髓过氧化物酶
化学
对接(动物)
多塔
细胞毒性
炎症
生物化学
螯合作用
免疫学
体外
医学
生物
护理部
有机化学
作者
Cuihua Wang,David Cheng,Negin Jalali Motlagh,Enrico G. Kuellenberg,Gregory R. Wojtkiewicz,Stephen Schmidt,Roland Stocker,John W. Chen
标识
DOI:10.1021/acs.jmedchem.1c00038
摘要
Myeloperoxidase (MPO) is a key component of innate immunity but can damage tissues when secreted abnormally. We developed a new generation of a highly efficient MPO-activatable MRI probe (heMAMP) to report MPO activity. heMAMP has improved Gd stability compared to bis-5-HT-Gd-DTPA (MPO-Gd) and demonstrates no significant cytotoxicity. Importantly, heMAMP is more efficiently activated by MPO compared to MPO-Gd, 5HT-DOTA(Gd), and 5HT-DOTAGA-Gd. Molecular docking simulations revealed that heMAMP has increased rigidity via hydrogen bonding intramolecularly and improved binding affinity to the active site of MPO. In animals with subcutaneous inflammation, activated heMAMP showed a 2–3-fold increased contrast-to-noise ratio (CNR) compared to activated MPO-Gd and 4–10 times higher CNR compared to conventional DOTA-Gd. This increased efficacy was further confirmed in a model of unstable atherosclerotic plaque where heMAMP demonstrated a comparable signal increase and responsiveness to MPO inhibition at a 3-fold lower dosage compared to MPO-Gd, further underscoring heMAMP as a potential translational candidate.
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