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用于兴奋剂控制目的的检测氨甲酰化红细胞生成素的分析方法。

The analytical approach for detection of carbamylated erythropoietin for doping control purposes.

机构信息

Polish Anti-Doping Laboratory, Warsaw, Poland.

出版信息

Drug Test Anal. 2020 Nov;12(11-12):1599-1604. doi: 10.1002/dta.2956. Epub 2020 Nov 24.

Abstract

Erythropoietin (EPO) has protective effects in several tissues and could be used for therapeutic purposes, but the doses of EPO that can be beneficial in case of hypoxic-ischemic conditions due to overinduced erythropoiesis could be detrimental in treated patients. Carbamylation of erythropoietin maintains the tissue-protective effects of EPO but without erythropoietic effects. Carbamylated EPO (CEPO) is listed in WADA Prohibited List in class S2 as "Innate repair receptor agonists." The CEPO was synthesized using the method described previously. Digestion with endoproteinase Lys-C was used to distinguish rhEPO from CEPO. The digested samples containing recombinant EPO, urinary EPO (uEPO), or CEPO were analyzed by the SAR-PAGE method (sarcosyl polyacrylamide gel electrophoresis-PAGE). Endoproteinase Lys-C breaks the peptide chains of lysine. Lysine residues, converted to homocitrulline by carbamylation, cannot be cleaved by endoproteinase Lys-C. Therefore, the CEPO protein chain remained unchanged in contrast to rhEPO and uEPO, which allows for easily differentiation of them.

摘要

促红细胞生成素(EPO)在多种组织中具有保护作用,可用于治疗目的,但在缺氧缺血情况下,由于过度诱导红细胞生成而有益的 EPO 剂量可能对治疗患者有害。EPO 的氨甲酰化维持 EPO 的组织保护作用,但没有促红细胞生成作用。氨甲酰化促红细胞生成素(CEPO)被列入世界反兴奋剂机构(WADA)禁用清单 S2 类,作为“先天修复受体激动剂”。CEPO 是使用先前描述的方法合成的。使用内切蛋白酶 Lys-C 消化将 rhEPO 与 CEPO 区分开来。通过 SAR-PAGE 方法(肌氨酸多聚丙烯酰胺凝胶电泳-PAGE)分析含有重组 EPO、尿促红细胞生成素(uEPO)或 CEPO 的消化样品。内切蛋白酶 Lys-C 切断赖氨酸的肽链。赖氨酸残基经氨甲酰化转化为同型瓜氨酸,不能被内切蛋白酶 Lys-C 切割。因此,CEPO 蛋白链与 rhEPO 和 uEPO 相比保持不变,这使得它们易于区分。

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