4.7 Article

Highly Efficient Activatable MRI Probe to Sense Myeloperoxidase Activity

期刊

JOURNAL OF MEDICINAL CHEMISTRY
卷 64, 期 9, 页码 5874-5885

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.1c00038

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资金

  1. NIH [R01 NS103998, K25 HL150305]
  2. National Multiple Sclerosis Society
  3. National Health and Medical Research Council (NHMRC) of Australia
  4. Australian Research Council [170101453]
  5. Australian Academy of Technology and Engineering
  6. NHMRC Senior Principal Research Fellowship
  7. American Society of Neuroradiology (ASNR)

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heMAMP is a highly efficient MPO-activatable MRI probe with improved stability and increased affinity to the active site of MPO. It shows significantly higher contrast-to-noise ratios in animal models of inflammation and unstable atherosclerotic plaques compared to conventional probes, making it a promising candidate for translation to clinical settings.
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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