominant experimental methods for structure determination, called Cryo-Electron Microscopy and X-Ray Crystallography, rely upon fitting the atoms from biological molecules into three-dimensional “maps”, seeking agreement with experimental data. This fitting process is laborious and difficult, but preliminary studies have shown that this task could be performed very effectively by citizen scientists playing the biochemistry computer game Foldit. As a premier citizen science computer game, Foldit has already been played by over 600,000 people since its inception. This project aims to improve the capabilities of Foldit to enable scientists and citizen scientists alike to accurately build biological structures of varying types and sizes. This capability could strongly improve science’s ability to understand the basis of many biological phenomena. In addition to these scientific benefits, this project benefits both science education and society as a whole. This new capability will enhance the variety and quality of educational options using Foldit, improving it as a major interface between the scientific community and society.There is an ongoing need for improvements for methods to solve crystal and cryo-EM structures. Foldit is a citizen science project in which users aid in many biochemistry problems, including model building and real space refinement in protein structure solving projects. Early tests suggest that these ventures produce high quality crystal and cryo-EM structures, but many improvements are needed to make Foldit a go-to option for structure solving problems. Recently, new versions of Foldit have been introduced that can be used by single scientists or lab groups, in addition to standard citizen science Foldit puzzles. These options will be leveraged to create a multi-scale modeling toolbox for structural biology problems. The additions proposed in this grant include integrating new crystallography refinement capabilities within Foldit, and adding new modes that allow much larger proteins to be handled in Foldit for cryo-EM. Together, these improvements will make Foldit a state-of-the-art structure solving suite for crystallography and cryo-EM. Significant updates in the results of the project can be found at https://www.fold.it.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
结构生物学家的目标是在原子分辨率下可视化生物分子,这是理解生物学各个方面(包括疾病及其治疗)的关键一步。结构测定的主要实验方法称为冷冻电子显微镜和 X 射线晶体学。依靠将生物分子中的原子拟合成三维“图”,寻求与实验数据的一致性。这个拟合过程既费力又困难,但初步研究表明,通过玩生物化学计算机的公民科学家可以非常有效地完成这项任务。游戏 Foldit。作为一款顶级的公民科学计算机游戏,Foldit 自推出以来已有超过 600,000 人玩过。该项目旨在提高 Foldit 的功能,使科学家和公民科学家能够准确地构建不同类型和大小的生物结构。这种能力可以极大地提高科学理解许多生物现象的基础的能力。除了这些科学益处之外,该项目还有益于科学教育和整个社会,这种新能力将提高教育选择的多样性和质量。 Foldit,将其改进为科学界和社会之间的主要界面。人们一直需要改进解决晶体和冷冻电镜结构的方法,Foldit 是一个公民科学项目,用户可以在其中帮助解决许多生物化学问题,包括模型。早期测试表明,这些企业可以生产高质量的晶体和冷冻电镜结构,但需要进行许多改进才能使 Foldit 成为解决结构问题的首选。折叠已经除了标准的公民科学 Foldit 谜题外,该项目还介绍了可供单个科学家或实验室小组使用的功能,这些选项将用于创建结构生物学问题的多尺度建模工具箱。本次拨款中提出的补充包括整合新的晶体学细化。 Foldit 中的功能,并添加新的模式,允许在 Foldit 中处理更大的蛋白质以进行冷冻电镜,这些改进将使 Foldit 成为晶体学和冷冻电镜的最先进的结构求解套件。该项目结果的重要更新可在 https://www.fold.it 上找到。该奖项反映了 NSF 的法定使命,并通过使用基金会的智力价值和更广泛的影响审查标准进行评估,被认为值得支持。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Scott Horowitz其他文献
Human esophageal microvascular endothelial cells respond to acidic pH stress by PI3K/AKT and p38 MAPK-regulated induction of Hsp70 and Hsp27.
人食管微血管内皮细胞通过 PI3K/AKT 和 p38 MAPK 调节的 Hsp70 和 Hsp27 诱导来响应酸性 pH 应激。
- DOI:
10.1152/ajpcell.00474.2005 - 发表时间:
2006-11-01 - 期刊:
- 影响因子:0
- 作者:
P. Rafiee;Monica Theriot;V. Nelson;J. Heidemann;Yasmin Kanaa;Scott Horowitz;Aaron Rogaczewski;Christopher P. Johnson;I. Ali;R. Shaker;D. Binion - 通讯作者:
D. Binion
Roles of Nucleic Acids in Protein Folding, Aggregation, and Disease.
核酸在蛋白质折叠、聚集和疾病中的作用。
- DOI:
10.1021/acschembio.3c00695 - 发表时间:
2024-03-13 - 期刊:
- 影响因子:4
- 作者:
Theodore J Litberg;Scott Horowitz - 通讯作者:
Scott Horowitz
Correction for Lee et al., RNA design rules from a massive open laboratory
Lee 等人的更正,来自大型开放实验室的 RNA 设计规则
- DOI:
- 发表时间:
2015 - 期刊:
- 影响因子:11.1
- 作者:
Noor Siddiqui;Scott Horowitz;B. Koepnick;Raoul Martin;Agnes Tymieniecki;Amanda A. Winburn;Seth Cooper;J. Flatten;D. Rogawski;N. Koropatkin;Tsinatkeab T. Hailu;Neha Jain;P. Koldewey;Logan S. Ahlstrom;Matthew R. Chapman;Andrew P. Sikkema;M. Skiba;F. Maloney;Felix R. M. Beinlich;Zoran Popovic;David Baker;Firas Khatib;James C. A. Bardwell;R. Joosten - 通讯作者:
R. Joosten
A New Role for RNA G-quadruplexes in Aging and Alzheimer’s Disease
RNA G 四链体在衰老和阿尔茨海默病中的新作用
- DOI:
10.1101/2023.10.02.560545 - 发表时间:
2023-10-02 - 期刊:
- 影响因子:0
- 作者:
Lena Kallweit;E. Hamlett;Hannah Saternos;A. Gilmore;Ann;Scott Horowitz - 通讯作者:
Scott Horowitz
Manipulating TDP43 Aggregation via RNA G-quadruplexes
通过 RNA G 四链体操纵 TDP43 聚集
- DOI:
10.1101/2024.04.30.591873 - 发表时间:
2024-04-30 - 期刊:
- 影响因子:0
- 作者:
Emily G. Oldani;Kevin M. Reynolds Caicedo;McKenna E. Spaeth Herda;Adam H. Sachs;Erich G. Chapman;Sunil Kumar;Daniel A. Linseman;Scott Horowitz - 通讯作者:
Scott Horowitz
Scott Horowitz的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
相似国自然基金
IGF-1R调控HIF-1α促进Th17细胞分化在甲状腺眼病发病中的机制研究
- 批准号:82301258
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
CTCFL调控IL-10抑制CD4+CTL旁观者激活促口腔鳞状细胞癌新辅助免疫治疗抵抗机制研究
- 批准号:82373325
- 批准年份:2023
- 资助金额:49 万元
- 项目类别:面上项目
RNA剪接因子PRPF31突变导致人视网膜色素变性的机制研究
- 批准号:82301216
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
血管内皮细胞通过E2F1/NF-kB/IL-6轴调控巨噬细胞活化在眼眶静脉畸形中的作用及机制研究
- 批准号:82301257
- 批准年份:2023
- 资助金额:30 万元
- 项目类别:青年科学基金项目
基于多元原子间相互作用的铝合金基体团簇调控与强化机制研究
- 批准号:52371115
- 批准年份:2023
- 资助金额:50 万元
- 项目类别:面上项目
相似海外基金
Collaborative Research: CIBR: Leaping the Specimen Digitization Gap: Connecting Novel Tools, Machine Learning and Public Participation to Label Digitization Efforts
合作研究:CIBR:跨越标本数字化差距:将新工具、机器学习和公众参与与标签数字化工作联系起来
- 批准号:
2027241 - 财政年份:2021
- 资助金额:
$ 31.34万 - 项目类别:
Standard Grant
Collaborative Research: CIBR: Leaping the Specimen Digitization Gap: Connecting Novel Tools, Machine Learning and Public Participation to Label Digitization Efforts
合作研究:CIBR:跨越标本数字化差距:将新工具、机器学习和公众参与与标签数字化工作联系起来
- 批准号:
2027234 - 财政年份:2021
- 资助金额:
$ 31.34万 - 项目类别:
Standard Grant
Collaborative Research: CIBR: Incorporating Crystallography and Cryo-EM tools into Foldit
合作研究:CIBR:将晶体学和冷冻电镜工具纳入 Foldit
- 批准号:
2051282 - 财政年份:2021
- 资助金额:
$ 31.34万 - 项目类别:
Standard Grant
Collaborative Research: CIBR: The OpenBehavior Project
合作研究:CIBR:开放行为项目
- 批准号:
1948181 - 财政年份:2021
- 资助金额:
$ 31.34万 - 项目类别:
Continuing Grant
Collaborative Research: CIBR: Leaping the Specimen Digitization Gap: Connecting Novel Tools, Machine Learning and Public Participation to Label Digitization Efforts
合作研究:CIBR:跨越标本数字化差距:将新工具、机器学习和公众参与与标签数字化工作联系起来
- 批准号:
2027228 - 财政年份:2021
- 资助金额:
$ 31.34万 - 项目类别:
Standard Grant