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Proteomic Profiling of Secreted Proteins from CHO Cells Using Surface-Enhanced Laser Desorption Ionization Time-of-Flight Mass Spectrometry

机译:使用表面增强激光解吸电离飞行时间质谱从CHO细胞中进行蛋白质组蛋白分析

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摘要

Chinese hamster ovary (CHO) cells are the most commonly used host cell line for the production\udof recombinant biopharmaceuticals. These biopharmaceuticals are typically secreted from CHO\udcells and purified from harvested cell culture media. The purpose of this study was to investigate\udchanges in the secreted proteome of CHO cells over the various stages of the growth cycle\udusing Surface Enhanced Laser desorption ionization time-of-flight mass spectrometry (SELDITOF\udMS). Conditioned media samples were collected each day over a 6 day growth period\udfrom CHO-K1 cells grown in low serum (0.5% FBS) conditions in monolayer culture. Samples\udwere profiled on a number of ProteinChip arrays with different chromatographic surfaces. From\udthis study, 24 proteins were found to be differentially regulated at different phases of the growth\udcycle in CHO-K1 cells, when profiled on two chromatographic surfaces, Q10 (anionic) and\udIMAC30 (metal affinity) ProteinChip arrays.
机译:中国仓鼠卵巢(CHO)细胞是用于生产重组生物药物的最常用宿主细胞系。这些生物药物通常从CHO \ udcell分泌,并从收获的细胞培养基中纯化。这项研究的目的是研究\在生长周期的各个阶段CHO细胞分泌的蛋白质组中的变化\使用表面增强激光解吸电离飞行时间质谱(SELDITOF \ udMS)。在6天的生长期内,每天收集条件培养基样品,这些样品来自单层培养的低血清(0.5%FBS)条件下生长的CHO-K1细胞。在具有不同色谱表面的许多ProteinChip阵列上对样品进行了分析。从这项研究中,发现在两个色谱表面Q10(阴离子)和udIMAC30(金属亲和力)ProteinChip阵列上进行分析时,在CHO-K1细胞的不同生长阶段中,有24种蛋白质受到不同的调控。

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