BayesTICS: Local temporal image correlation spectroscopy and Bayesian simulation technique for sparse estimation of diffusion in fluorescence imaging.

Biological imaging Pub Date : 2023-02-27 eCollection Date: 2023-01-01 DOI:10.1017/S2633903X23000041
Anca Caranfil, Yann Le Cunff, Charles Kervrann
{"title":"BayesTICS: Local temporal image correlation spectroscopy and Bayesian simulation technique for sparse estimation of diffusion in fluorescence imaging.","authors":"Anca Caranfil, Yann Le Cunff, Charles Kervrann","doi":"10.1017/S2633903X23000041","DOIUrl":null,"url":null,"abstract":"<p><p>The dynamics and fusion of vesicles during the last steps of exocytosis are not well established yet in cell biology. An open issue is the characterization of the diffusion process at the plasma membrane. Total internal reflection fluorescence microscopy (TIRFM) has been successfully used to analyze the coordination of proteins involved in this mechanism. It enables to capture dynamics of proteins with high frame rate and reasonable signal-to-noise values. Nevertheless, methodological approaches that can analyze and estimate diffusion in local small areas at the scale of a single diffusing spot within cells, are still lacking. To address this issue, we propose a novel correlation-based method for local diffusion estimation. As a starting point, we consider Fick's second law of diffusion that relates the diffusive flux to the gradient of the concentration. Then, we derive an explicit parametric model which is further fitted to time-correlation signals computed from regions of interest (ROI) containing individual spots. Our modeling and Bayesian estimation framework are well appropriate to represent isolated diffusion events and are robust to noise, ROI sizes, and localization of spots in ROIs. The performance of BayesTICS is shown on both synthetic and real TIRFM images depicting Transferrin Receptor proteins.</p>","PeriodicalId":72371,"journal":{"name":"Biological imaging","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10936362/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1017/S2633903X23000041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The dynamics and fusion of vesicles during the last steps of exocytosis are not well established yet in cell biology. An open issue is the characterization of the diffusion process at the plasma membrane. Total internal reflection fluorescence microscopy (TIRFM) has been successfully used to analyze the coordination of proteins involved in this mechanism. It enables to capture dynamics of proteins with high frame rate and reasonable signal-to-noise values. Nevertheless, methodological approaches that can analyze and estimate diffusion in local small areas at the scale of a single diffusing spot within cells, are still lacking. To address this issue, we propose a novel correlation-based method for local diffusion estimation. As a starting point, we consider Fick's second law of diffusion that relates the diffusive flux to the gradient of the concentration. Then, we derive an explicit parametric model which is further fitted to time-correlation signals computed from regions of interest (ROI) containing individual spots. Our modeling and Bayesian estimation framework are well appropriate to represent isolated diffusion events and are robust to noise, ROI sizes, and localization of spots in ROIs. The performance of BayesTICS is shown on both synthetic and real TIRFM images depicting Transferrin Receptor proteins.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
BayesTICS:荧光成像中扩散稀疏估计的局部时间图像相关光谱和贝叶斯模拟技术
胞吐过程中囊泡的动力学和融合在细胞生物学中尚未得到很好的证实。一个悬而未决的问题是质膜上扩散过程的表征。全内反射荧光显微镜(TIRFM)已经成功地用于分析参与这一机制的蛋白质的协调。它能够以高帧率和合理的信噪比值捕获蛋白质的动态。然而,在细胞内单个扩散点的尺度上,可以分析和估计局部小区域扩散的方法学方法仍然缺乏。为了解决这个问题,我们提出了一种新的基于相关性的局部扩散估计方法。作为起点,我们考虑菲克第二扩散定律,它将扩散通量与浓度梯度联系起来。然后,我们推导了一个显式参数模型,该模型进一步拟合了从包含单个点的感兴趣区域(ROI)计算的时间相关信号。我们的建模和贝叶斯估计框架非常适合于表示孤立的扩散事件,并且对噪声、ROI大小和ROI中的点定位具有鲁棒性。BayesTICS的性能显示在合成和真实的TIRFM图像上,描绘了转铁蛋白受体蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Reconstructing interpretable features in computational super-resolution microscopy via regularized latent search. Algebraic Constraints and Algorithms for Common Lines in Cryo-EM TomoNet: A streamlined cryogenic electron tomography software pipeline with automatic particle picking on flexible lattices. GoldDigger and Checkers, computational developments in cryo-scanning transmission electron tomography to improve the quality of reconstructed volumes Alignment of density maps in Wasserstein distance.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1