Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Ionic Strength: Overview01:12

Ionic Strength: Overview

3.2K
The ionic strength of a solution is a quantitative way of expressing the total electrolyte concentration of a solution. This concept was first introduced in 1921 by two American physical chemists, Gilbert N. Lewis and Merle Randall, while describing the activity coefficient of strong electrolytes. During the calculation of ionic strength (I or μ), all the cations and anions are considered. However, the concentration (c) of an ion with a greater charge number (z) has a greater contribution...
3.2K
Potentiometry: Membrane Electrodes01:15

Potentiometry: Membrane Electrodes

1.9K
Membrane electrodes, also known as p-ion electrodes, use membranes that selectively interact with free analyte ions, generating a potential difference across the membrane. The resulting membrane potential, known as the asymmetry potential, is not zero even when analyte concentrations on both sides of the membrane are equal. The membrane's response is typically not selective to a single analyte but proportional to the concentration of all ions in the sample solution capable of interacting at...
1.9K
Concentration Cells02:41

Concentration Cells

26.0K
A concentration cell is a type of a  voltaic cell constructed by connecting two almost identical half-cells, both based on the same half-reaction and using the same electrode, differing only in the concentration of one redox species. A concentration cell's potential, therefore, is determined only by the concentration difference of the particular redox species.
Consider the following voltaic cell:
26.0K
Controlled-Potential Coulometry: Electrolytic Methods01:17

Controlled-Potential Coulometry: Electrolytic Methods

767
Controlled-potential coulometry, also known as potentiostatic coulometry, employs a three-electrode system in which the working electrode's potential is precisely regulated using a potentiostat. Platinum working electrodes are utilized for positive potentials, while mercury pool electrodes are favored for extremely negative potentials. The platinum counter electrode is separated from the analyte using a membrane or salt bridge to avoid interference in the analysis.
The chosen potential...
767

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Relationship between body segment movements and center of pressure shifts during trunk lean movements while sitting in healthy adults.

Frontiers in rehabilitation sciences·2026
Same author

Comparative analysis of peptide and protein self-assembly in food systems: Driving forces, influencing factors, structural outcomes, and future prospects.

Food chemistry·2026
Same author

Condition-dependent amorphous protein agglomerates control cytoplasmic rheology.

Molecular cell·2026
Same author

Autonomous Synthesis and Scrambling of Phospholipids, Linked to Recycling of Cofactors in Synthetic Cells.

ACS synthetic biology·2026
Same author

Structural and functional implications of phase separation of membrane protein LacY in Escherichia coli.

Nature communications·2026
Same author

Surface-modified protein crowders influence mutant huntingtin exon 1 aggregation via crowding effects, crowder association, and crowder solution stability.

Protein science : a publication of the Protein Society·2025
Same journal

Inositol Thiophosphates as Inhibitors of Mammalian, Plant, and Fungal Phytases.

ACS chemical biology·2026
Same journal

Synthesis and Characterization of the Spectroscopic and Imaging Utilities of Two Indole-Based Cyan Fluorescent Nucleoside Analogues.

ACS chemical biology·2026
Same journal

Indole Ring Expansion and Rearrangement-Enabled Quinoline Scaffold Formation in the Biosynthesis of the Antitumor Monoterpene Indole Alkaloid Camptothecin.

ACS chemical biology·2026
Same journal

Intracellular Delivery of Peptides and Proteins with an Engineered Membrane Translocation Domain.

ACS chemical biology·2026
Same journal

Development of Next-Generation Fluoroacetamidine-Containing Activity-Based Probes for the Selective Labeling of the Protein Arginine Deiminases (PADs).

ACS chemical biology·2026
Same journal

Spectroelectrochemical Insight into Reaction Mechanisms of Cell-Penetrating Peptides on Charged Membrane Surfaces.

ACS chemical biology·2026
See all related articles

Related Experiment Video

Updated: Feb 23, 2026

Measurement of Extracellular Ion Fluxes Using the Ion-selective Self-referencing Microelectrode Technique
09:18

Measurement of Extracellular Ion Fluxes Using the Ion-selective Self-referencing Microelectrode Technique

Published on: May 3, 2015

14.5K

Ionic Strength Sensing in Living Cells.

Boqun Liu1, Bert Poolman1, Arnold J Boersma1

  • 1Department of Biochemistry, Groningen Biomolecular Sciences and Biotechnology Institute & Zernike Institute for Advanced Materials, University of Groningen , Nijenborgh 4, 9747 AG Groningen, The Netherlands.

ACS Chemical Biology
|August 31, 2017
PubMed
Summary
This summary is machine-generated.

Scientists developed novel protein sensors to measure ionic strength within living cells. This breakthrough allows real-time observation of ionic changes at the single-cell level, advancing in vivo biochemistry understanding.

More Related Videos

Multi-analyte Biochip MAB Based on All-solid-state Ion-selective Electrodes ASSISE for Physiological Research
08:03

Multi-analyte Biochip MAB Based on All-solid-state Ion-selective Electrodes ASSISE for Physiological Research

Published on: April 18, 2013

17.9K
Double-barreled and Concentric Microelectrodes for Measurement of Extracellular Ion Signals in Brain Tissue
11:08

Double-barreled and Concentric Microelectrodes for Measurement of Extracellular Ion Signals in Brain Tissue

Published on: September 5, 2015

14.5K

Related Experiment Videos

Last Updated: Feb 23, 2026

Measurement of Extracellular Ion Fluxes Using the Ion-selective Self-referencing Microelectrode Technique
09:18

Measurement of Extracellular Ion Fluxes Using the Ion-selective Self-referencing Microelectrode Technique

Published on: May 3, 2015

14.5K
Multi-analyte Biochip MAB Based on All-solid-state Ion-selective Electrodes ASSISE for Physiological Research
08:03

Multi-analyte Biochip MAB Based on All-solid-state Ion-selective Electrodes ASSISE for Physiological Research

Published on: April 18, 2013

17.9K
Double-barreled and Concentric Microelectrodes for Measurement of Extracellular Ion Signals in Brain Tissue
11:08

Double-barreled and Concentric Microelectrodes for Measurement of Extracellular Ion Signals in Brain Tissue

Published on: September 5, 2015

14.5K

Area of Science:

  • Biochemistry
  • Cell Biology
  • Biophysics

Background:

  • Understanding intracellular ionic strength is crucial for comprehending the behavior of charged biomacromolecules in their native cellular environment.
  • Existing methods lack the precision and real-time capabilities to assess ionic strength within living cells.

Purpose of the Study:

  • To develop and validate the first protein-based sensors for quantifying ionic strength in living cells.
  • To enable spatiotemporal monitoring of ionic strength dynamics at the single-cell level.

Main Methods:

  • Protein engineering of Förster resonance energy transfer (FRET) based probes.
  • Utilizing FRET technology to detect changes in ionic strength.
  • Single-cell imaging and analysis.

Main Results:

  • Successful design and implementation of FRET-based protein sensors capable of measuring ionic strength.
  • Demonstration of the probes' ability to track ionic strength changes within individual cells over time.
  • Validation of the sensor's sensitivity and specificity for intracellular ionic conditions.

Conclusions:

  • The developed FRET protein sensors represent a significant advancement in measuring intracellular ionic strength.
  • This technology provides unprecedented insights into cellular biochemistry and the behavior of biomacromolecules.
  • Future applications include studying various cellular processes influenced by ionic strength fluctuations.