Abstract
A general method for detecting protease activities on acrylamide or agarose gels after sodium dodecyl sulfate - polyacrylamide gel electrophoresis (SDS-PAGE) using specific aminoacyl p-nitroanilide (NA) or peptidyl NA as substrate is described. This method is extended from the spectrophotometric assay of p-nitroaniline, which is a chromogenic product liberated by protease action on aminoacyl NA or peptidyl NA. The acrylamide gel containing protein bands was dipped directly into a solution which contained specific synthetic aminoacyl NA or peptidyl NA as a substrate or had been overlaid with an agarose gel containing the same substrate. The p- nitroaniline released on the acrylamide or agarose get by the specific protease was diazotized with sodium nitrite and then coupled to N-(1- naphthyl)-ethylenediamine to produce distinct activity band(s). The substrates used for protease activity staining on gels were identical to those used for spectrophotometric assays. Some applications are described.
Original language | English |
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Pages (from-to) | 486-490 |
Number of pages | 5 |
Journal | Electrophoresis |
Volume | 20 |
Issue number | 3 |
Publication status | Published - 1999 |
Externally published | Yes |
Keywords
- Activity staining
- p-Nitroanilide
- Protease
- Sodium dodecyl sulfate - polyacrylamide gel electrophoresis
ASJC Scopus subject areas
- Clinical Biochemistry