Literature DB >> 18411270

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

Adam A Golabek1, Natalia Dolzhanskaya, Marius Walus, Krystyna E Wisniewski, Elizabeth Kida.   

Abstract

Tripeptidyl peptidase I (TPP I) is the first mammalian representative of a family of pepstatin-insensitive serine-carboxyl proteases, or sedolisins. The enzyme acts in lysosomes, where it sequentially removes tripeptides from the unmodified N terminus of small, unstructured polypeptides. Naturally occurring mutations in TPP I underlie a neurodegenerative disorder of childhood, classic late infantile neuronal ceroid lipofuscinosis (CLN2). Generation of mature TPP I is associated with removal of a long prosegment of 176 amino acid residues from the zymogen. Here we investigated the inhibitory properties of TPP I prosegment expressed and isolated from Escherichia coli toward its cognate protease. We show that the TPP I prosegment is a potent, slow-binding inhibitor of its parent enzyme, with an overall inhibition constant in the low nanomolar range. We also demonstrate the protective effect of the prosegment on alkaline pH-induced inactivation of the enzyme. Interestingly, the inhibitory properties of TPP I prosegment with the introduced classic late infantile neuronal ceroid lipofuscinosis disease-associated mutation, G77R, significantly differed from those revealed by wild-type prosegment in both the mechanism of interaction and the inhibitory rate. This is the first characterization of the inhibitory action of the sedolisin prosegment.

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Year:  2008        PMID: 18411270      PMCID: PMC2423245          DOI: 10.1074/jbc.M800458200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  38 in total

1.  The prosegments of furin and PC7 as potent inhibitors of proprotein convertases. In vitro and ex vivo assessment of their efficacy and selectivity.

Authors:  M Zhong; J S Munzer; A Basak; S Benjannet; S J Mowla; E Decroly; M Chrétien; N G Seidah
Journal:  J Biol Chem       Date:  1999-11-26       Impact factor: 5.157

2.  Mechanism of Kex2p inhibition by its proregion.

Authors:  G Lesage; M Tremblay; J Guimond; G Boileau
Journal:  FEBS Lett       Date:  2001-11-23       Impact factor: 4.124

3.  Biosynthesis, glycosylation, and enzymatic processing in vivo of human tripeptidyl-peptidase I.

Authors:  Adam A Golabek; Elizabeth Kida; Marius Walus; Peter Wujek; Pankaj Mehta; Krystyna E Wisniewski
Journal:  J Biol Chem       Date:  2002-12-17       Impact factor: 5.157

Review 4.  Tripeptidyl-peptidase I in health and disease.

Authors:  Adam A Golabek; Elizabeth Kida
Journal:  Biol Chem       Date:  2006-08       Impact factor: 3.915

5.  Distribution of tripeptidyl peptidase I in human tissues under normal and pathological conditions.

Authors:  E Kida; A A Golabek; M Walus; P Wujek; W Kaczmarski; K E Wisniewski
Journal:  J Neuropathol Exp Neurol       Date:  2001-03       Impact factor: 3.685

6.  Production and characterization of recombinant human CLN2 protein for enzyme-replacement therapy in late infantile neuronal ceroid lipofuscinosis.

Authors:  L Lin; P Lobel
Journal:  Biochem J       Date:  2001-07-01       Impact factor: 3.857

7.  The human CLN2 protein/tripeptidyl-peptidase I is a serine protease that autoactivates at acidic pH.

Authors:  L Lin; I Sohar; H Lackland; P Lobel
Journal:  J Biol Chem       Date:  2000-10-27       Impact factor: 5.157

8.  A CLN2-related and thermostable serine-carboxyl proteinase, kumamolysin: cloning, expression, and identification of catalytic serine residue.

Authors:  Hiroshi Oyama; Takatoshi Hamada; Shin Ogasawara; Kenichi Uchida; Sawao Murao; Bret B Beyer; Ben M Dunn; Kohei Oda
Journal:  J Biochem       Date:  2002-05       Impact factor: 3.387

9.  Characterization of endopeptidase activity of tripeptidyl peptidase-I/CLN2 protein which is deficient in classical late infantile neuronal ceroid lipofuscinosis.

Authors:  J Ezaki; M Takeda-Ezaki; K Oda; E Kominami
Journal:  Biochem Biophys Res Commun       Date:  2000-02-24       Impact factor: 3.575

10.  Distribution and development of CLN2 protein, the late-infantile neuronal ceroid lipofuscinosis gene product.

Authors:  Y Kurachi; A Oka; M Itoh; M Mizuguchi; M Hayashi; S Takashima
Journal:  Acta Neuropathol       Date:  2001-07       Impact factor: 17.088

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  4 in total

1.  A critical tryptophan and Ca2+ in activation and catalysis of TPPI, the enzyme deficient in classic late-infantile neuronal ceroid lipofuscinosis.

Authors:  Salomon Kuizon; Kathleen DiMaiuta; Marius Walus; Edmund C Jenkins; Marisol Kuizon; Elizabeth Kida; Adam A Golabek; Daniel O Espinoza; Raju K Pullarkat; Mohammed A Junaid
Journal:  PLoS One       Date:  2010-08-03       Impact factor: 3.752

2.  Crystal structure and autoactivation pathway of the precursor form of human tripeptidyl-peptidase 1, the enzyme deficient in late infantile ceroid lipofuscinosis.

Authors:  Jayita Guhaniyogi; Istvan Sohar; Kalyan Das; Ann M Stock; Peter Lobel
Journal:  J Biol Chem       Date:  2008-11-26       Impact factor: 5.157

Review 3.  Interactions of the proteins of neuronal ceroid lipofuscinosis: clues to function.

Authors:  Amanda L Getty; David A Pearce
Journal:  Cell Mol Life Sci       Date:  2010-08-01       Impact factor: 9.207

4.  Structure-function analysis of Sedolisins: evolution of tripeptidyl peptidase and endopeptidase subfamilies in fungi.

Authors:  Facundo Orts; Arjen Ten Have
Journal:  BMC Bioinformatics       Date:  2018-12-04       Impact factor: 3.169

  4 in total

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