Antonios Pantazis lab

@antoniospantazis.bsky.social

Sr. assoc. prof. in #ionchannel physiology & #channelopathy at Linköping University. Ever excited about the proteins that control excitability. https://liu.se/en/research/palace

Can one map the genome-wide binding (1) and its protein partners (2) simultaneously from the same sample? Yes, one can. with CUT&ID ✂️🪪 Spearheaded — singlehandedly — by @annanordin.bsky.social No need of transgenesis, cloning and overexpression. Check it out, it's fast and its works.

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bioRxivpreprint@biorxivpreprint.bsky.social · 9mo ago

CUT&ID for simultaneous profiling of protein-DNA and protein-protein interactions https://www.biorxiv.org/content/10.64898/2025.12.11.693662v1

Very excited to share our most recent work on using de novo design to custom engineer a small peptide that can restore proper sodium channel function in disease … to be able to “write” proteins to do whatever we want them to do, is just remarkable …

Cell - a Cell Press journal@cp-cell.bsky.social · last yr.

Now online! De novo design of a peptide modulator to reverse sodium channel dysfunction linked to cardiac arrhythmias and epilepsy

Out now at Nat Comm: "A rich conformational palette 🎨 underlies human CaV2.1-channel availability" 1. VSD-I activation triggers transmitter release 2. VSD-I conversion causes VDI & contributes to plasticity 3. CaV2.1 channels have several conformations at Vrest #neuroskyence #CACNA1A rdcu.be/ei0Tm

A rich conformational palette underlies human CaV2.1-channel availability

Nature Communications - CaV2.1 channels are critical for neuronal communication. Here, authors showed they undergo electrically-evoked molecular movements which (1) eventually trigger...

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