Related Experiment Video
Updated: May 13, 2025

Two-dimensional Gel Electrophoresis Coupled with Mass Spectrometry Methods for an Analysis of Human Pituitary Adenoma Tissue Proteome
Published on: April 2, 2018
What does one-dimensional gel electrophoresis-based western blotting data really mean in the reality of proteoforms?
Lamei Yang1, Qianwen Shao2, Juwen Su1
1Shandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer HospItal and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, 440 Jiyan Road, Jinan, Shandong, 250117, PR China.
Abstract:
One-dimensional gel electrophoresis-based western blotting (1DE-WB) is a routine technique for protein analysis. However, multiple immunoreactive bands are often found for a single protein target in 1DE-WB, yet only the band corresponding to the theoretical molecular weight of the canonical protein is considered relevant and additional immunoreactive bands are dismissed as false positives. However, what additional bands actually contain has not been established. Proteoforms are the final structural and functional entities of a gene product. Here, multiple immunopositive bands in the 1DE-WB analysis of growth hormone and prolactin in human pituitary tissue samples were identified by MS, 2DE-WB, or 2DE-WB combined with MS, and immunopositive bands were found to contain multiple proteoforms; a range of published 1DE-WB data indicate this is likely a common phenomenon. Thus, multiple 1DE-WB positive bands are likely to represent different proteoforms rather than non-specific reactions and MS, 2DE-WB, or 2DE-WB combined with MS are effective approaches to identify proteoforms and thus more thoroughly understand 1DE-WB data.
Related Concept Videos
Two-dimensional Gel Electrophoresis
The first dimension separation uses the isoelectric focusing or IEF technique performed on immobilized pH gradient (IPG) strips that separate proteins according to their isoelectric points.
Biological samples, such...
Western Blotting
The technique begins with separating proteins from the sample using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by protein transfer, immunoblotting, and finally, protein detection.
SDS-PAGE
A variation of gel electrophoresis, termed polyacrylamide gel electrophoresis (PAGE), is commonly used for separating proteins according to their molecular size by passing them through a polyacrylamide gel. Because of the varying charges associated with amino acid side chains, PAGE can be used to separate intact...
Electrophoresis: Overview
There...

