Microplate assay for quantitative determination of cathepsin activities in viable cells using derivatives of 4-methoxy-beta-naphthylamide

A method is described allowing the selective determination of four cathepsins (B, H, K, and L) in live cells. Adherently growing cells are incubated with partially selective substrates for each cathepsin (peptidic derivatives of 4-methoxy-beta-naphthylamine) in microtiter plates together with nitros...

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Détails bibliographiques
Publié dans:BioTechniques. - 1993. - 41(2006), 4 vom: 27. Okt., Seite 469-73
Auteur principal: Rüttger, Anke (Auteur)
Autres auteurs: Mollenhauer, Jürgen, Löser, Reik, Gütschow, Michael, Wiederanders, Bernd
Format: Article
Langue:English
Publié: 2006
Accès à la collection:BioTechniques
Sujets:Comparative Study Journal Article Research Support, Non-U.S. Gov't Benzaldehydes Enzyme Inhibitors 5-nitrosalicylaldehyde 97-51-8 2-Naphthylamine CKR7XL41N4 Cathepsins plus... EC 3.4.- Aminopeptidases EC 3.4.11.- Cysteine Endopeptidases EC 3.4.22.- Cathepsin B EC 3.4.22.1 CTSL protein, human EC 3.4.22.15 Cathepsin L Ctsl protein, mouse CTSH protein, human EC 3.4.22.16 Cathepsin H Ctsh protein, mouse CTSK protein, human EC 3.4.22.38 Cathepsin K Ctsk protein, mouse Leucine GMW67QNF9C ubenimex I0J33N5627
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Résumé:A method is described allowing the selective determination of four cathepsins (B, H, K, and L) in live cells. Adherently growing cells are incubated with partially selective substrates for each cathepsin (peptidic derivatives of 4-methoxy-beta-naphthylamine) in microtiter plates together with nitrosalicylaldehyde. Using an appropriate reader accumulating fluorescent products may be detected continously or by end point measurement. Selectivity is achieved by running parallel assays containing inhibitors that are partially selective for each of the cathepsins (in case of cathepsin H, the nonlysosomal aminopeptidases are inhibited by bestatin). Individual cathepsin activities can then be calculated by the difference between the uninhibited and the inhibited assay. The method was validated by measurements in cells isolated from cathepsin B(-/-)-, K(-/-)-, and L(-/-)- mice. This strategy suggests that the combination of two partially selective reaction partners, substrate and inhibitor can yield selective cathepsin assays
Description:Date Completed 22.11.2006
Date Revised 16.08.2019
published: Print
Citation Status MEDLINE
ISSN:0736-6205