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3D Bayesian cluster analysis of super-resolution data reveals LAT recruitment to the T cell synapse

机译:超分辨率数据的3D贝叶斯聚类分析显示LAT募集到T细胞突触

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摘要

Single-molecule localisation microscopy (SMLM) allows the localisation of fluorophores with a precision of 10–30 nm, revealing the cell’s nanoscale architecture at the molecular level. Recently, SMLM has been extended to 3D, providing a unique insight into cellular machinery. Although cluster analysis techniques have been developed for 2D SMLM data sets, few have been applied to 3D. This lack of quantification tools can be explained by the relative novelty of imaging techniques such as interferometric photo-activated localisation microscopy (iPALM). Also, existing methods that could be extended to 3D SMLM are usually subject to user defined analysis parameters, which remains a major drawback. Here, we present a new open source cluster analysis method for 3D SMLM data, free of user definable parameters, relying on a model-based Bayesian approach which takes full account of the individual localisation precisions in all three dimensions. The accuracy and reliability of the method is validated using simulated data sets. This tool is then deployed on novel experimental data as a proof of concept, illustrating the recruitment of LAT to the T-cell immunological synapse in data acquired by iPALM providing ~10 nm isotropic resolution.
机译:单分子定位显微镜(SMLM)可使荧光团定位的精度为10–30nm,从而在分子水平上揭示细胞的纳米级结构。最近,SMLM已扩展到3D,从而提供了对蜂窝机械的独特见解。尽管已经为2D SMLM数据集开发了聚类分析技术,但很少将其应用于3D。定量工具的缺乏可以通过成像技术(如干涉光激活定位显微镜(iPALM))的相对新颖性来解释。同样,可以扩展到3D SMLM的现有方法通常要遵循用户定义的分析参数,这仍然是一个主要缺点。在这里,我们依靠基于模型的贝叶斯方法提出了一种新的用于3D SMLM数据的开源聚类分析方法,该方法没有用户定义的参数,该方法充分考虑了所有三个维度上的各个定位精度。使用模拟数据集验证了该方法的准确性和可靠性。然后将该工具部署到新的实验数据上作为概念验证,说明了iPALM提供的〜10nm nm各向同性分辨率的数据中,LAT向T细胞免疫突触的募集。

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