Liganded magnetic nanoparticles for magnetic resonance imaging of α-synuclein.

用于α-突触核蛋白磁共振成像的配体磁性纳米粒子

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作者:Pan Hope, Balbirnie Melinda, Hou Ke, Sta Maria Naomi S, Sahay Shruti, Denver Paul, Lepore Stefano, Jones Mychica, Zuo Xiaohong, Zhu Chunni, Mirbaha Hilda, Shahpasand-Kroner Hedieh, Mekkittikul Marisa, Lu Jiahui, Hu Carolyn J, Cheng Xinyi, Abskharon Romany, Sawaya Michael R, Williams Christopher K, Vinters Harry V, Jacobs Russell E, Harris Neil G, Cole Gregory M, Frautschy Sally A, Eisenberg David S
Aggregation of the protein α-synuclein (α-syn) is the histopathological hallmark of neurodegenerative diseases such as Parkinson's disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy (MSA), which are collectively known as synucleinopathies. Currently, patients with synucleinopathies are diagnosed by physical examination and medical history, often at advanced stages of disease. Because synucleinopathies are associated with α-syn aggregates, and α-syn aggregation often precedes onset of symptoms, detecting α-syn aggregates would be a valuable early diagnostic for patients with synucleinopathies. Here, we design a liganded magnetic nanoparticle (LMNP) functionalized with an α-syn-targeting peptide to be used as a magnetic resonance imaging (MRI)-based biomarker for α-syn. Our LMNPs bind to aggregates of α-syn in vitro, cross the blood-brain barrier in mice with mannitol adjuvant, and can be used as an MRI contrast agent to distinguish mice with α-synucleinopathy from age-matched, wild-type control mice in vivo. These results provide evidence for the potential of magnetic nanoparticles that target α-syn for diagnosis of synucleinopathies.

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