Liquid handling automated workstation for cell based assays
用于细胞检测的液体处理自动化工作站
基本信息
- 批准号:439328175
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:德国
- 项目类别:Major Research Instrumentation
- 财政年份:2020
- 资助国家:德国
- 起止时间:2019-12-31 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
We are a team of five research groups working on a wide range of topics at the interface between Biology and Medicine, specifically on cell and molecular biology of bacterial pathogens, antimicrobials and antifungals, host-pathogen interactions and cancer biology. While working on largely diverse topics, we share a common goal of applying innovative high-throughput approaches to tackle our research questions. In order to do so, we hereby apply for financial support for establishing a cutting-edge liquid handling automated workstation. With this instrumentation specially designed to develop novel high-throughput cell based assays, we propose to:• Perform a large-scale assessment the bactericidal effect of drug combinations against gram-negative bacterial pathogens, therefore providing new insights for fighting the alarming rise of antibiotic resistance. For a handful of potent synergistic combinations, we propose to re-assess their intracellular efficacy against persistent gram-negative pathogens, which are increasingly acknowledged to cause relapsing infections. The underlying mechanisms of bacterial cell death will be investigated using bacterial mutant libraries and conventional molecular biology techniques.• Explore large compound libraries to systematically investigate i) particular stress-response mechanisms in gastrointestinal bacterial pathogens – efflux pumps, small RNA regulators, small proteins – and how they relate to drug resistance and interaction with the human host; ii) how the host metabolism rewires in response to infection by intracellular pathogens which cause sexually transmitted diseases; iii) potential inhibitors of cancer specific protein-protein interactions.• Establish a large and well-characterised Candida spp. isolate collection, therefore elucidating the current antifungal resistance and epidemiological situation of one of the most prevalent life-threatening fungal pathogens in Germany.The automated workstation – to which we currently have no access – is instrumental to accomplish the described projects, and it would therefore tremendously support our research.
我们是一个由五个研究小组组成的团队,致力于生物学和医学交叉领域的广泛主题,特别是细菌病原体的细胞和分子生物学、抗菌剂和抗真菌剂、宿主-病原体相互作用和癌症生物学。虽然研究的主题多种多样,但我们有一个共同的目标:应用创新的高通量方法来解决我们的研究问题。为此,我们特此申请资金支持,以建立尖端的液体处理自动化工作站。 利用专门设计用于开发新型高通量细胞检测的仪器,我们建议: • 对药物组合对革兰氏阴性细菌病原体的杀菌效果进行大规模评估,从而为对抗令人震惊的抗生素耐药性上升提供新的见解。对于一些有效的协同组合,我们建议重新评估它们对持续性革兰氏阴性病原体的细胞内功效,人们越来越认识到这些病原体会导致复发性感染。将使用细菌突变体库和常规分子生物学技术来研究细菌细胞死亡的潜在机制。•探索大型化合物库以系统地研究i)胃肠道细菌病原体中的特定应激反应机制——外排泵、小RNA调节剂、小蛋白质——以及它们与耐药性和与人类宿主相互作用的关系; ii) 宿主新陈代谢如何重新连接以应对引起性传播疾病的细胞内病原体的感染; iii) 癌症特异性蛋白质-蛋白质相互作用的潜在抑制剂。• 建立一个大型且特征良好的念珠菌属。分离收集,从而阐明德国最常见的威胁生命的真菌病原体之一的当前抗真菌耐药性和流行病学状况。自动化工作站(我们目前无法访问)对于完成所描述的项目至关重要,因此它将极大地支持我们的研究。
项目成果
期刊论文数量(0)
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其他文献
吉治仁志 他: "トランスジェニックマウスによるTIMP-1の線維化促進機序"最新医学. 55. 1781-1787 (2000)
Hitoshi Yoshiji 等:“转基因小鼠中 TIMP-1 的促纤维化机制”现代医学 55. 1781-1787 (2000)。
- DOI:
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LiDAR Implementations for Autonomous Vehicle Applications
- DOI:
- 发表时间:
2021 - 期刊:
- 影响因子:0
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吉治仁志 他: "イラスト医学&サイエンスシリーズ血管の分子医学"羊土社(渋谷正史編). 125 (2000)
Hitoshi Yoshiji 等人:“血管医学与科学系列分子医学图解”Yodosha(涉谷正志编辑)125(2000)。
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Effect of manidipine hydrochloride,a calcium antagonist,on isoproterenol-induced left ventricular hypertrophy: "Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,K.,Teragaki,M.,Iwao,H.and Yoshikawa,J." Jpn Circ J. 62(1). 47-52 (1998)
钙拮抗剂盐酸马尼地平对异丙肾上腺素引起的左心室肥厚的影响:“Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,
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