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

The Equilibrium Binding Constant and Binding Strength02:18

The Equilibrium Binding Constant and Binding Strength

14.9K
The equilibrium binding constant (Kb) quantifies the strength of a protein-ligand interaction. Kb can be calculated as follows when the reaction is at equilibrium:
14.9K
The Equilibrium Binding Constant and Binding Strength02:18

The Equilibrium Binding Constant and Binding Strength

10.0K
10.0K
Seedless Vascular Plants03:24

Seedless Vascular Plants

66.7K
Seedless Vascular Plants Were the First Tall Plants on Earth
66.7K
Ligand Binding Sites02:40

Ligand Binding Sites

14.9K
Proteins are dynamic macromolecules that carry out a wide variety of essential processes; however, the activities of most proteins depend on their interactions with other molecules or ions, known as ligands.
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
14.9K
Conserved Binding Sites01:49

Conserved Binding Sites

5.1K
Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
5.1K
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

5.5K
Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence...
5.5K

You might also read

Related Articles

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

Sort by
Same author

Collecting Duct-Targeted Lipid Nanoparticles Deliver <i>Pkd2</i> mRNA to Restore Polycystin-2 and Attenuate ADPKD.

bioRxiv : the preprint server for biology·2026
Same author

Investigation of Urinary Extracellular Vesicles as Novel and Safe Therapeutics for Autosomal Recessive Polycystic Kidney Disease (ARPKD).

Journal of biomedical materials research. Part A·2026
Same author

Bioengineering and nephrology converge to drive kidney-targeted therapies.

Nature reviews. Nephrology·2025
Same author

Genetically engineering cells to produce therapeutically boosted extracellular vesicles for cardiovascular calcification.

Biomaterials·2025
Same author

Clinically relevant dosing of miR-145 micelles curbs atherosclerosis in vivo.

Journal of controlled release : official journal of the Controlled Release Society·2025
Same author

Targeting Dysregulated Epigenetic Modifiers With Kidney-Targeted Nanotherapeutics for Polycystic Kidney Disease.

Journal of biomedical materials research. Part A·2025

Related Experiment Video

Updated: Jan 24, 2026

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis
07:45

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis

Published on: February 9, 2021

4.0K

Calcium-binding nanoparticles for vascular disease.

Deborah D Chin1, Sampreeti Chowdhuri1, Eun Ji Chung1,2,3,4,5,6

  • 1Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, USA.

Regenerative Engineering and Translational Medicine
|May 21, 2019
PubMed
Summary

Cardiovascular disease (CVD) involves calcified plaques in blood vessels, increasing rupture risk. Novel nanoparticles offer advanced imaging to detect vascular calcification and plaque composition, improving diagnostics for atherosclerosis.

Keywords:
Cardiovascular diseaseDrug deliveryImagingNanoparticlePeptidesVascular calcification

More Related Videos

Assessment of Vascular Function in Patients With Chronic Kidney Disease
08:50

Assessment of Vascular Function in Patients With Chronic Kidney Disease

Published on: June 16, 2014

16.7K
Orthotopic Aortic Transplantation in Mice for the Study of Vascular Disease
09:06

Orthotopic Aortic Transplantation in Mice for the Study of Vascular Disease

Published on: November 28, 2012

11.4K

Related Experiment Videos

Last Updated: Jan 24, 2026

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis
07:45

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis

Published on: February 9, 2021

4.0K
Assessment of Vascular Function in Patients With Chronic Kidney Disease
08:50

Assessment of Vascular Function in Patients With Chronic Kidney Disease

Published on: June 16, 2014

16.7K
Orthotopic Aortic Transplantation in Mice for the Study of Vascular Disease
09:06

Orthotopic Aortic Transplantation in Mice for the Study of Vascular Disease

Published on: November 28, 2012

11.4K

Area of Science:

  • Biomedical Engineering
  • Cardiovascular Research
  • Nanotechnology

Background:

  • Cardiovascular disease (CVD) is a leading global cause of mortality.
  • Atherosclerosis involves plaque calcification, linked to plaque rupture and acute myocardial infarction.
  • Current imaging techniques for vascular calcification lack detail on plaque composition and structure.

Purpose of the Study:

  • To review the role of calcification in atherosclerosis and plaque instability.
  • To summarize current clinical methods for detecting vascular calcification.
  • To highlight the potential of nanoparticles for improved calcium detection.

Main Methods:

  • Literature review of calcification in atherosclerosis.
  • Analysis of current clinical imaging modalities.
  • Exploration of nanoparticle-based imaging strategies.

Main Results:

  • Vascular calcification is a critical factor in atherosclerotic plaque instability.
  • Existing imaging methods have limitations in assessing plaque composition.
  • Nanoparticles offer a versatile platform for targeted imaging agents.

Conclusions:

  • Nanoparticles can overcome limitations of current imaging methods for vascular calcification.
  • Calcium-targeting ligands and nanoparticles show promise for novel diagnostic tools.
  • Advanced nanoparticle-based imaging could improve the understanding and management of atherosclerosis.