Department of Electrical and Computer Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Minnesota Center for Prion Research and Outreach, University of Minnesota, St. Paul, Minnesota 55108, United States.
Nano Lett. 2024 Nov 27;24(47):15016-15024. doi: 10.1021/acs.nanolett.4c03768. Epub 2024 Nov 1.
A hallmark of α-synucleinopathies (e.g., Parkinson's disease) is the misfolding and aggregation of α-synuclein in tissues and biological fluids. Protein amplification assays like real-time quaking-induced conversion (RT-QuIC) are sensitive yet currently limited to semi-invasive sample types such as cerebrospinal fluid because more accessible samples, such as blood, contain inhibitors. Here, we show that Nanoparticle-enhanced Quaking-induced Conversion (Nano-QuIC) can double the speed of reactions spiked with misfolded α-synuclein while increasing sensitivity 100-fold in human plasma. Nano-QuIC detected spike concentrations down to 90 pg/mL in lysed whole blood, while reactions without nanoparticles (RT-QuIC) failed to have any detection due to the presence of strong inhibitors. Moreover, Nano-QuIC showed increased seeding activity in plasma samples from Parkinson's patients (n = 4) versus healthy controls (n = 4). This sets the groundwork for the noninvasive diagnostic use of Nano-QuIC, potentially enabling early disease detection and management through blood-based testing.
α-突触核蛋白病(如帕金森病)的一个标志是α-突触核蛋白在组织和生物液中的错误折叠和聚集。实时液流诱导转换(RT-QuIC)等蛋白扩增检测法虽然灵敏,但目前仅限于半侵入性样本类型,如脑脊液,因为更易获得的样本,如血液,含有抑制剂。在这里,我们表明,纳米颗粒增强的液流诱导转换(Nano-QuIC)可以将错误折叠的α-突触核蛋白的反应速度提高一倍,同时在人血浆中的灵敏度提高 100 倍。Nano-QuIC 在裂解全血中检测到低至 90pg/mL 的 spike 浓度,而没有纳米颗粒的反应(RT-QuIC)由于存在强抑制剂而无法进行任何检测。此外,Nano-QuIC 在帕金森病患者(n=4)与健康对照组(n=4)的血浆样本中显示出更高的种子活性。这为 Nano-QuIC 的非侵入性诊断用途奠定了基础,通过血液检测可能实现早期疾病检测和管理。