Related Experiment Video
Updated: Mar 9, 2026

Use of Capillary Electrophoresis Immunoassay to Search for Potential Biomarkers of Amyotrophic Lateral Sclerosis in Human Platelets
Published on: February 10, 2020
Comparison of three methods for analyzing loureirin B and human serum albumin interaction using capillary
Yuelin Zhang1, Yijie Sha1, Kai Qian2
1Shanghai Key Lab Bioenergy Crops, School of Life Sciences, Shanghai University, Shanghai, P. R. China.
Abstract:
Loureirin B (LB), a bioactive drug, is widely used in the treatment of biological diseases. However, due to its poor solution in water, it is important to find the approach which helps LB to specific biological targets. As the most abundant protein in plasma, HSA plays the role of a carrier of numerous drug ligand. Thus, the interaction between LB and HSA was explored by ACE, CE frontal analysis, and pressure-mediated ACE under simulated physiological conditions (pH 7.4). The binding constants were calculated as 13.14 × 104 L/mol, 7.00 × 104 L/mol, and 2.78 × 104 L/mol for each method, respectively. At the same time, the binding site number (n = 1.429) could be only calculated by the CE frontal analysis method. Furthermore, good experimental repeatability was obtained by pressure-mediated ACE with RSDs for retention times and peak areas within 2.149 and 1.228, respectively.
More Related Videos
Related Concept Videos
Capillary Electrophoresis: Applications
Capillary zone electrophoresis (CZE) separates ionic components based on their electrophoretic mobility. It has been used to separate proteins, amino acids,...
Electrophoresis: Overview
There...
Capillary Electrophoresis: Instrumentation
Protein-Drug Binding: Determination Methods
Indirect methods involve isolating the bound drug from its free form in biological samples such as blood, serum, or plasma. These techniques aim to measure the percentage of drugs bound to proteins. Equilibrium dialysis is a commonly used method where the free drug concentration at equilibrium is measured by separating the bound...

