Systematic,spatial imaging of large multimolecular assemblies and the emerging principles of supramolecular order in biological systems |
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| Authors: | Walter Schubert |
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| Affiliation: | 1. Molecular pattern recognition research group, O‐v‐G‐university Magdeburg, Germany;2. International faculty, Max‐Planck (CAS‐MPG) partner institute for computational biology, Shanghai, China;3. Human toponome project, TNL, Munich, Germany |
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| Abstract: | Understanding biological systems at the level of their relational (emergent) molecular properties in functional protein networks relies on imaging methods, able to spatially resolve a tissue or a cell as a giant, non‐random, topologically defined collection of interacting supermolecules executing myriads of subcellular mechanisms. Here, the development and findings of parameter‐unlimited functional super‐resolution microscopy are described—a technology based on the fluorescence imaging cycler (IC) principle capable of co‐mapping thousands of distinct biomolecular assemblies at high spatial resolution and differentiation (<40 nm distances). It is shown that the subcellular and transcellular features of such supermolecules can be described at the compositional and constitutional levels; that the spatial connection, relational stoichiometry, and topology of supermolecules generate hitherto unrecognized functional self‐segmentation of biological tissues; that hierarchical features, common to thousands of simultaneously imaged supermolecules, can be identified; and how the resulting supramolecular order relates to spatial coding of cellular functionalities in biological systems. A large body of observations with IC molecular systems microscopy collected over 20 years have disclosed principles governed by a law of supramolecular segregation of cellular functionalities. This pervades phenomena, such as exceptional orderliness, functional selectivity, combinatorial and spatial periodicity, and hierarchical organization of large molecular systems, across all species investigated so far. This insight is based on the high degree of specificity, selectivity, and sensitivity of molecular recognition processes for fluorescence imaging beyond the spectral resolution limit, using probe libraries controlled by ICs. © 2013 The Authors. Journal of Molecular Recognition published by John Wiley & Sons, Ltd. |
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| Keywords: | supermolecules functional super‐resolution fluorescence imaging toponome imaging cycler MELC TIS toponome imaging system |
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