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Assessing the impact of minimizing arginine conversion in fully defined SILAC culture medium in human embryonic stem cells

机译:评估在人类胚胎干细胞中完全定义的SILAC培养基中最小化精氨酸转化的影响

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摘要

We present a fully defined culture system (adapted Essential8TM [E8TM] medium in combination with vitronectin) for human embryonic stem cells that can be used for SILAC purposes. Although a complete incorporation of the labels was observed after 4 days in culture, over 90% of precursors showed at least 10% conversion. To reduce this arginine conversion, E8TM medium was modified by adding (1) l‐proline, (2) l‐ornithine, (3) Nω‐hydroxy‐nor‐l‐arginine acetate, or by (4) lowering the arginine concentration. Reduction of arginine conversion was best obtained by adding 5 mM l‐ornithine, followed by 3.5 mM l‐proline and by lowering the arginine concentration in the medium to 99.5 μM. No major changes in pluripotency and cell amount could be observed for the adapted E8TM media with ornithine and proline. However, our subsequent ion mobility assisted data‐independent acquisition (high‐definition MS) proteome analysis cautions for ongoing changes in the proteome when aiming at longer term suppression of arginine conversion.
机译:我们为人类胚胎干细胞提供了一种完全定义的培养系统(适应性Essential8 TM [E8 TM ]培养基和玻连蛋白),可用于SILAC。尽管在培养4天后观察到标记完全掺入,但超过90%的前体显示出至少10%的转化率。为了减少这种精氨酸转化,通过添加(1)l-脯氨酸,(2)l-鸟氨酸,(3)N ω -hydroxy-nor来修饰E8 TM 培养基-l-精氨酸乙酸盐,或通过(4)降低精氨酸浓度。降低精氨酸转化率的最佳方法是加入5 mM l-鸟氨酸,然后添加3.5 mM l-脯氨酸,并将培养基中的精氨酸浓度降低至99.5μM。带有鸟氨酸和脯氨酸的改良E8 TM 培养基在多能性和细胞数量方面没有观察到重大变化。但是,我们的后续离子迁移辅助数据无关的采集(高清MS)蛋白质组分析为长期抑制精氨酸转化提供了蛋白质组中不断变化的警告。

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