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PMID: 3543004 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Human pituitary tryptase: molecular forms, NH2-terminal sequence, immunocytochemical localization, and specificity with prohormone and fluorogenic substrates.

The Journal of biological chemistry ·Vol. 262 ·No. 3 ·1987-01-25 ·Pages 1363-73

Cromlish JA, Seidah NG, Marcinkiewicz M, Hamelin J, Johnson DA, Chrétien M

Abstract

A human pituitary-derived serine protease, immunologically identical to human lung tryptase (Smith, T. J., Hougland, M.W., and Johnson, D.A. (1984) J. Biol. Chem. 259, 11046-11051), was found immunohistochemically to be associated with mast cells present in pituitary connective tissue. Western blotting combined with sodium dodecyl sulfate-polyacrylamide gel electrophoresis indicated the presence of multiple forms: a major Mr 36,300 form and three minor forms with Mr 32,400, 33,400, and 34,600. Two major forms with Mr 35,600 and 34,100 were detected by affinity labeling with 125I-D-Tyr-Glu-Phe-Lys-Arg-CH2Cl. Treatment of the pituitary tryptase preparation with N-glycosidase F indicated that some of the molecular weight heterogeneity results from N-linked glycosylation. The multiple molecular weight forms appear to have the same NH2-terminal sequence: Ile-Val-Gly-Gly-Gln-Glu-Ala-Pro. Pituitary tryptase has an apparent Mr = 110,000 by gel filtration on Sephadex G-200 in the presence of 0.3 M NaCl, indicating that the enzyme may be a tetramer of Mr = 32,400-36,300 subunits. However, this quaternary structure was not stable to gradient polyacrylamide gel electrophoresis. Human pituitary tryptase was so reactive toward synthetic tripeptide coumarin-containing substrates containing a pair of basic amino acids at the site of cleavage such as benzyloxylcarbonyl-L-Ala-L-Lys-L-Arg-4-methylcoumarin-7-amide (k cat/Km = 2.38 X 10(8) M-1 s-1) that Briggs-Haldane kinetics may apply. The reversible inhibitor NaCl at a concentration of 1 M decreased the k cat/Km for benzyloxylcarbonyl-L-Ala-L-Lys-L-Arg-4-methylcoumarin-7-amide to 6.53 X 10(6) M-1 s-1, which reflected a 100-fold increase in apparent Km. Based on active site titration with fluorescein mono-p-guanidinobenzoate hydrochloride, NaCl had no effect on the number of accessible active sites. Substrate specificity studies with prohormones indicated that pituitary tryptase has a preference for cleaving COOH-terminal to arginine or lysine residues which are preceded by a proline residue 4 or 6 residues NH2-terminal to the site of cleavage.

MeSH Terms
Amino Acid Sequence Binding Sites Coumarins/metabolism Electrophoresis, Polyacrylamide Gel Fluoresceins/metabolism Fluorescent Dyes Histocytochemistry Humans Hydrogen-Ion Concentration Immunologic Tests Kinetics Lung/enzymology Macromolecular Substances Mast Cells/enzymology Molecular Weight Peptide Fragments Peptide Hydrolases/analysis,metabolism Pituitary Gland/enzymology Protein Precursors/metabolism Sodium Chloride/pharmacology Substrate Specificity
Chemicals
Coumarins Fluoresceins Fluorescent Dyes Macromolecular Substances Peptide Fragments Protein Precursors Sodium Chloride fluorescein mono-p-guanidinobenzoate Peptide Hydrolases tosylarginine methyl ester hydrolase 7-amino-4-methylcoumarin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Cromlish J A
Seidah N G
Marcinkiewicz M
Hamelin J
Johnson D A
Chrétien M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1987-01-25
Pages
1363-73
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NINDS NIH HHS · 5RO1-NS16315-06 · United States
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