Microfluidic technologies for high-throughput monocIonal antibody selection from single cells
用于从单细胞中选择高通量单克隆抗体的微流控技术
基本信息
- 批准号:351319-2008
- 负责人:
- 金额:$ 5.83万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Collaborative Health Research Projects
- 财政年份:2009
- 资助国家:加拿大
- 起止时间:2009-01-01 至 2010-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
This project will bring together two research groups with complementary expertise led by Dr. John Schrader, a medically-trained, internationally recognized immunologist, and Dr. Carl Hansen a physicist and engineer who is a leader in innovation in the new science of microfluidics. Together these interdisciplinary teams will develop a novel and innovative device that will address a pivotal problem in basic and applied medical research - the rapid and inexpensive generation of high-value monoclonal antibodies. Monoclonal antibodies are counterparts of the antibodies in our blood that protect us from infections by binding to viruses or toxins and are responsible for immunity to diseases we have encountered before. Antibodies have the unique property thai they come in millions of different shapes. A "monoclonal antibody " is a pure preparation of one antibody with its one particular shape and different monoclonal antibodies can be selected to fight a virus or target a cancer. Monoclonal antibodies are the fastest growing class of new therapeutic agents and are providing breakthrough treatments e.g for cancers of the breast, colon, lymphatic tissues and others (Herceptin, Erbitux, Rituximab, Avastin) and arthritis and Crohn's disease (Remicade, Humira). The ability to find a monoclonal antibody that selectively binds to virtually any substance is also of enormous medical and commercial importance in the diagnosis of disease and in biomedical research. Despite this enormous potential, the discovery and production of high-quality antibodies by conventional means is a major bottleneck. Current techniques are expensive, require months or years of development, and are not compatible with the production of antibodies that can be easily used in humans. This project will merge state-of-the-art techniques in microengineering, immunology, and biophotonics to enable a postage stamp-size device to make sensitive measurements on the antibodies made by thousands of single cells and copy the genetic recipes for antibodies with useful characteristics, so that they can be made in unlimited quantities as human or rabbit monoclonal antibodies for use as therapies or as reagents. The results of the research should lead to exciting commercial opportunities.
该项目将汇集两个具有互补专业知识的研究小组,由医学训练有素的国际公认免疫学家John Schrader博士和物理学家兼工程师Carl Hansen博士领导,他是微流体新科学创新的领导者。这些跨学科团队将共同开发一种新颖和创新的设备,将解决基础和应用医学研究中的关键问题-快速和廉价地产生高价值的单克隆抗体。单克隆抗体是我们血液中抗体的对应物,通过与病毒或毒素结合来保护我们免受感染,并负责对我们以前遇到的疾病产生免疫力。抗体具有独特的性质,它们有数百万种不同的形状。“单克隆抗体”是一种具有特定形状的抗体的纯制剂,可以选择不同的单克隆抗体来对抗病毒或靶向癌症。单克隆抗体是发展最快的一类新型治疗药物,为乳腺癌、结肠癌、淋巴组织和其他癌症(赫赛汀、爱必妥、利妥昔单抗、阿瓦斯汀)以及关节炎和克罗恩病(Remicade、Humira)提供了突破性的治疗方法。在疾病诊断和生物医学研究中,找到一种选择性结合几乎任何物质的单克隆抗体的能力也具有巨大的医学和商业重要性。尽管有巨大的潜力,但通过传统手段发现和生产高质量抗体是一个主要瓶颈。目前的技术价格昂贵,需要数月或数年的开发,并且与易于用于人类的抗体的生产不兼容。该项目将融合微工程、免疫学和生物光子学等最先进的技术,使邮票大小的设备能够对数千个单细胞产生的抗体进行敏感测量,并复制具有有用特征的抗体的遗传配方,从而可以无限量地制造人类或兔子单克隆抗体,用于治疗或试剂。这项研究的结果将带来令人兴奋的商业机会。
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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Schrader, John其他文献
Ankle Strength and Force Sense After a Progressive, 6-Week Strength-Training Program in People With Functional Ankle Instability
- DOI:
10.4085/1062-6050-47.3.06 - 发表时间:
2012-05-01 - 期刊:
- 影响因子:3.3
- 作者:
Smith, Brent I.;Docherty, Carrie L.;Schrader, John - 通讯作者:
Schrader, John
Prevalence of chronic ankle instability in high school and division I athletes.
- DOI:
10.1177/1938640013509670 - 发表时间:
2014-02-01 - 期刊:
- 影响因子:0
- 作者:
Tanen, Leah;Docherty, Carrie L;Schrader, John - 通讯作者:
Schrader, John
Severity of Functional and Mechanical Ankle Instability in an Active Population
- DOI:
10.3113/fai.2009.1071 - 发表时间:
2009-11-01 - 期刊:
- 影响因子:2.7
- 作者:
Hirai, Derek;Docherty, Carrie L.;Schrader, John - 通讯作者:
Schrader, John
Functional performance testing in participants with functional ankle instability and in a healthy control group
- DOI:
10.4085/1062-6050-43.4.342 - 发表时间:
2008-07-01 - 期刊:
- 影响因子:3.3
- 作者:
Buchanan, Amanda S.;Docherty, Carrie L.;Schrader, John - 通讯作者:
Schrader, John
Schrader, John的其他文献
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{{ truncateString('Schrader, John', 18)}}的其他基金
The Role of M-Ras in Social Recognition
M-Ras 在社会认可中的作用
- 批准号:
436257-2013 - 财政年份:2017
- 资助金额:
$ 5.83万 - 项目类别:
Discovery Grants Program - Individual
The Role of M-Ras in Social Recognition
M-Ras 在社会认可中的作用
- 批准号:
436257-2013 - 财政年份:2016
- 资助金额:
$ 5.83万 - 项目类别:
Discovery Grants Program - Individual
The Role of M-Ras in Social Recognition
M-Ras 在社会认可中的作用
- 批准号:
436257-2013 - 财政年份:2015
- 资助金额:
$ 5.83万 - 项目类别:
Discovery Grants Program - Individual
The Role of M-Ras in Social Recognition
M-Ras 在社会认可中的作用
- 批准号:
436257-2013 - 财政年份:2014
- 资助金额:
$ 5.83万 - 项目类别:
Discovery Grants Program - Individual
Generation of a rabbit monoclonal antibody that discriminates between acetyl amantadine and amantadine
区分乙酰金刚烷胺和金刚烷胺的兔单克隆抗体的产生
- 批准号:
452021-2013 - 财政年份:2013
- 资助金额:
$ 5.83万 - 项目类别:
Engage Grants Program
The Role of M-Ras in Social Recognition
M-Ras 在社会认可中的作用
- 批准号:
436257-2013 - 财政年份:2013
- 资助金额:
$ 5.83万 - 项目类别:
Discovery Grants Program - Individual
Microfluidic technologies for high-throughput monocIonal antibody selection from single cells
用于从单细胞中选择高通量单克隆抗体的微流控技术
- 批准号:
351319-2008 - 财政年份:2010
- 资助金额:
$ 5.83万 - 项目类别:
Collaborative Health Research Projects
Microfluidic technologies for high-throughput monocIonal antibody selection from single cells
用于从单细胞中选择高通量单克隆抗体的微流控技术
- 批准号:
351319-2008 - 财政年份:2008
- 资助金额:
$ 5.83万 - 项目类别:
Collaborative Health Research Projects
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