CCI Phase I: NSF Center for Genomically Encoded Materials (C-GEM)
CCI Phase I: NSF Center for Genomically Encoded Materials (C-GEM)
批准号:
1740549
负责人:
Alanna Schepartz
金额:
$180.0万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2020-03-31
中文摘要
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英文摘要
Developing synthetic routes to polymers consisting of a defined sequence of monomers is a current challenge in chemistry. Proteins are natural polymers, and are specific sequences of amino acids put together easily and efficiently by the living cell. The NSF Center for Genomically Encoded Materials (C-GEM) takes a bio-inspired approach making a sequence of synthetic polymers by re-engineering the cell's systems. In this case, the cell becomes a new translational machine that synthesizes new chemical polymers of specific sequence and length. NSF C-GEM establishes a new, transformative field of chemistry and fosters innovation at the chemistry-biology-materials frontier. The applications of the new materials with novel properties range from information storage to anti-counterfeiting and drug delivery, from environmental remediation to drug discovery. NSF C-GEM engages scientists and non-scientists in a variety of research and educational activities, including improved communication to the public. These education and participation programs integrate research with training to establish a diverse chemical workforce. NSF C-GEM presents a new online platform and data management system, GEM-Net, to promote data sharing within and outside the research team. NSF C-GEM is also developing an online video game that allows citizen scientists to participate in the research process and track results. The NSF Center for Genomically Encoded Materials, NSF C-GEM, is focused on the challenge of preparing polymers whose monomers and dispersity are defined with protein-like control. Sequence-defined polymers possess extraordinary potential for information storage, anti-counterfeiting, drug delivery, environmental remediation, and even drug discovery, but strategies to prepare them are barely in their infancy. NSF C-GEM's approach synthesizes sequence-defined chemical polymers by repurposing the E. coli translational apparatus. The translation machinery, which normally promotes bond formation between alpha-amino acids, now promotes bond-forming reactions between monomers that are the building blocks for aramids, polyolefins, polyurethanes, and other polymers. The approach demands orthogonal enzymes that acylate orthogonal tRNAs with each monomer, efficiently and in vivo; orthogonal ribosomes that accept these tRNAs as substrates and elongate the products; genomically-recoded organisms with multiple open codons to enable mRNA-templated synthesis of sequence-defined polymers; and high-resolution structural data to deepen understanding and inform design. The project develops the multi-disciplinary tools and technologies that demonstrate the proof of concept of the approach and establish practical methodologies to this aim. NSF C-GEM fosters innovation at the chemistry-biology-materials frontier, and engages scientists and non-scientists in research and educational activities. A diverse set of education and participation programs integrates research with training, establishes a diverse chemical workforce, and improves communication with the public.
期刊论文(12)
专著(0)
科研奖励(0)
会议论文
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DOI:
10.1021/acscentsci.9b00460
发表时间:
2019-07-24
期刊:
ACS CENTRAL SCIENCE
影响因子:
18.2
作者:
[Ad, Omer, Hoffman, Kyle S., Schepartz, Alanna]
通讯作者:
Schepartz, Alanna
Foldamers wave to the ribosome
折叠分子向核糖体挥动
DOI:
10.1038/s41557-018-0036-5
发表时间:
2018
期刊:
Nature Chemistry
影响因子:
21.8
作者:
[Schepartz, Alanna]
通讯作者:
Schepartz, Alanna
DOI:
10.1016/j.cbpa.2018.07.020
发表时间:
2018-10
期刊:
Current opinion in chemical biology
影响因子:
7.8
作者:
[Arranz-Gibert P, Vanderschuren K, Isaacs FJ]
通讯作者:
Isaacs FJ
DOI:
10.1038/nbt.4150
发表时间:
2018-08
期刊:
Nature biotechnology
影响因子:
46.9
作者:
[Barber KW, Muir P, Szeligowski RV, Rogulina S, Gerstein M, Sampson JR, Isaacs FJ, Rinehart J]
通讯作者:
Rinehart J
DOI:
10.1038/s41467-021-27836-x
发表时间:
2022-01-10
期刊:
Nature communications
影响因子:
16.6
作者:
[Radford F, Elliott SD, Schepartz A, Isaacs FJ]
通讯作者:
Isaacs FJ
共 7 条
Role of protein unfolding in endosomal escape
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批准号:2203903
-
项目类别:Standard Grant
-
资助金额:$56.7万
-
财政年份:2022
-
负责人:Alanna Schepartz
-
依托单位:
NSF Center for Genetically Encoded Materials
-
批准号:2002182
-
项目类别:Cooperative Agreement
-
资助金额:$2000.0万
-
财政年份:2020
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负责人:Alanna Schepartz
-
依托单位:
CCI Phase I: NSF Center for Genomically Encoded Materials (C-GEM)
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批准号:2021739
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项目类别:Standard Grant
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资助金额:$82.65万
-
财政年份:2019
-
负责人:Alanna Schepartz
-
依托单位:
Sophistication of beta-Peptide Bundle Form and Function
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批准号:0848098
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项目类别:Continuing Grant
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资助金额:$51.4万
-
财政年份:2009
-
负责人:Alanna Schepartz
-
依托单位:
Presidential Young Investigator Award: Bioorganic Chemistry
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批准号:9157486
-
项目类别:Continuing Grant
-
资助金额:$34.5万
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财政年份:1991
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负责人:Alanna Schepartz
-
依托单位:
Determination of the Active Site of Peptidyl-prolyl Isomerase Enzymes Using Peptide-Based Affinity Cleaving Reagents
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批准号:9003527
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项目类别:Standard Grant
-
资助金额:$3.5万
-
财政年份:1990
-
负责人:Alanna Schepartz
-
依托单位:
国内基金
海外基金
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批准号:24ZR1429700
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项目类别:省市级项目
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资助金额:--
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负责人:YUICHIRO NAKAI
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批准号:11961141014
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资助金额:12.0万元
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资助金额:17.4万元
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批准年份:2015
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负责人:陈童
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依托单位:
纳米(I-Phase+α-Mg)准共晶的临界半固态形成条件及生长机制
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资助金额:25.0万元
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批准年份:2012
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负责人:张英波
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依托单位:
连续Phase-Type分布数据拟合方法及其应用研究
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批准号:11101428
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2011
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负责人:黄卓
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依托单位:
D-Phase准晶体的电子行为各向异性的研究
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批准号:19374069
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项目类别:面上项目
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资助金额:6.4万元
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批准年份:1993
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负责人:张殿琳
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依托单位: