首页> 外文会议>ASMS Conference on Mass Spectrometry and Allied Topics >Mapping proteolytic peptide production rates in plasma using stable isotope labeled proteins from the SILAC-labeled HepG2 secretome
【24h】

Mapping proteolytic peptide production rates in plasma using stable isotope labeled proteins from the SILAC-labeled HepG2 secretome

机译:使用稳定的同位素从硅酸标记的HepG2综合标记的蛋白质中标记蛋白质的蛋白质溶解肽产生速率

获取原文

摘要

Demonstrated the potential for using HepG2 cells for generation of stable isotope labeled plasma proteins for MS-based quantification. >60 intact stable isotope labeled plasma proteins generated, including complex apolipoproteins from non-depleted plasma. Strategies to improve coverage of lower abundant proteins are being explored. SILAC HepG2 peptide cocktail allowed >3500 peptides from >60 plasma proteins to be monitored over time with 745 suitable PABST H/L peptide pairs identified. Broad range of isotopically labeled peptides formed (596), with high PABST suitability scores for PRM based experiments.
机译:证明了使用HepG2细胞产生稳定同位素标记的等离子体蛋白的潜力,用于MS基量化。 > 60完整的稳定同位素标记标记的等离子体蛋白,包括来自非耗尽血浆的复合载蛋白。正在探讨改善较低丰富蛋白质覆盖的策略。允许H745鉴定的745个合适的PABST H / L肽对,允许从> 60血浆蛋白允许> 3500肽。宽范围的同位素标记的肽形成(596),具有高PABST适合性评分,用于PRM基础实验。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号