1992
DOI: 10.1042/bj2830209
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Separation, purification and N-terminal sequence analysis of a novel leupeptin-sensitive serine endopeptidase present in chemically induced rat mammary tumour

Abstract: Leupeptin is a small peptide microbially derived inhibitor of certain proteolytic enzymes. Using N-alpha-benzoyl-DL-arginine 4-nitroanilide as substrate, we found a novel leupeptin-sensitive proteolytic enzyme in N-methyl-N-nitrosourea(MNU)-induced rat mammary adenocarcinoma. This enzyme was apparently different from urokinase-type plasminogen activator or cathepsin B and was present in mammary tumour at levels at least 20 times higher than those in normal mammary tissue. This enzyme was separated and purified… Show more

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Cited by 5 publications
(1 citation statement)
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“…We have partially purified the enzyme from breasttumour tissue using a benzamidine-sepharose affinity column, and have compared its inhibitor susceptibility to that of rat mast cell tryptase which, in a recent report by Eto and Grubbs [3], was found to be produced in chemically induced rat mammary tumours. The results are summarised in table 2.…”
Section: Rangementioning
confidence: 98%
“…We have partially purified the enzyme from breasttumour tissue using a benzamidine-sepharose affinity column, and have compared its inhibitor susceptibility to that of rat mast cell tryptase which, in a recent report by Eto and Grubbs [3], was found to be produced in chemically induced rat mammary tumours. The results are summarised in table 2.…”
Section: Rangementioning
confidence: 98%