| Literature DB >> 30426411 |
Hiroyuki Matsumoto1,2, Hisao Haniu3, Naoka Komori4.
Abstract
An apparent molecular weight (MW) of a protein can be determined from the migration distance of a protein complexed with a strong cationic detergent sodium dodecyl sulfate (SDS) separated on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). This method was established around 1969 and has been utilized substantially even today because of its simplicity. During the following half a century, although it has been reported that many proteins show some deviation in MW when determined on SDS-PAGE especially when their peptide chains are posttranslationally modified, this versatile method is still being used very often in current biochemical works. In this protocol, a simple method to estimate MW by running SDS-PAGE of standard proteins is explained by an example in which proteins extracted from mouse retina were analyzed by two-dimensional isoelectric focusing (2-D IEF) SDS-PAGE followed by protein identification by peptide mass fingerprinting.Entities:
Keywords: 2-D gel; Protein identification by mass spectrometry; Protein molecular weight (MW); SDS-PAGE
Mesh:
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Year: 2019 PMID: 30426411 DOI: 10.1007/978-1-4939-8793-1_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745