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An ultrafiltration assay for lysyl oxidase.

Authors :
Shackleton DR
Hulmes DJ
Source :
Analytical biochemistry [Anal Biochem] 1990 Mar; Vol. 185 (2), pp. 359-62.
Publication Year :
1990

Abstract

A modification of the original microdistillation assay for lysyl oxidase is described in which Amicon C-10 microconcentrators are used to separate, by ultrafiltration, the 3H-labeled products released from a [4,5-3H]-lysine-labeled elastin substrate. Enzyme activity is determined by scintillation counting of the ultrafiltrate, after subtraction of radioactivity released in the presence of beta-aminopropionitrile, a specific inhibitor of the enzyme. Conditions are described which optimize both the sensitivity and the efficient use of substrate. The assay shows linear inhibition of activity in up to 1 M urea; hence, as the enzyme is normally diluted in the assay, samples in 6 M urea can be assayed directly, without prior dialysis, and corrected for partial inhibition. Comparable results are obtained when enzyme activity is assayed by ultrafiltration or microdistillation. The assay is simple and convenient and, by using disposable containers throughout, it eliminates the need for time-consuming decontamination of radioactive glassware.

Details

Language :
English
ISSN :
0003-2697
Volume :
185
Issue :
2
Database :
MEDLINE
Journal :
Analytical biochemistry
Publication Type :
Academic Journal
Accession number :
1971160
Full Text :
https://doi.org/10.1016/0003-2697(90)90308-v