Literature DB >> 6364138

Synthesis of peptides related to the prosegment of mouse submaxillary gland renin precursor: an approach to renin inhibitors.

G Evin, J Devin, B Castro, J Menard, P Corvol.   

Abstract

The complete sequence of the structural gene coding for mouse submaxillary gland renin was recently reported and the amino acid sequence of preprorenin was deduced. This sequence includes a 45-amino acid peptide that corresponds to the prosegment of the renin precursor. To investigate whether peptides related to the renin prosegment are able to inhibit renin activity, we have synthesized four peptides having the following structures: Arg-Ile-Pro-OMe, butyloxycarbonyl(Boc)-Leu-Lys-Lys-Met-Pro-OMe, Boc-Arg-Ile-Pro-Leu-Lys-Lys-Met-Pro-OMe, and Boc-Glu-Arg-Ile-Pro-Leu-Lys-Lys-Met-Pro-OMe (corresponding to amino acids 12-14, 15-19, 12-19, and 11-19, respectively, of the renin prosegment). All four peptides were found to inhibit the activity of pure mouse submaxillary renin on a porcine synthetic tetra-decapeptide in vitro, and the most potent inhibitors exhibited IC50 values in the micromolar range. Enzymatic kinetic studies carried out using peptide 15-19 showed an uncompetitive or a mixed type of inhibition with a Ki value of 2.3 X 10(-6) M at 37 degrees C in 0.5 M citrate/phosphate buffer (pH 6.0).

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Year:  1984        PMID: 6364138      PMCID: PMC344607          DOI: 10.1073/pnas.81.1.48

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

1.  Inhibition of pepsin by zymogen activation fragments. Spectrum of peptides released from pepsinogen NH2 terminus and solid phase synthesis of two inhibitory peptide sequences.

Authors:  B M Dunn; C Deyrup; W G Moesching; W A Gilbert; R J Nolan; M L Trach
Journal:  J Biol Chem       Date:  1978-10-25       Impact factor: 5.157

2.  Complete amino acid sequence and maturation of the mouse submaxillary gland renin precursor.

Authors:  J J Panthier; S Foote; B Chambraud; A D Strosberg; P Corvol; F Rougeon
Journal:  Nature       Date:  1982-07-01       Impact factor: 49.962

3.  Primary structure of human pepsinogen gene.

Authors:  K Sogawa; Y Fujii-Kuriyama; Y Mizukami; Y Ichihara; K Takahashi
Journal:  J Biol Chem       Date:  1983-04-25       Impact factor: 5.157

4.  Potent new inhibitors of human renin.

Authors:  M Szelke; B Leckie; A Hallett; D M Jones; J Sueiras; B Atrash; A F Lever
Journal:  Nature       Date:  1982-10-07       Impact factor: 49.962

5.  Purification of a completely inactive renin from hog kidney and identification as renin zymogen.

Authors:  Y Takii; T Inagami
Journal:  Biochem Biophys Res Commun       Date:  1982-01-15       Impact factor: 3.575

6.  A substrate analog inhibitor of renin that is effective in vivo.

Authors:  R J Cody; J Burton; G Evin; K Poulsen; J A Herd; E Haber
Journal:  Biochem Biophys Res Commun       Date:  1980-11-17       Impact factor: 3.575

7.  Cathepsinogen D: characterization and activation to cathepsin D and inhibitory peptides.

Authors:  V Puizdar; V Turk
Journal:  FEBS Lett       Date:  1981-09-28       Impact factor: 4.124

8.  The nature of renin precursor and inactive renin.

Authors:  V J Dzau; A Tanaka; R E Pratt
Journal:  Clin Exp Hypertens A       Date:  1982

9.  Novel renin inhibitors containing the amino acid statine.

Authors:  J Boger; N S Lohr; E H Ulm; M Poe; E H Blaine; G M Fanelli; T Y Lin; L S Payne; T W Schorn; B I LaMont; T C Vassil; I I Stabilito; D F Veber; D H Rich; A S Bopari
Journal:  Nature       Date:  1983 May 5-11       Impact factor: 49.962

10.  New renin inhibitors homologous with pepstatin.

Authors:  M Eid; G Evin; B Castro; J Menard; P Corvol
Journal:  Biochem J       Date:  1981-08-01       Impact factor: 3.857

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  3 in total

1.  Analysis by immunocytochemistry and in situ hybridization of renin and its mRNA in kidney, testis, adrenal, and pituitary of the rat.

Authors:  C F Deschepper; S H Mellon; F Cumin; J D Baxter; W F Ganong
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

2.  Two distinct gene subfamilies within the family of cysteine protease genes.

Authors:  K M Karrer; S L Peiffer; M E DiTomas
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-01       Impact factor: 11.205

3.  Prosegment of tripeptidyl peptidase I is a potent, slow-binding inhibitor of its cognate enzyme.

Authors:  Adam A Golabek; Natalia Dolzhanskaya; Marius Walus; Krystyna E Wisniewski; Elizabeth Kida
Journal:  J Biol Chem       Date:  2008-04-14       Impact factor: 5.157

  3 in total

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