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帕金森病患者唾液蛋白聚集体的单分子表征:一项初步研究。

Single-molecule characterization of salivary protein aggregates from Parkinson's disease patients: a pilot study.

作者信息

Furlepa Martin, Zhang Yu P, Lobanova Evgeniia, Kahanawita Lakmini, Vivacqua Giorgio, Williams-Gray Caroline H, Klenerman David

机构信息

Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, UK.

Department of Clinical Neurosciences, University of Cambridge, Cambridge CB2 0PY, UK.

出版信息

Brain Commun. 2024 May 21;6(3):fcae178. doi: 10.1093/braincomms/fcae178. eCollection 2024.

Abstract

Saliva is a convenient and accessible biofluid that has potential as a future diagnostic tool for Parkinson's disease. Candidate diagnostic tests for Parkinson's disease to date have predominantly focused on measurements of α-synuclein in CSF, but there is a need for accurate tests utilizing more easily accessible sample types. Prior studies utilizing saliva have used bulk measurements of salivary α-synuclein to provide diagnostic insight. Aggregate structure may influence the contribution of α-synuclein to disease pathology. Single-molecule approaches can characterize the structure of individual aggregates present in the biofluid and may, therefore, provide greater insight than bulk measurements. We have employed an antibody-based single-molecule pulldown assay to quantify salivary α-synuclein and amyloid-β peptide aggregate numbers and subsequently super-resolved captured aggregates using direct Stochastic Optical Reconstruction Microscopy to describe their morphological features. We show that the salivary α-synuclein aggregate/amyloid-β aggregate ratio is increased almost 2-fold in patients with Parkinson's disease ( = 20) compared with controls ( = 20, < 0.05). Morphological information also provides insight, with saliva from patients with Parkinson's disease containing a greater proportion of larger and more fibrillar amyloid-β aggregates than control saliva ( < 0.05). Furthermore, the combination of count and morphology data provides greater diagnostic value than either measure alone, distinguishing between patients with Parkinson's disease ( = 17) and controls ( = 18) with a high degree of accuracy (area under the curve = 0.87, < 0.001) and a larger dynamic range. We, therefore, demonstrate for the first time the application of highly sensitive single-molecule imaging techniques to saliva. In addition, we show that aggregates present within saliva retain relevant structural information, further expanding the potential utility of saliva-based diagnostic methods.

摘要

唾液是一种方便获取的生物流体,有潜力成为未来帕金森病的诊断工具。迄今为止,针对帕金森病的候选诊断测试主要集中在脑脊液中α-突触核蛋白的测量,但需要利用更容易获取的样本类型进行准确测试。此前利用唾液的研究使用了唾液α-突触核蛋白的整体测量来提供诊断见解。聚集结构可能会影响α-突触核蛋白对疾病病理的作用。单分子方法可以表征生物流体中单个聚集体的结构,因此可能比整体测量提供更深入的见解。我们采用了基于抗体的单分子下拉分析来量化唾液α-突触核蛋白和淀粉样β肽聚集体的数量,随后使用直接随机光学重建显微镜对捕获的聚集体进行超分辨率成像,以描述它们的形态特征。我们发现,与对照组(n = 20)相比,帕金森病患者(n = 20)的唾液α-突触核蛋白聚集体/淀粉样β聚集体比率几乎增加了2倍(P < 0.05)。形态学信息也提供了见解,帕金森病患者的唾液中含有比对照唾液更大比例的更大且更纤维化的淀粉样β聚集体(P < 0.05)。此外,计数和形态学数据的结合比单独的任何一种测量都具有更大的诊断价值,能够以高度准确性区分帕金森病患者(n = 17)和对照组(n = 18)(曲线下面积 = 0.87,P < 0.001),并且具有更大的动态范围。因此,我们首次证明了高灵敏度单分子成像技术在唾液中的应用。此外,我们表明唾液中存在的聚集体保留了相关的结构信息,进一步扩大了基于唾液的诊断方法的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12b3/11166177/66e2130551c4/fcae178_ga.jpg

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