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Colin Nichols Lab

@colinnicholslab.bsky.social
337 followers 710 following 45 posts

Posting from Colin Nichols' electrophysiology lab at WashU. Focused on ion channels biophysics & role in physiology and pathology.

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Colin Nichols Lab @colinnicholslab.bsky.social · 14/09/2026
New lab members, new lab pic! 🧪
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Colin Nichols Lab @colinnicholslab.bsky.social · 27/08/2026
Check out our new publication "Cognitive Decline, Neurologic Involvement, and Neonatal Crisis in ABCC9-Related Intellectual Disability and Myopathy Syndrome" 🧪 www.neurology.org/doi/10.1212/...
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Reposted by Colin Nichols Lab
Journal of General Physiology @jgp.org · 22/06/2026
Will the real KATP please stand up? Kir6.2/SUR2A takes the stand in the tiring case of #SkeletalMuscle fatigue. @rainbowlabuol.bsky.social and @richardbj.bsky.social discuss new work from Scala and Chen et al. @colinnicholslab.bsky.social (rupress.org/jgp/article/...): rupress.org/jgp/article/...
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Reposted by Colin Nichols Lab
Journal of General Physiology @jgp.org · 27/05/2026
Subunit composition of the KATP channels that modulate contractility of skeletal muscle during fatigue. New study from Rosa Scala, Yuezhou Chen, Colin G. Nichols @colinnicholslab.bsky.social and colleagues @washumedicine.bsky.social: rupress.org/jgp/article/... #SkeletalMuscle #IonChannels
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Reposted by Colin Nichols Lab
Rockefeller University Press @rupress.org · 20/05/2026
In @jgp.org: Using specific gene subunit knockout mice, Scala and Chen et al. @colinnicholslab.bsky.social show that KATP channels formed exclusively of SUR2/Kir6.2 cause delayed fatigue and development of unstimulated force in isolated EDL skeletal muscles rupress.org/jgp/article/...
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Colin Nichols Lab @colinnicholslab.bsky.social · 03/03/2026
Check out our latest review "From Selective Permeation to Physiology in Potassium Channels" 🧪 journals.physiology.org/doi/full/10....
journals.physiology.org
From Selective Permeation to Physiology in Potassium Channels | Function | American Physiological Society
Abstract Highly K+-selective potassium channels are essential for electrical signaling. The high selectivity of most K+ channels, with relative K+: Na+ permeabilities being as high as 100–1000:1 arises from the conserved so-called K+ channel selectivity filter (SF). Structural and computational studies have shown how the SF forms multiple sites that coordinate K+, by mimicking the water dipoles that coordinate K+ ions in solution, and thermodynamically favoring the binding of K+ over Na+. Selective conduction of K+ ions then results from a “knock-on” mechanism, whereby entering ions destabilize the next ion in the file. This review highlights key biophysical and biochemical research that provides insights to the atomic details of these processes. It then discusses how mutations that alter K+ selectivity and permeation in different K+ channels underlie multiple simple and complex diseases, illustrating how selectivity and permeation are central to physiology and to pathophysiology and important for physiologists to be aware of.
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Colin Nichols Lab @colinnicholslab.bsky.social · 03/03/2026
Check out our new publication "Cantu syndrome–associated SUR2[H60Y] mutation confers selective gain of function on Kir6.1 ATP-sensitive potassium channels" 🧪 www.jbc.org/article/S002... A 🧵 1/n
jbc.org
Cantu syndrome–associated SUR2[H60Y] mutation confers selective gain of function on Kir6.1 ATP-sensitive potassium channels
Gain-of-function (GOF) mutations in either Kir6.1 (encoded by KCNJ8) or SUR2 (encoded by ABCC9) are causally associated with Cantu syndrome (CS), characterized by coarse facial appearance, hypertricho...
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Reposted by Colin Nichols Lab
Journal of General Physiology @jgp.org · 14/10/2025
Muscle fatigue arising intrinsically from SUR2- but not Kir6.1-dependent gain-of-function in Cantu syndrome mice. A new study from Rosa Scala, Colin Nichols et al. @colinnicholslab.bsky.social rupress.org/jgp/article/... #IonChannels #MolecularPhysiology #Pathophysiology #SkeletalMuscle
rupress.org
Muscle fatigue arising intrinsically from SUR2- but not Kir6.1-dependent gain-of-function in Cantu syndrome mice
We assessed skeletal muscle properties in GOF knock-in mouse models of Cantu Syndrome. In isolated myofibers there was enhanced Mg-nucleotide activation in
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Reposted by Colin Nichols Lab
Journal of General Physiology @jgp.org · 10/10/2025
PIP2-driven cytoplasmic domain motions are coupled to Kir2 channel gating, say Eva-Maria Zangerl-Plessl, Anna Stary-Weinzinger, Colin G. Nichols, and Sun-Joo Lee rupress.org/jgp/article/... @colinnicholslab.bsky.social #IonChannels #Phospholipids
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Colin Nichols Lab @colinnicholslab.bsky.social · 07/10/2025
Check out our new publication "Treatment of overactive KATP channels with glibenclamide in a zebrafish model and a clinical trial in humans with Cantú syndrome" 🧪 @nature.com www.nature.com/articles/s41...
nature.com
Treatment of overactive KATP channels with glibenclamide in a zebrafish model and a clinical trial in humans with Cantú syndrome - Scientific Reports
Scientific Reports - Treatment of overactive KATP channels with glibenclamide in a zebrafish model and a clinical trial in humans with Cantú syndrome
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Colin Nichols Lab @colinnicholslab.bsky.social · 07/10/2025
Check out our new publication "Molecular basis of TRPV3 channel blockade by intracellular polyamines" 🧪 www.nature.com/articles/s42...
nature.com
Molecular basis of TRPV3 channel blockade by intracellular polyamines - Communications Biology
Identification of TRPV3 channel residues interacting with intracellular spermine and high resolution structure of a non-conducting TRPV3 in the presence of NASPM suggest a unifying molecular model to explain spermine block of TRPV1-4 channels.
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Reposted by Colin Nichols Lab
Rockefeller University Press @rupress.org · 07/10/2025
In @jgp.org, Scala et al @colinnicholslab.bsky.social assess #SkeletalMuscle properties in gain-of-function knock-in mouse models of Cantu Syndrome. Isolated SUR2 GOF, but not Kir6.1 GOF muscles show enhanced fatiguing that was reversed by the KATP inhibitor glibenclamide
rupress.org
Muscle fatigue arising intrinsically from SUR2- but not Kir6.1-dependent gain-of-function in Cantu syndrome mice
We assessed skeletal muscle properties in GOF knock-in mouse models of Cantu Syndrome. In isolated myofibers there was enhanced Mg-nucleotide activation in
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Colin Nichols Lab @colinnicholslab.bsky.social · 07/10/2025
Check out our new publication "Muscle fatigue arising intrinsically from SUR2- but not Kir6.1-dependent gain-of-function in Cantu syndrome mice" 🧪 @rosca26.bsky.social A 🧵 1/n
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Reposted by Colin Nichols Lab
Rockefeller University Press @rupress.org · 03/10/2025
New in @jgp.org: Zangerl-Plessl, Lee, et al. utilized MD simulations to reveal that PIP2 potentiated clockwise twisting motions in individual Kir2 #IonChannel cytoplasmic subunits, as well as concerted dynamics among the four subunits. rupress.org/jgp/article/... @colinnicholslab.bsky.social
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Colin Nichols Lab @colinnicholslab.bsky.social · 07/10/2025
Check out our new publication "PIP2-driven cytoplasmic domain motions are coupled to Kir2 channel gating" 🧪 A 🧵 1/n
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Colin Nichols Lab @colinnicholslab.bsky.social · 07/10/2025
We love it Stephen, thank you! 🧪
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Colin Nichols Lab @colinnicholslab.bsky.social · 22/05/2025
Check out our new publication "Paradoxical Maturity-Onset Diabetes of the Young Arising From Loss-of-Function Mutations in ATP-Sensitive Potassium Channels" 🧪 diabetesjournals.org/diabetes/art... @rosca26.bsky.social A 🧵 1/n
diabetesjournals.org
Paradoxical Maturity-Onset Diabetes of the Young Arising From Loss-of-Function Mutations in ATP-Sensitive Potassium Channels
Pancreatic β-cell ATP-sensitive K+ (KATP) channel closure underlies electrical excitability and insulin release, but loss or inhibition of KATP channels ca
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Colin Nichols Lab @colinnicholslab.bsky.social · 17/05/2025
Next Monday! 🧪
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Colin Nichols Lab @colinnicholslab.bsky.social · 05/05/2025
Join us today for a new exciting CIMED seminar! 🧪 @osamaharraz.bsky.social
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Colin Nichols Lab @colinnicholslab.bsky.social · 07/04/2025
Join us today for a new exciting CIMED seminar! 🧪
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Colin Nichols Lab @colinnicholslab.bsky.social · 17/03/2025
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Colin Nichols Lab @colinnicholslab.bsky.social · 15/03/2025
Check out our new publication "Dynein light chains 1 and 2 are auxiliary proteins of pH-sensitive Kir4.1 channels" www.sciencedirect.com/science/arti... A 🧵 1/n
sciencedirect.com
Dynein light chains 1 and 2 are auxiliary proteins of pH-sensitive Kir4.1 channels
Inward rectifier Kir4.1 potassium channels are abundantly expressed in cells that are important for electrolyte homeostasis. Dysregulation of Kir4.1 u…
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Colin Nichols Lab @colinnicholslab.bsky.social · 03/03/2025
Join us today for a new exciting CIMED seminar! 🧪
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Colin Nichols Lab @colinnicholslab.bsky.social · 13/02/2025
Join us today for a new exciting CIMED seminar!
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Colin Nichols Lab @colinnicholslab.bsky.social · 28/01/2025
📢 Nichols Lab is hiring! 📢 Join us at WashU & contribute to cutting-edge ion channel research. DM or email nicholslab.wustl.edu
nicholslab.wustl.edu
Discover our work - Colin Nichols Lab
Welcome to the Vitaly Klyachko Lab! We examine synaptic dysfunction in the brain to better understand Alzheimer’s Disease and Fragile Z Syndrome.
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Colin Nichols Lab @colinnicholslab.bsky.social · 23/01/2025
Check out our new publication "Control of neurovascular coupling by ATP-sensitive potassium channels" A 🧵 1 journals.sagepub.com/doi/10.1177/...
journals.sagepub.com
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