<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Michel JC</submitter><funding>NICHD NIH HHS</funding><funding>NEI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Neuronal circuits are composed of synapses that are either chemical, where signals are transmitted via neurotransmitter release and reception, or electrical, where signals pass directly through interneuronal gap junction channels. While the molecular complexity that controls chemical synapse structure and function is well appreciated, the proteins of electrical synapses beyond the gap-junction-forming Connexins are not well defined. Yet, electrical synapses are expected to be molecularly complex beyond the gap junctions. Connexins are integral membrane proteins requiring vesicular transport and membrane insertion/retrieval to achieve function, homeostasis, and plasticity. Additionally, electron microscopy of neuronal gap junctions reveals neighboring electron dense regions termed the elect</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.11.22.624763</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11601576</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Electrical synapse molecular diversity revealed by proximity-based proteomic discovery.</pubmed_title><pmcid>PMC11601576</pmcid><funding_grant_id>F32 HD102182</funding_grant_id><funding_grant_id>P30 CA069533</funding_grant_id><funding_grant_id>R01 NS105758</funding_grant_id><funding_grant_id>P30 EY010572</funding_grant_id><funding_grant_id>T32 GM007413</funding_grant_id><funding_grant_id>R21 NS117967</funding_grant_id><pubmed_authors>Michel JC</pubmed_authors><pubmed_authors>Branon TC</pubmed_authors><pubmed_authors>Miller AC</pubmed_authors><pubmed_authors>Lukowicz-Bedford RM</pubmed_authors><pubmed_authors>Martin EA</pubmed_authors><pubmed_authors>Crow WE</pubmed_authors><pubmed_authors>Kissinger JS</pubmed_authors><pubmed_authors>Horrocks M</pubmed_authors><pubmed_authors>Ting AY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrical synapse molecular diversity revealed by proximity-based proteomic discovery.</name><description>Neuronal circuits are composed of synapses that are either chemical, where signals are transmitted via neurotransmitter release and reception, or electrical, where signals pass directly through interneuronal gap junction channels. While the molecular complexity that controls chemical synapse structure and function is well appreciated, the proteins of electrical synapses beyond the gap-junction-forming Connexins are not well defined. Yet, electrical synapses are expected to be molecularly complex beyond the gap junctions. Connexins are integral membrane proteins requiring vesicular transport and membrane insertion/retrieval to achieve function, homeostasis, and plasticity. Additionally, electron microscopy of neuronal gap junctions reveals neighboring electron dense regions termed the elect</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2025-04-04T02:17:13.078Z</modification><creation>2025-04-04T02:17:13.078Z</creation></dates><accession>S-EPMC11601576</accession><cross_references><pubmed>39605535</pubmed><doi>10.1101/2024.11.22.624763</doi></cross_references></HashMap>