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Destabilized near-infrared fluorescent nanobodies enable background-free targeting of GFP-based biosensors for imaging and manipulation.
- Source :
- Nature Communications; 9/6/2024, Vol. 15 Issue 1, p1-16, 16p
- Publication Year :
- 2024
-
Abstract
- Near-infrared (NIR) probes are highly sought after as fluorescent tags for multicolor cellular and in vivo imaging. Here we develop small NIR fluorescent nanobodies, termed NIR-Fb<subscript>LAG16</subscript> and NIR-Fb<subscript>LAG30</subscript>, enabling background-free visualization of various GFP-derived probes and biosensors. We also design a red-shifted variant, NIR-Fb<subscript>(718)</subscript>, to simultaneously target several antigens within the NIR spectral range. Leveraging the antigen-stabilizing property of the developed NIR-Fbs, we then create two modular systems for precise control of gene expression in GFP-labeled cells. Applying the NIR-Fbs in vivo, we target cells expressing GFP and the calcium biosensor GCaMP6 in the somatosensory cortex of transgenic mice. Simultaneously tracking calcium activity and the reference signal from NIR-Fb<subscript>LAG</subscript>s bound to GCaMP6 enables ratiometric deep-brain in vivo imaging. Altogether, NIR-Fb<subscript>LAG</subscript>s present a promising approach for imaging and manipulating various processes in live cells and behaving animals expressing GFP-based probes. Near-infrared (NIR) probes are in high demand as fluorescent tags for multicolour cellular and in vivo imaging. Here authors develop series of NIR nanobodies that bind to GFP-based biosensors, and demonstrate ratiometric deep-brain in vivo imaging of active GCaMP6f-expressing neurons. [ABSTRACT FROM AUTHOR]
- Subjects :
- CELL imaging
IMMUNOGLOBULINS
TRANSGENIC mice
BIOSENSORS
GENE expression
Subjects
Details
- Language :
- English
- ISSN :
- 20411723
- Volume :
- 15
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Nature Communications
- Publication Type :
- Academic Journal
- Accession number :
- 179504782
- Full Text :
- https://doi.org/10.1038/s41467-024-51857-x