作者
Hengxu Mao,Yaoyun Kuang,Feng Du,Xiang Chen,Lin Lu,Wencheng Xia,Tingting Gan,Weimeng Huang,Wenyuan Guo,Hancun Yi,Yirong Yang,Zhuohua Wu,Wei Dai,Hui Sun,Jieyuan Wu,Rui Zhang,Shenqing Zhang,Xiuli Lin,Yuxuan Yong,Xinling Yang,Hongyan Li,Wenjun Wu,Xiaoyun Huang,Zhaoxiang Bian,Hoi Leong Xavier Wong,Xinlu Wang,Michael Poppell,Yi Ren,Cong Liu,Wen‐Quan Zou,Shengdi Chen,Pingyi Xu
摘要
Seed amplification assays (SAA) enable the amplification of pathological misfolded proteins, including α-synuclein (αSyn), in both tissue homogenates and body fluids of Parkinson's disease (PD) patients. SAA involves repeated cycles of shaking or sonication coupled with incubation periods. However, this amplification scheme has limitations in tracking protein propagation due to repeated fragmentation.