Explore the words cloud of the MolMap project. It provides you a very rough idea of what is the project "MolMap" about.
The following table provides information about the project.
Coordinator |
LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN
Organization address contact info |
Coordinator Country | Germany [DE] |
Total cost | 1˙695˙000 € |
EC max contribution | 1˙695˙000 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2015-STG |
Funding Scheme | ERC-STG |
Starting year | 2016 |
Duration (year-month-day) | from 2016-04-01 to 2021-03-31 |
Take a look of project's partnership.
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1 | LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN | DE (MUENCHEN) | coordinator | 1˙695˙000.00 |
Fluorescence microscopy is a powerful tool for exploring biomolecules in cells and tissues, especially with the advent of super-resolution techniques. To better understand key processes such as cell differentiation and disease progression, it is crucial to investigate the abundance, localization and mutual interactions of crucial cellular components such as nucleic acids and proteins. Unraveling their complex interplay in whole signaling networks is necessary to investigate cellular responses to stimuli. However, currently available characterization techniques are either limited by low multiplexing capability (e.g. fluorescence microscopy) or lack localization information (e.g. mass spectrometry). Despite the immense biological and clinical relevance of understanding network-wide changes, the lack of a technological platform to image, identify and quantify a multitude of key protein networks at high spatial resolution in tissues impedes our understanding of the molecular basis of health and disease. I aim to solve this pressing issue and revolutionize fluorescence microscopy using tools from DNA Nanotechnology with transformative potential to positively answer the question: Can we localize and identify each protein or nucleic acid molecule in a complex tissue microenvironment? The approach is based on my recently developed DNA- and Exchange-PAINT techniques. To push the envelope of what’s technically possible I will first build a lattice light-sheet microscope for deep tissue high throughput DNA-PAINT imaging. Second, I will develop novel nanobody- and aptamer-based labeling approaches in combination with molecular barcoding and automated multiplexed image acquisition and processing. With these disruptive and transformative tools, I will investigate whole signaling cascades at once in single cells and whole tissues, thus enabling quantitative imaging transcriptomics and proteomics with highest spatial resolution.
year | authors and title | journal | last update |
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2017 |
Sarit S. Agasti, Yu Wang, Florian Schueder, Aishwarya Sukumar, Ralf Jungmann, Peng Yin DNA-barcoded labeling probes for highly multiplexed Exchange-PAINT imaging published pages: 3080-3091, ISSN: 2041-6520, DOI: 10.1039/c6sc05420j |
Chemical Science 8/4 | 2019-06-19 |
2018 |
Maximilian T. Strauss, Florian Schueder, Daniel Haas, Philipp C. Nickels, Ralf Jungmann Quantifying absolute addressability in DNA origami with molecular resolution published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-018-04031-z |
Nature Communications 9/1 | 2019-06-19 |
2017 |
Florian Schueder, Maximilian T. Strauss, David Hoerl, Joerg Schnitzbauer, Thomas Schlichthaerle, Sebastian Strauss, Peng Yin, Hartmann Harz, Heinrich Leonhardt, Ralf Jungmann Universal Super-Resolution Multiplexing by DNA Exchange published pages: 4052-4055, ISSN: 1433-7851, DOI: 10.1002/anie.201611729 |
Angewandte Chemie International Edition 56/14 | 2019-06-19 |
2018 |
Thomas Schlichthaerle, Alexandra S. Eklund, Florian Schueder, Maximilian T. Strauss, Christian Tiede, Alistair Curd, Jonas Ries, Michelle Peckham, Darren C. Tomlinson, Ralf Jungmann Site-Specific Labeling of Affimers for DNA-PAINT Microscopy published pages: 11060-11063, ISSN: 1433-7851, DOI: 10.1002/anie.201804020 |
Angewandte Chemie International Edition 57/34 | 2019-04-18 |
2018 |
Sebastian Strauss, Philipp C. Nickels, Maximilian T. Strauss, Vilma Jimenez Sabinina, Jan Ellenberg, Jeffrey D. Carter, Shashi Gupta, Nebojsa Janjic, Ralf Jungmann Modified aptamers enable quantitative sub-10-nm cellular DNA-PAINT imaging published pages: 685-688, ISSN: 1548-7091, DOI: 10.1038/s41592-018-0105-0 |
Nature Methods 15/9 | 2019-04-18 |
2017 |
Alexander Auer, Maximilian T. Strauss, Thomas Schlichthaerle, Ralf Jungmann Fast, Background-Free DNA-PAINT Imaging Using FRET-Based Probes published pages: 6428-6434, ISSN: 1530-6984, DOI: 10.1021/acs.nanolett.7b03425 |
Nano Letters 17/10 | 2019-04-18 |
2017 |
Johannes B. Woehrstein, Maximilian T. Strauss, Luvena L. Ong, Bryan Wei, David Y. Zhang, Ralf Jungmann, Peng Yin Sub–100-nm metafluorophores with digitally tunable optical properties self-assembled from DNA published pages: e1602128, ISSN: 2375-2548, DOI: 10.1126/sciadv.1602128 |
Science Advances 3/6 | 2019-04-18 |
2018 |
Jonas Mücksch, Philipp Blumhardt, Maximilian T. Strauss, Eugene P. Petrov, Ralf Jungmann, Petra Schwille Quantifying Reversible Surface Binding via Surface-Integrated Fluorescence Correlation Spectroscopy published pages: 3185-3192, ISSN: 1530-6984, DOI: 10.1021/acs.nanolett.8b00875 |
Nano Letters 18/5 | 2019-04-18 |
2017 |
Florian Schueder, Juanita Lara-Gutiérrez, Brian J. Beliveau, Sinem K. Saka, Hiroshi M. Sasaki, Johannes B. Woehrstein, Maximilian T. Strauss, Heinrich Grabmayr, Peng Yin, Ralf Jungmann Multiplexed 3D super-resolution imaging of whole cells using spinning disk confocal microscopy and DNA-PAINT published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-017-02028-8 |
Nature Communications 8/1 | 2019-04-18 |
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The information about "MOLMAP" are provided by the European Opendata Portal: CORDIS opendata.