血小板生成素
免疫原性
血小板
重组DNA
生物活性
化学
融合蛋白
肽
刺激
药理学
EC50型
血小板活化
血小板生成素受体
体外
比活度
生物化学
融合
促红细胞生成素
细胞融合
脂质双层融合
免疫学
分子生物学
ED50公司
内在活性
毛茛
巨核细胞
作者
Xinyu Zhao,Yutuo Zheng,Guosheng Gao,Xiaozhen Xu,Airong Hu,Jingjing Ying
摘要
Thrombopoietin (TPO) is essential for treating thrombocytopenia, but its clinical use is limited by immunogenicity and short half-life. TMP, a TPO mimetic peptide, addresses these issues but requires fusion with carriers to improve pharmacokinetics. This study developed ELP-TMP fusion proteins (ELP120-2TMP and 2TMP-ELP120) to extend half-life and enhance activity via elastin-like polypeptide (ELP). Results showed EC50 values of 5.81 n m for ELP120-2TMP and 10.88 n m for 2TMP-ELP120, compared to 2.65 n m for recombinant human TPO (rhTPO). At a dose of 600 nmol/kg, ELP120-2TMP resulted in peak platelet counts in mice on day 20, exhibiting a half-life of 22.9 h. Conversely, 2TMP-ELP120 achieved peak platelet counts on day 12, with a half-life of 25.4 h. The half-lives of both fusion proteins were significantly longer than that reported 2TMP alone (1 h). Area under the curve indicated superior platelet stimulation over rhTPO (P < 0.01).
科研通智能强力驱动
Strongly Powered by AbleSci AI