丙酮酸激酶缺乏
丙酮酸激酶
巴基斯坦卢比
变构调节
丙酮酸脱氢酶激酶
生物化学
溶血性贫血
红细胞
酶
激酶
激活剂(遗传学)
丙酮酸脱氢酶复合物
化学
糖酵解
生物
分子生物学
内科学
医学
免疫学
基因
作者
Charles Kung,Jeff Hixon,Penelope A. Kosinski,Giovanni Cianchetta,Gavin Histen,Yue Chen,Collin Hill,Stefan Größ,Yaguang Si,Kendall Johnson,Byron DeLaBarre,Zhiyong Luo,Zhiwei Gu,Gui Lan Yao,Huachun Tang,Cheng Fang,YingXia Xu,Xiaobing Lv,Scott A. Biller,Shinsan M. Su
出处
期刊:Blood
[Elsevier BV]
日期:2017-08-01
卷期号:130 (11): 1347-1356
被引量:127
标识
DOI:10.1182/blood-2016-11-753525
摘要
Pyruvate kinase (PK) deficiency is a rare genetic disease that causes chronic hemolytic anemia. There are currently no targeted therapies for PK deficiency. Here, we describe the identification and characterization of AG-348, an allosteric activator of PK that is currently in clinical trials for the treatment of PK deficiency. We demonstrate that AG-348 can increase the activity of wild-type and mutant PK enzymes in biochemical assays and in patient red blood cells treated ex vivo. These data illustrate the potential for AG-348 to restore the glycolytic pathway activity in patients with PK deficiency and ultimately lead to clinical benefit.
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