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First steps towards effective methods in exploiting high-throughput technologies for the determination of human protein structures of high biomedical value.

机译:迈向开发高通量技术以确定具有高生物医学价值的人蛋白质结构的有效方法的第一步。

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摘要

The EC 'Structural Proteomics In Europe' contract is aimed specifically at the atomic resolution structure determination of human protein targets closely linked to health, with a focus on cancer (kinesins, kinases, proteins from the ubiquitin pathway), neurological development and neurodegenerative diseases and immune recognition. Despite the challenging nature of the analysis of such targets, approximately 170 structures have been determined to date. Here, the impact of high-throughput technologies, such as parallel expression of multiple constructs, the use of standardized refolding protocols and optimized crystallization screens or the use of mass spectrometry to assist sample preparation, on the structural biology of mammalian protein targets is illustrated through selected examples.
机译:EC的“欧洲结构蛋白质组学”合同专门针对确定与健康紧密相关的人类蛋白质靶标的原子分辨结构,重点关注癌症(驱动蛋白,激酶,遍在蛋白途径中的蛋白质),神经系统发育和神经退行性疾病以及免疫识别。尽管对此类目标进行分析具有挑战性,但迄今为止已确定了约170个结构。在此,通过以下方式说明了高通量技术对哺乳动物蛋白质靶标结构生物学的影响,例如多种构建体的平行表达,使用标准化的折叠协议和优化的结晶筛选或使用质谱法协助样品制备。选定的例子。

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