Prolyl Oligopeptidase from the Blood Fluke Schistosoma mansoni: From Functional Analysis to Anti-schistosomal Inhibitors

. 2015 ; 9 (6) : e0003827. [epub] 20150603

Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid26039195

BACKGROUND: Blood flukes of the genus Schistosoma cause schistosomiasis, a parasitic disease that infects over 240 million people worldwide, and for which there is a need to identify new targets for chemotherapeutic interventions. Our research is focused on Schistosoma mansoni prolyl oligopeptidase (SmPOP) from the serine peptidase family S9, which has not been investigated in detail in trematodes. METHODOLOGY/PRINCIPAL FINDINGS: We demonstrate that SmPOP is expressed in adult worms and schistosomula in an enzymatically active form. By immunofluorescence microscopy, SmPOP is localized in the tegument and parenchyma of both developmental stages. Recombinant SmPOP was produced in Escherichia coli and its active site specificity investigated using synthetic substrate and inhibitor libraries, and by homology modeling. SmPOP is a true oligopeptidase that hydrolyzes peptide (but not protein) substrates with a strict specificity for Pro at P1. The inhibition profile is analogous to those for mammalian POPs. Both the recombinant enzyme and live worms cleave host vasoregulatory, proline-containing hormones such as angiotensin I and bradykinin. Finally, we designed nanomolar inhibitors of SmPOP that induce deleterious phenotypes in cultured schistosomes. CONCLUSIONS/SIGNIFICANCE: We provide the first localization and functional analysis of SmPOP together with chemical tools for measuring its activity. We briefly discuss the notion that SmPOP, operating at the host-parasite interface to cleave host bioactive peptides, may contribute to the survival of the parasite. If substantiated, SmPOP could be a new target for the development of anti-schistosomal drugs.

Zobrazit více v PubMed

Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J (2006) Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect Dis 6: 411–425. S1473-3099(06)70521-7. PubMed

Lockyer AE, Olson PD, Ostergaard P, Rollinson D, Johnston DA, et al. (2003) The phylogeny of the Schistosomatidae based on three genes with emphasis on the interrelationships of Schistosoma Weinland, 1858. Parasitology 126: 203–224. PubMed

Gryseels B, Polman K, Clerinx J, Kestens L (2006) Human schistosomiasis. Lancet 368: 1106–1118. PubMed

Burke ML, Jones MK, Gobert GN, Li YS, Ellis MK, et al. (2009) Immunopathogenesis of human schistosomiasis. Parasite Immunol 31: 163–176. 10.1111/j.1365-3024.2009.01098.x PubMed DOI

Crum NF, Chun HM, Favata MA, Hale BR (2003) Gastrointestinal Schistosomiasis japonicum infections in immigrants from the Island of Leyte, Philippines. J Travel Med 10: 131–132. PubMed

Caffrey CR (2007) Chemotherapy of schistosomiasis: present and future. Curr Opin Chem Biol 11: 433–439. PubMed

Melman SD, Steinauer ML, Cunningham C, Kubatko LS, Mwangi IN, et al. (2009) Reduced susceptibility to praziquantel among naturally occurring Kenyan isolates of Schistosoma mansoni . PLoS Negl Trop Dis 3: e504 10.1371/journal.pntd.0000504 PubMed DOI PMC

Abdulla MH, Ruelas DS, Wolff B, Snedecor J, Lim KC, et al. (2009) Drug discovery for schistosomiasis: hit and lead compounds identified in a library of known drugs by medium-throughput phenotypic screening. PLoS Negl Trop Dis 3: e478 10.1371/journal.pntd.0000478 PubMed DOI PMC

Abdulla MH, Lim KC, Sajid M, McKerrow JH, Caffrey CR (2007) Schistosomiasis mansoni: novel chemotherapy using a cysteine protease inhibitor. PLoS Med 4: e14 PubMed PMC

Sajid M, McKerrow JH (2002) Cysteine proteases of parasitic organisms. Mol Biochem Parasitol 120: 1–21. PubMed

McKerrow JH, Caffrey C, Kelly B, Loke P, Sajid M (2006) Proteases in parasitic diseases. Annu Rev Pathol 1: 497–536. PubMed

Berriman M, Haas BJ, LoVerde PT, Wilson RA, Dillon GP, et al. (2009) The genome of the blood fluke Schistosoma mansoni . Nature 460: 352–358. 10.1038/nature08160 PubMed DOI PMC

Ingram JR, Rafi SB, Eroy-Reveles AA, Ray M, Lambeth L, et al. (2012) Investigation of the proteolytic functions of an expanded cercarial elastase gene family in Schistosoma mansoni . PLoS Negl Trop Dis 6: e1589 10.1371/journal.pntd.0001589 PubMed DOI PMC

Delcroix M, Sajid M, Caffrey CR, Lim KC, Dvorak J, et al. (2006) A multienzyme network functions in intestinal protein digestion by a platyhelminth parasite. J Biol Chem 281: 39316–39329. PubMed

Caffrey CR, McKerrow JH, Salter JP, Sajid M (2004) Blood 'n' guts: an update on schistosome digestive peptidases. Trends Parasitol 20: 241–248. PubMed

Jilkova A, Rezacova P, Lepsik M, Horn M, Vachova J, et al. (2011) Structural basis for inhibition of cathepsin B drug target from the human blood fluke, Schistosoma mansoni . J Biol Chem 286: 35770–35781. 10.1074/jbc.M111.271304 PubMed DOI PMC

Horn M, Jilkova A, Vondrasek J, Maresova L, Caffrey CR, et al. (2011) Mapping the pro-peptide of the Schistosoma mansoni cathepsin B1 drug target: modulation of inhibition by heparin and design of mimetic inhibitors. ACS Chem Biol 6: 609–617. 10.1021/cb100411v PubMed DOI

Fanfrlik J, Brahmkshatriya PS, Rezac J, Jilkova A, Horn M, et al. (2013) Quantum mechanics-based scoring rationalizes the irreversible inactivation of parasitic Schistosoma mansoni cysteine peptidase by vinyl sulfone inhibitors. J Phys Chem B 117: 14973–14982. 10.1021/jp409604n PubMed DOI

Jilkova A, Horn M, Rezacova P, Maresova L, Fajtova P, et al. (2014) Activation route of the Schistosoma mansoni cathepsin B1 drug target: structural map with a glycosaminoglycan switch. Structure 22: 1786–1798. 10.1016/j.str.2014.09.015 PubMed DOI

Rawlings ND, Waller M, Barrett AJ, Bateman A (2014) MEROPS: the database of proteolytic enzymes, their substrates and inhibitors. Nucleic Acids Res 42: D503–D509. 10.1093/nar/gkt953 PubMed DOI PMC

Szeltner Z, Polgar L (2008) Structure, function and biological relevance of prolyl oligopeptidase. Curr Protein Pept Sci 9: 96–107. PubMed

Grellier P, Vendeville S, Joyeau R, Bastos IM, Drobecq H, et al. (2001) Trypanosoma cruzi prolyl oligopeptidase Tc80 is involved in nonphagocytic mammalian cell invasion by trypomastigotes. J Biol Chem 276: 47078–47086. PubMed

Bastos IM, Grellier P, Martins NF, Cadavid-Restrepo G, de Souza-Ault MR, et al. (2005) Molecular, functional and structural properties of the prolyl oligopeptidase of Trypanosoma cruzi (POP Tc80), which is required for parasite entry into mammalian cells. Biochem J 388: 29–38. PubMed PMC

Bastos IM, Motta FN, Grellier P, Santana JM (2013) Parasite prolyl oligopeptidases and the challenge of designing chemotherapeuticals for Chagas disease, leishmaniasis and African trypanosomiasis. Curr Med Chem 20: 3103–3115. PubMed PMC

Horn M, Fajtova P, Rojo AL, Ulrychova L, Bartosova-Sojkova P, et al. (2014) Trypsin- and Chymotrypsin-Like Serine Proteases in Schistosoma mansoni—'The Undiscovered Country'. PLoS Negl Trop Dis 8: e2766 10.1371/journal.pntd.0002766 PubMed DOI PMC

Stefanic S, Dvorak J, Horn M, Braschi S, Sojka D, et al. (2010) RNA interference in Schistosoma mansoni schistosomula: selectivity, sensitivity and operation for larger-scale screening. PLoS Negl Trop Dis 4: e850 10.1371/journal.pntd.0000850 PubMed DOI PMC

Colley DG, Wikel SK (1974) Schistosoma mansoni: simplified method for the production of schistosomules. Exp Parasitol 35: 44–51. PubMed

Basch PF (1981) Cultivation of Schistosoma mansoni in vitro. I. Establishment of cultures from cercariae and development until pairing. J Parasitol 67: 179–185. PubMed

Le TH, Blair D, Agatsuma T, Humair PF, Campbell NJ, et al. (2000) Phylogenies inferred from mitochondrial gene orders-a cautionary tale from the parasitic flatworms. Mol Biol Evol 17: 1123–1125. PubMed

Consortium SjGSaFA (2009) The Schistosoma japonicum genome reveals features of host-parasite interplay. Nature 460: 345–351. 10.1038/nature08140 PubMed DOI PMC

Young ND, Jex AR, Li B, Liu S, Yang L, et al. (2012) Whole-genome sequence of Schistosoma haematobium. Nat Genet 44: 221–225. 10.1038/ng.1065 PubMed DOI

Doleckova-Maresova L, Pavlik M, Horn M, Mares M (2005) De novo design of alpha-amylase inhibitor: a small linear mimetic of macromolecular proteinaceous ligands. Chem Biol 12: 1349–1357. PubMed

Maly DJ, Leonetti F, Backes BJ, Dauber DS, Harris JL, et al. (2002) Expedient solid-phase synthesis of fluorogenic protease substrates using the 7-amino-4-carbamoylmethylcoumarin (ACC) fluorophore. J Org Chem 67: 910–915. PubMed

Powers JC, Wilcox PE (1970) Design and synthesis of inhibitors for crystallographic studies on the active site of chymotrypsin. J Am Chem Soc 92: 1782–1783. PubMed

Ede NJ, Eagle SN, Wickham G, Bray AM, Warne B, et al. (2000) Solid phase synthesis of peptide aldehyde protease inhibitors. Probing the proteolytic sites of hepatitis C virus polyprotein. J Pept Sci 6: 11–18. PubMed

Caffrey CR, Ruppel A (1997) Cathepsin B-like activity predominates over cathepsin L-like activity in adult Schistosoma mansoni and S. japonicum . Parasitol Res 83: 632–635. PubMed

Labute P (2008) The generalized Born/volume integral implicit solvent model: estimation of the free energy of hydration using London dispersion instead of atomic surface area. J Comput Chem 29: 1693–1698. 10.1002/jcc.20933 PubMed DOI

Protasio AV, Tsai IJ, Babbage A, Nichol S, Hunt M, et al. (2012) A systematically improved high quality genome and transcriptome of the human blood fluke Schistosoma mansoni . PLoS Negl Trop Dis 6: e1455 10.1371/journal.pntd.0001455 PubMed DOI PMC

Cunningham DF, O'Connor B (1997) Proline specific peptidases. Biochim Biophys Acta 1343: 160–186. PubMed

Yoshimoto T, Kawahara K, Matsubara F, Kado K, Tsuru D (1985) Comparison of inhibitory effects of prolinal-containing peptide derivatives on prolyl endopeptidases from bovine brain and Flavobacterium. J Biochem 98: 975–979. PubMed

Garcia-Horsman JA, Mannisto PT, Venalainen JI (2007) On the role of prolyl oligopeptidase in health and disease. Neuropeptides 41: 1–24. PubMed

Wilk S (1983) Prolyl endopeptidase. Life Sci 33: 2149–2157. PubMed

Nakajima T, Ono Y, Kato A, Maeda J, Ohe T (1992) Y-29794—a non-peptide prolyl endopeptidase inhibitor that can penetrate into the brain. Neurosci Lett 141: 156–160. PubMed

Lawandi J, Gerber-Lemaire S, Juillerat-Jeanneret L, Moitessier N (2010) Inhibitors of prolyl oligopeptidases for the therapy of human diseases: defining diseases and inhibitors. J Med Chem 53: 3423–3438. 10.1021/jm901104g PubMed DOI

Polgar L (2002) The prolyl oligopeptidase family. Cell Mol Life Sci 59: 349–362. PubMed PMC

Ollis DL, Cheah E, Cygler M, Dijkstra B, Frolow F, et al. (1992) The alpha/beta hydrolase fold. Protein Eng 5: 197–211. PubMed

Nardini M, Dijkstra BW (1999) Alpha/beta hydrolase fold enzymes: the family keeps growing. Curr Opin Struct Biol 9: 732–737. PubMed

Fulop V, Bocskei Z, Polgar L (1998) Prolyl oligopeptidase: an unusual beta-propeller domain regulates proteolysis. Cell 94: 161–170. PubMed

Schonlein C, Heins J, Barth A (1990) Purification and characterization of prolyl endopeptidase from pig brain. Biol Chem Hoppe Seyler 371: 1159–1164. PubMed

Sharma KK, Ortwerth BJ (1994) Purification and characterization of prolyl oligopeptidase from bovine lens. Exp Eye Res 59: 107–115. PubMed

Bastos IM, Motta FN, Charneau S, Santana JM, Dubost L, Augustyns K, Grellier P (2010) Prolyl oligopeptidase of Trypanosoma brucei hydrolyzes native collagen, peptide hormones and is active in the plasma of infected mice. Microbes Infect 12: 457–466. 10.1016/j.micinf.2010.02.007 PubMed DOI

Caffrey CR, Salter JP, Lucas KD, Khiem D, Hsieh I, et al. (2002) SmCB2, a novel tegumental cathepsin B from adult Schistosoma mansoni. Mol Biochem Parasitol 121: 49–61. PubMed

Campbell DJ (2003) The renin-angiotensin and the kallikrein-kinin systems. Int J Biochem Cell Biol 35: 784–791. PubMed

Izumi Y, Iwao H (2006) Angiotensin II and Its Related Peptides. In: Katin AJ, editor. Handbook of Biologically Active Peptides, pp. 1169–1174.

Gallagher PE, Arter AL, Krishnan B, Garcia-Espinosa MA, Tallant A (2013) Angiotensin II/Angiotensin-(1–7). In: Katin AJ, editor. Handbook of Biologically Active Peptides. pp. 494–501.

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Nature-Inspired Gallinamides Are Potent Antischistosomal Agents: Inhibition of the Cathepsin B1 Protease Target and Binding Mode Analysis

. 2024 Jun 14 ; 10 (6) : 1935-1948. [epub] 20240517

Uncovering the essential roles of glutamate carboxypeptidase 2 orthologs in Caenorhabditis elegans

. 2024 Jan 31 ; 44 (1) : .

An evolutionary molecular adaptation of an unusual stefin from the liver fluke Fasciola hepatica redefines the cystatin superfamily

. 2023 Mar ; 299 (3) : 102970. [epub] 20230201

Spatial expression pattern of serine proteases in the blood fluke Schistosoma mansoni determined by fluorescence RNA in situ hybridization

. 2021 May 22 ; 14 (1) : 274. [epub] 20210522

Druggable Hot Spots in the Schistosomiasis Cathepsin B1 Target Identified by Functional and Binding Mode Analysis of Potent Vinyl Sulfone Inhibitors

. 2021 May 14 ; 7 (5) : 1077-1088. [epub] 20201111

Azanitrile Inhibitors of the SmCB1 Protease Target Are Lethal to Schistosoma mansoni: Structural and Mechanistic Insights into Chemotype Reactivity

. 2021 Jan 08 ; 7 (1) : 189-201. [epub] 20201210

Laser capture microdissection in combination with mass spectrometry: Approach to characterization of tissue-specific proteomes of Eudiplozoon nipponicum (Monogenea, Polyopisthocotylea)

. 2020 ; 15 (6) : e0231681. [epub] 20200617

SmSP2: A serine protease secreted by the blood fluke pathogen Schistosoma mansoni with anti-hemostatic properties

. 2018 Apr ; 12 (4) : e0006446. [epub] 20180420

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...