I-Corps: Microfluidics for Protein Crystallization and X-ray Diffraction
I-Corps:用于蛋白质结晶和 X 射线衍射的微流体
基本信息
- 批准号:1848428
- 负责人:
- 金额:$ 5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-09-15 至 2020-02-29
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The broader impact/commercial potential of this I-Corps project is to provide pharmaceutical companies and life scientists with a cost effective and fast approach for determining the high-resolution protein structure by X-ray crystallography. Production of high-resolution structures of proteins is one the main steps in structure-based drug design. Although cost reduction and efficiency improvements are the important benefits of structure-based drug design, the lack of generalized methods for high quality, fast and low-cost crystal production is still a major struggle in this process. Microfluidics, is a powerful liquid handling tool that reduces the amount of solution in a screening experiment to nanoliters, have been introduced to the protein crystallization market earlier. However, none of these approaches have penetrated the market because of the high cost to performance ratio. Our innovation is an x-ray transparent microfluidic chip for protein crystallization which is less expensive, easier to operate and more performant in comparison to the current market solutions. By commercializing this device and introducing it to the market, pharmaceutical companies and life scientists will reduce the time and money spent to determine the high-resolution structure of proteins from x-ray diffraction, which is a current bottleneck in structure-based drug discovery.This I-Corps project introduces an inexpensive, x-ray transparent microfluidic chip for protein crystallization. For many medical and biological applications, such as pharmaceutical engineering, the molecular structure of a protein is essential. The most accurate way to determine protein structure is X-ray crystallography, a process that requires the analysis of X-ray diffraction patterns of protein crystals. However, protein crystallization remains challenging because each protein has its own phase diagram, thus, many different conditions should be tried to find the optimal conditions for protein crystallization. Our technology addresses four core challenges in protein crystallization; it (1) screens chemical conditions for protein crystal stability, (2) produces crystals using optimized processing kinetics, (3) obtains structure with room temperature crystals, and (4) avoids crystal handling by diffracting on chip. On-chip X-ray diffraction has been demonstrated for our protein crystallization chips. Prototypes of our first design have been made and have been tested for protein crystallization with one specific solution. Our design is a liquid handling chip with multiple advantages over current microfluidic chips. It is built from inexpensive bio-compatible material via a rapid fabrication procedure and it can be altered as needed based on the customer need.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.
该 I-Corps 项目更广泛的影响/商业潜力是为制药公司和生命科学家提供一种经济有效且快速的方法,用于通过 X 射线晶体学确定高分辨率蛋白质结构。蛋白质高分辨率结构的产生是基于结构的药物设计的主要步骤之一。尽管降低成本和提高效率是基于结构的药物设计的重要好处,但缺乏高质量、快速和低成本晶体生产的通用方法仍然是这一过程的主要难题。微流体是一种功能强大的液体处理工具,可将筛选实验中的溶液量减少至纳升,较早被引入蛋白质结晶市场。然而,由于性价比较高,这些方法都没有进入市场。我们的创新是一种用于蛋白质结晶的 X 射线透明微流控芯片,与当前市场解决方案相比,它更便宜、更易于操作且性能更高。通过将该设备商业化并将其推向市场,制药公司和生命科学家将减少通过 X 射线衍射确定蛋白质高分辨率结构所花费的时间和金钱,这是目前基于结构的药物发现的瓶颈。I-Corps 项目引入了一种用于蛋白质结晶的廉价、X 射线透明微流控芯片。 对于许多医学和生物应用,例如制药工程,蛋白质的分子结构至关重要。确定蛋白质结构最准确的方法是 X 射线晶体学,该过程需要分析蛋白质晶体的 X 射线衍射图案。 然而,蛋白质结晶仍然具有挑战性,因为每种蛋白质都有自己的相图,因此,应该尝试许多不同的条件来找到蛋白质结晶的最佳条件。我们的技术解决了蛋白质结晶的四个核心挑战;它(1)筛选蛋白质晶体稳定性的化学条件,(2)使用优化的加工动力学生产晶体,(3)获得室温晶体的结构,以及(4)通过芯片上的衍射避免晶体处理。我们的蛋白质结晶芯片已证实了片上 X 射线衍射。我们第一个设计的原型已经制作完成,并使用一种特定的解决方案进行了蛋白质结晶测试。我们的设计是一种液体处理芯片,与当前的微流控芯片相比具有多种优势。它由廉价的生物相容性材料通过快速制造程序制成,并且可以根据客户需求进行更改。该奖项反映了 NSF 的法定使命,并通过使用基金会的智力优点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)
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Seth Fraden其他文献
An Arduino-based constant pressure fluid pump
- DOI:
10.1140/epje/s10189-020-00002-9 - 发表时间:
2021-03-08 - 期刊:
- 影响因子:2.200
- 作者:
Theodore Lupinski;Markus Ludwig;Seth Fraden;Nathan Tompkins - 通讯作者:
Nathan Tompkins
Angular correlations and the isotropic-nematic phase transition in suspensions of tobacco mosaic virus.
烟草花叶病毒悬浮液中的角度相关性和各向同性向列相变。
- DOI:
10.1103/physreve.48.2816 - 发表时间:
1993 - 期刊:
- 影响因子:0
- 作者:
Seth Fraden;Georg Maret;D. L. D. Caspar - 通讯作者:
D. L. D. Caspar
A single-molecule microscopy assay for kinetics of DNA origami self-assembly on lipid bilayers
- DOI:
10.1016/j.bpj.2023.11.3369 - 发表时间:
2024-02-08 - 期刊:
- 影响因子:
- 作者:
Nick Berg;Pragya Arora;Rupam Saha;Steven D. Planitzer;Ed Partlow;Tijana Ivanovic;Seth Fraden - 通讯作者:
Seth Fraden
Seth Fraden的其他文献
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{{ truncateString('Seth Fraden', 18)}}的其他基金
PFI-TT: Improved microfluidic devices for protein crystallization and x-ray diffraction
PFI-TT:改进的用于蛋白质结晶和 X 射线衍射的微流体装置
- 批准号:
1919094 - 财政年份:2019
- 资助金额:
$ 5万 - 项目类别:
Standard Grant
The role of boundaries in 2D active nematics
边界在二维活性向列中的作用
- 批准号:
1810077 - 财政年份:2018
- 资助金额:
$ 5万 - 项目类别:
Continuing Grant
2015 Soft Condensed Matter Physics: Self-Assembly and Active Matter GRC/GRS
2015年软凝聚态物理:自组装和活性物质GRC/GRS
- 批准号:
1501169 - 财政年份:2015
- 资助金额:
$ 5万 - 项目类别:
Standard Grant
DMREF: Programmable Chemomechanical Materials
DMREF:可编程化学机械材料
- 批准号:
1534890 - 财政年份:2015
- 资助金额:
$ 5万 - 项目类别:
Standard Grant
MRI: Acquisition of a Multiphoton Microscope for Biomaterials Studies
MRI:购买多光子显微镜用于生物材料研究
- 批准号:
1428238 - 财政年份:2014
- 资助金额:
$ 5万 - 项目类别:
Standard Grant
Collaborative Research: Materials World Network: Protein Phase Behavior - Experiments and Simulations.
合作研究:材料世界网络:蛋白质相行为 - 实验和模拟。
- 批准号:
1209518 - 财政年份:2012
- 资助金额:
$ 5万 - 项目类别:
Continuing Grant
Constraints and Frustration in Nano-Structured and Bio-Molecular Materials
纳米结构和生物分子材料的限制和挫折
- 批准号:
0820492 - 财政年份:2008
- 资助金额:
$ 5万 - 项目类别:
Cooperative Agreement
IDBR: Closed-Loop Protein Crystallization
IDBR:闭环蛋白质结晶
- 批准号:
0754769 - 财政年份:2008
- 资助金额:
$ 5万 - 项目类别:
Continuing Grant
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