Literature DB >> 6420632

A sensitive radiometric assay for enkephalin convertase and other carboxypeptidase B-like enzymes.

G Stack, L D Fricker, S H Snyder.   

Abstract

A sensitive radiometric assay for carboxypeptidase B-like enzymes has been developed using enkephalin convertase, an enkephalin synthesizing carboxypeptidase. The assay is based on the differential solubility of 3H-labeled substrate and product in chloroform. The substrates 3H-benzoyl-Phe-Ala-Arg or 3H-benzoyl-Phe-Leu-Arg are poorly soluble in chloroform due to the charged arginine. The products of carboxypeptidase B-like activity on these substrates, 3H-benzoyl-Phe-Ala or 3H-benzoyl Phe-Leu partition quantitatively into chloroform, allowing rapid separation of product from substrate. This assay is approximately 100 times more sensitive than a similar fluorometric assay utilizing dansyl-Phe-Ala-Arg as a substrate.

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Year:  1984        PMID: 6420632     DOI: 10.1016/0024-3205(84)90581-2

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  3 in total

1.  Processing and secretion of human carboxypeptidase E by C6 glioma cells.

Authors:  E Manser; D Fernandez; L Lim
Journal:  Biochem J       Date:  1991-12-15       Impact factor: 3.857

Review 2.  Regulation of carboxypeptidase H by inhibitory and stimulatory mechanisms during neuropeptide precursor processing.

Authors:  V Y Hook
Journal:  Cell Mol Neurobiol       Date:  1988-03       Impact factor: 5.046

3.  Exocrine secretion granules contain peptide amidation activity.

Authors:  M von Zastrow; T R Tritton; J D Castle
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

  3 in total

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