Literature DB >> 3533059

The major excreted protein (MEP) of transformed mouse cells and cathepsin L have similar protease specificity.

S Gal, M M Gottesman.   

Abstract

The major excreted protein of transformed mouse cells is an acid activable cysteine protease. In this paper, oxidized insulin B chain is shown to be a substrate for this protease. By isolation and analysis of the insulin B peptides generated by the protease, the bond specificity of this protease was determined. The bonds preferentially cleaved are glu13-ala14, leu17-val18, and tyr26-thr27. No obvious preference for a specific amino acid was found in these studies. The bond specificity of this cysteine protease for oxidized insulin B chain has been compared with that of other proteases, and it is the same as that reported for cathepsin L, suggesting that the major excreted protein and cathepsin L may be the same protein.

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Year:  1986        PMID: 3533059     DOI: 10.1016/s0006-291x(86)80093-6

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  18 in total

1.  Characterization and expression of AmphiCL encoding cathepsin l proteinase from amphioxus Branchiostoma belcheri tsingtauense.

Authors:  Yongjun Wang; Shicui Zhang; Zhenhui Liu; Hongyan Li; Lei Wang
Journal:  Mar Biotechnol (NY)       Date:  2005 Jul-Aug       Impact factor: 3.619

2.  The application of a novel biotinylated affinity label for the detection of a cathepsin B-like precursor produced by breast-tumour cells in culture.

Authors:  B M Cullen; I M Halliday; G Kay; J Nelson; B Walker
Journal:  Biochem J       Date:  1992-04-15       Impact factor: 3.857

3.  Use of a cloned multidrug resistance gene for coamplification and overproduction of major excreted protein, a transformation-regulated secreted acid protease.

Authors:  S E Kane; B R Troen; S Gal; K Ueda; I Pastan; M M Gottesman
Journal:  Mol Cell Biol       Date:  1988-08       Impact factor: 4.272

4.  The major ras induced protein in NIH3T3 cells is cathepsin L.

Authors:  L Joseph; S Lapid; V Sukhatme
Journal:  Nucleic Acids Res       Date:  1987-04-10       Impact factor: 16.971

5.  Characterization of human cathepsin L promoter and identification of binding sites for NF-Y, Sp1 and Sp3 that are essential for its activity.

Authors:  Didier Jean; Nathalie Guillaume; Raymond Frade
Journal:  Biochem J       Date:  2002-01-01       Impact factor: 3.857

Review 6.  Reovirus receptors, cell entry, and proapoptotic signaling.

Authors:  Pranav Danthi; Geoffrey H Holm; Thilo Stehle; Terence S Dermody
Journal:  Adv Exp Med Biol       Date:  2013       Impact factor: 2.622

7.  Cloning and characterization of anti-cathepsin L single chain variable fragment whose expression inhibits procathepsin L secretion in human melanoma cells.

Authors:  Nathalie Guillaume-Rousselet; Didier Jean; Raymond Frade
Journal:  Biochem J       Date:  2002-10-01       Impact factor: 3.857

8.  Sequence and expression of the cDNA for MEP (major excreted protein), a transformation-regulated secreted cathepsin.

Authors:  B R Troen; S Gal; M M Gottesman
Journal:  Biochem J       Date:  1987-09-15       Impact factor: 3.857

9.  The N-terminal amino acid sequences of the heavy and light chains of human cathepsin L. Relationship to a cDNA clone for a major cysteine proteinase from a mouse macrophage cell line.

Authors:  R W Mason; J E Walker; F D Northrop
Journal:  Biochem J       Date:  1986-12-01       Impact factor: 3.857

10.  Isolation and sequence of a cDNA for human pro-(cathepsin L).

Authors:  S Gal; M M Gottesman
Journal:  Biochem J       Date:  1988-07-01       Impact factor: 3.857

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