ArticlemicroPublication biology2026
3-iodotyrosine fluorescent proteins for improved expansion microscopy.
Article in microPublication biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
10 authors.
Funding
Abstract
Expansion microscopy is a powerful technique for achieving nanoscale resolution, but labelling and detection using fluorescent proteins (FPs) have been hampered by signal degradation during expansion. Current approaches therefore rely heavily on immunostaining, ssDNA-FISH or HALO/SNAP-based detection systems. Here we show that substituting tyrosine with 3-iodotyrosine in the chromophore of superfolder GFP dramatically improves signal retention during expansion microscopy in zebrafish embryos. This enhancement specifically protects FPs during the formaldehyde-dependent anchoring step, and may additionally reflect better tolerance of the prolonged acidic conditions encountered during anchoring. 3-iodotyrosine-modified FPs open a door to reliable protein-based expansion microscopy.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.