Analyzing protein dynamics from fluorescence intensity traces using unsupervised deep learning network

被引:6
|
作者
Yuan, Jinghe [1 ]
Zhao, Rong [2 ]
Xu, Jiachao [1 ]
Cheng, Ming [1 ]
Qin, Zidi [3 ]
Kou, Xiaolong [1 ]
Fang, Xiaohong [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Res Educ Ctr Excellence Mol Sci, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
[2] Natl Inst Metrol, Div Chem Metrol & Analyt Sci, Beijing 100029, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
HIDDEN MARKOV MODEL; SINGLE; RECEPTOR; DIFFUSION; TRACKING; STEPS; STOICHIOMETRY; RATES;
D O I
10.1038/s42003-020-01389-z
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We propose an unsupervised deep learning network to analyze the dynamics of membrane proteins from the fluorescence intensity traces. This system was trained in an unsupervised manner with the raw experimental time traces and synthesized ones, so neither predefined state number nor pre-labelling were required. With the bidirectional Long Short-Term Memory (biLSTM) networks as the hidden layers, both the past and future context can be used fully to improve the prediction results and can even extract information from the noise distribution. The method was validated with the synthetic dataset and the experimental dataset of monomeric fluorophore Cy5, and then applied to extract the membrane protein interaction dynamics from experimental data successfully. Yuan et al. propose an unsupervised deep learning network approach to analyze the dynamics of membrane proteins from the fluorescence intensity traces. The unsupervised nature facilitates training of the system without predefined state number or pre-labelling and can even extract information from noise distribution.
引用
收藏
页数:10
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