Advanced image-free analysis of the nano-organization of chromatin and other biomolecules by Single Molecule Localization Microscopy (SMLM)

被引:8
|
作者
Weidner, Jonas [1 ]
Neitzel, Charlotte [1 ]
Gote, Martin [1 ,3 ]
Deck, Jeanette [1 ]
Kuentzelmann, Kim [1 ]
Pilarczyk, Goetz [1 ]
Falk, Martin [1 ,2 ]
Hausmann, Michael [1 ]
机构
[1] Heidelberg Univ, Kirchhoff Inst Phys, Neuenheimer Feld 227, D-69120 Heidelberg, Germany
[2] Czech Acad Sci, Inst Biophys, Kralovopolska 135, Brno 61200, Czech Republic
[3] Katholieke Univ Leuven, Anim & Human Hlth Engn, Kasteelpk Arenberg 30, B-3001 Leuven, Belgium
关键词
Single molecule localization microscopy; (SMLM); Ripley distance frequency histograms; Persistent homology; Persistent image; Principal component analysis; Application of mathematical analysis tools to; chromatin organization and DNA repair; processes; DNA-DAMAGE; GENOME REGULATION; CELLS; REPAIR; RESOLUTION; COMPLEXITY; DYNAMICS; SPDM;
D O I
10.1016/j.csbj.2023.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cell as a system of many components, governed by the laws of physics and chemistry drives molecular functions having an impact on the spatial organization of these systems and vice versa. Since the re-lationship between structure and function is an almost universal rule not only in biology, appropriate methods are required to parameterize the relationship between the structure and function of biomolecules and their networks, the mechanisms of the processes in which they are involved, and the mechanisms of regulation of these processes. Single molecule localization microscopy (SMLM), which we focus on here, offers a significant advantage for the quantitative parametrization of molecular organization: it provides matrices of coordinates of fluorescently labeled biomolecules that can be directly subjected to advanced mathematical analytical procedures without the need for laborious and sometimes misleading image processing. Here, we propose mathematical tools for comprehensive quantitative computer data analysis of SMLM point patterns that include Ripley distance frequency analysis, persistent homology analysis, per-sistent 'imaging', principal component analysis and co-localization analysis. The application of these methods is explained using artificial datasets simulating different, potentially possible and interpretatively important situations. Illustrative analyses of real complex biological SMLM data are presented to emphasize the applicability of the proposed algorithms. This manuscript demonstrated the extraction of features and parameters quantifying the influence of chromatin (re)organization on genome function, offering a novel approach to study chromatin architecture at the nanoscale. However, the ability to adapt the proposed algorithms to analyze essentially any molecular organizations, e.g., membrane receptors or protein traf-ficking in the cytosol, offers broad flexibility of use. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. This is an open access article under the CC BY-NC-ND license (http://creative-commons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:2018 / 2034
页数:17
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