- Engineered an orthogonal electrical synapse from white perch connexins Cx34.7 and Cx35 to enable selective intercellular electrical coupling in mammalian circuits
- Combined protein mutagenesis, in vitro docking assay and computational modelling to identify a structural motif enabling specific hemichannel docking and preventing cross-interaction with native connexins
- Validated LinCx in vivo in C. elegans and mice, showing strengthened communication and behaviour changes, enabling long term circuit editing in mammals
Nature. 2026 May 13. doi: 10.1038/s41586-026-10501-y. Online ahead of print.
ABSTRACT
Electrical signalling across distinct populations of brain cells underpins cognitive and emotional function. However, approaches that selectively regulate electrical signalling between two cellular components of a mammalian neural circuit remain sparse. Here we engineered an electrical synapse composed of two connexin proteins1 found in Morone americana (white perch fish)-connexin 34.7 and connexin 35-to accomplish mammalian circuit modulation. By exploiting protein mutagenesis, devising a new in vitro system for assaying connexin hemichannel docking, and performing computational modelling of hemichannel interactions, we uncovered a structural motif that contributes to electrical synapse formation. Targeting this motif, we designed connexin 34.7 and connexin 35 hemichannels that dock with each other to form an electrical synapse but not with other major connexins expressed in the mammalian central nervous system. We validated this electrical synapse in vivo using worms (Caenorhabditis elegans) and mice (Mus musculus). We demonstrate that it can strengthen communication across neural circuits composed of pairs of distinct cell types and modify behaviour accordingly. Thus, we establish ‘long-term integration of circuits using connexins’ (LinCx) for precision circuit editing in mammals.
PMID:42129559 | DOI:10.1038/s41586-026-10501-y
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