Introducing deuterium for next generation chemical biology probes and direct imaging
This project aims to revolutionize microscopy by using deuterated compounds for super-resolution imaging and drug tracking in live cells, enhancing protein localization and neural signaling without genetic modifications.
Projectdetails
Introduction
The ideal microscopy experiment would take place in native cells without genetic engineering, with 3-dimensional resolution on the single molecule scale (<10 nm) by observing the endogenous molecule itself.
Proposed Methodology
I propose the introduction and use of deuterium (“deuterON”) as a general method for a multimodal approach, to:
- Synthesize a first-in-class deuterated cyanine (Cy) fluorophore for super-resolution imaging.
- Design and test deuterated, next-level photoswitches to restore vision.
- Use these probes and deuterated drugs for direct and bioorthogonal, spectroscopic imaging.
Applications in Microscopy
In particular, deuterated Cys will allow stochastic reconstruction microscopy (STORM) by using near infra-red light to break new ground in protein localization in live tissue. This approach opens the gates for thick sample imaging (~100 m axial) with retained super-resolution (~20 nm).
Development of Photoswitches
Additionally, deuterated azobenzene photoswitches will be designed to finally reach the indispensable, and to-date unobtained light sensitivity to remote control neural signaling in vivo.
Label-Free Imaging
Lastly, the use of "label-free" labeling and imaging will be explored with deuterated drugs to observe drug uptake and metabolism by utilizing the unique properties of the carbon-deuterium bond in Raman spectroscopy. Coupled to a confocal microscope, deuterated drugs will be tracked in native and live cells, without any genetic engineering strategies, and on the molecule of interest itself, reducing perturbations and artifacts to a minimum.
Conclusion
This ground-breaking approach holds promise to be generalizable to Chemical Biology disciplines, and serves as an unconventional, yet attractive and powerful method to design and synthesize next-generation small molecule probes. Developing a pipeline for these aims will be a game changer, with ramifications for the life sciences, cell biology, drug development, and with prospective translational impact.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.499.469 |
Totale projectbegroting | € 1.499.469 |
Tijdlijn
Startdatum | 1-9-2022 |
Einddatum | 31-8-2027 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- FORSCHUNGSVERBUND BERLIN EVpenvoerder
Land(en)
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Time-based single molecule nanolocalization for live cell imaging
The project aims to develop a novel live-cell nanoscopy technique that enables high-speed, high-resolution imaging of biological processes at the nanoscale without compromising depth or volume.
Deuterium labeling of GLUCOse improves magnetic resonance imaging Sensitivity to CANcer metabolism
GLUCO-SCAN aims to develop and clinically evaluate a novel whole-body deuterium metabolic imaging (DMI) method for cancer assessment, overcoming PET's limitations and enabling widespread screening.
Super-resolution Field-Resolved Stimulated Raman Microscopy
This project aims to develop a super-resolution, label-free Raman microscope using femtosecond laser technology to non-invasively visualize subcellular structures with unprecedented sensitivity and resolution.
Lensless label-free nanoscopy
This project aims to develop deep UV lensless holotomographic nanoscopy for high-resolution, large-field imaging of live cells to enhance understanding of extracellular vesicles as disease biomarkers.
Linker molecules convert commercial fluorophores into tailored functional probes during biolabeling
The project aims to enhance the performance of fluorescent probes by developing versatile linker compounds that improve labeling properties for biomedical applications, reducing costs and increasing reliability.
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