ArticlebioRxiv : the preprint server for biology2025
Rewiring protein function through genetically encoded oxidative chemistry.
Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Updated by
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oxidative chemistry underlies many natural signaling pathways but remains largely unexplored as a design strategy for synthetic control of protein function. Here we introduce genetically encoded oxidative modulation as a general mechanism for regulating protein activity in living cells. Using the genetically encodable photosensitizer miniSOG to generate reactive oxygen species (ROS), we show that controlled oxidation alters the behavior of diverse proteins. miniSOG-derived ROS increased the fluorescence of the redox reporter HyPerRed and activated redox-sensitive ion channels TRPV1 and TRPA1, with TRPA1 displaying the strongest response. The magnitude and kinetics were tunable by illumination parameters, expression ratios, and subcellular localization of miniSOG, with membrane anchoring markedly improving efficiency of activating a membrane receptor. These findings establish genetically encoded oxidative chemistry as a versatile and tunable modality for controlling protein function.
Identifiers
What OpenQuestion holds
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.