Evidence map›Paper›PMID 41355246›Full record

ArticleBiophysical journal2026

Quantifying activation delay and the Cole-More shift via current derivatives.

Bernardo I Pinto-Anwandter, Francisco Bezanilla

Erratum issuedAbstract read
In one paragraph

Article in Biophysical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Bernardo I Pinto-AnwandterDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, Illinois. Electronic address: pintobi@uchicago.edu.
Francisco BezanillaDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, Illinois; Centro Interdisciplinario de Neurociencias de Valparaiso, Universidad de Valparaiso, Valparaiso, Chile. Electronic address: fbezanilla@uchicago.edu.

Funding

The Electrophysiological Studies of Voltage Gated ChannelsR01GM030376 · NIGMS · UNIVERSITY OF CHICAGO · PI BEZANILLA, FRANCISCO J · 1985 to 2025
$9.1M
NIGMS NIH HHS R01 GM030376
6 · The paper itself

Abstract

The kinetics of ion channels arise from transitions through multiple closed and open states. An example is the sigmoidal activation kinetics exhibited by voltage-gated potassium channels upon depolarization. This activation sigmoidicity or delay is commonly attributed to the number of closed states that the channel needs to traverse before opening. The Cole-Moore shift refers to the change in this delay upon the magnitude of the hyperpolarization before the activation, and it is empirically obtained by extrapolation of an exponential fit to the time of zero current or by calculating a time shift of the activation kinetics in comparison to a reference trace. However, these methods require selecting analysis windows, determining fitting parameters, or choosing alignment thresholds and do not provide a closed form expression for the Cole-Moore shift or activation delay, complicating the integration of delay measurements into kinetic modeling of ion channels. Here we propose the use of the time derivative of the current (dI/dt) as a straightforward way to obtain the delay before opening and characterize the Cole-Moore shift. In the presence of sigmoidal activation kinetics, the derivative of the current shows a maximum that corresponds to the inflection point (where the second derivative of open probability with respect to time is zero), offering a generalizable descriptor of activation delay. The derivative is useful when obtaining the delay even in the presence of inactivation or multicomponent kinetics as shown in experiments with the Shaker voltage-gated potassium channel. We propose that measuring the maximum of the current derivative provides a simple, quantitative, and broadly applicable tool for analyzing the activation delay and Cole-Moore shift, and we demonstrate its application to voltage-gated channels in systems with different activation and inactivation properties.

Indexed as

Ion Channel GatingModels, BiologicalPotassium Channels, Voltage-GatedAnimalsKineticsTime FactorsPotassium Channels, Voltage-Gated

Identifiers

PMID41355246
PMCPMC12777653

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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.