Literature DB >> 29151351

Immucillins in Infectious Diseases.

Gary B Evans1, Peter C Tyler1, Vern L Schramm2.   

Abstract

The Immucillins are chemically stable analogues that mimic the ribocation and leaving-group features of N-ribosyltransferase transition states. Infectious disease agents often rely on ribosyltransferase chemistry in pathways involving precursor synthesis for nucleic acids, salvage of nucleic acid precursors, or synthetic pathways with nucleoside intermediates. Here, we review three infectious agents and the use of the Immucillins to taget enzymes essential to the parasites. First, DADMe-Immucillin-G is a purine nucleoside phosphorylase (PNP) inhibitor that blocks purine salvage and shows clinical potential for treatment for the malaria parasite Plasmodium falciparum, a purine auxotroph requiring hypoxanthine for purine nucleotide synthesis. Inhibition of the PNPs in the host and in parasite cells leads to apurinic starvation and death. Second, Helicobacter pylori, a causative agent of human ulcers, synthesizes menaquinone, an essential electron transfer agent, in a pathway requiring aminofutalosine nucleoside hydrolysis. Inhibitors of the H. pylori methylthioadenosine nucleosidase (MTAN) are powerful antibiotics for this organism. Synthesis of menaquinone by the aminofutalosine pathway does not occur in most bacteria populating the human gut microbiome. Thus, MTAN inhibitors provide high-specificity antibiotics for H. pylori and are not expected to disrupt the normal gut bacterial flora. Third, Immucillin-A was designed as a transition state analogue of the atypical PNP from Trichomonas vaginalis. In antiviral screens, Immucillin-A was shown to act as a prodrug. It is active against filoviruses and flaviviruses. In virus-infected cells, Immucillin-A is converted to the triphosphate, is incorporated into the viral transcript, and functions as an atypical chain-terminator for RNA-dependent RNA polymerases. Immucillin-A has entered clinical trials for use as an antiviral. We also summarize other Immucillins that have been characterized in successful clinical trials for T-cell lymphoma and gout. The human trials support the potential development of the Immucillins in infectious diseases.

Entities:  

Keywords:  DADMe-Immucillin-G; Immucillin-A; RNA chain termination; RNA-dependent RNA polymerase; antivirals; futalosine pathway; malaria antibiotics; methylthioadenosine phosphorylase; purine nucleoside phosphorylase; purine-less death; species specific antibiotics

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Substances:

Year:  2017        PMID: 29151351      PMCID: PMC6034505          DOI: 10.1021/acsinfecdis.7b00172

Source DB:  PubMed          Journal:  ACS Infect Dis        ISSN: 2373-8227            Impact factor:   5.084


  58 in total

Review 1.  Progress and Works in Progress: Update on Flavivirus Vaccine Development.

Authors:  Matthew H Collins; Stefan W Metz
Journal:  Clin Ther       Date:  2017-07-25       Impact factor: 3.393

2.  Transition State Analogue Inhibitors of 5'-Deoxyadenosine/5'-Methylthioadenosine Nucleosidase from Mycobacterium tuberculosis.

Authors:  Hilda A Namanja-Magliano; Gary B Evans; Rajesh K Harijan; Peter C Tyler; Vern L Schramm
Journal:  Biochemistry       Date:  2017-09-07       Impact factor: 3.162

3.  Antiviral activity of the adenosine analogue BCX4430 against West Nile virus and tick-borne flaviviruses.

Authors:  Luděk Eyer; Darina Zouharová; Jana Širmarová; Martina Fojtíková; Michal Štefánik; Jan Haviernik; Radim Nencka; Erik de Clercq; Daniel Růžek
Journal:  Antiviral Res       Date:  2017-03-21       Impact factor: 5.970

Review 4.  Aotus monkeys: their great value for anti-malaria vaccines and drug testing.

Authors:  Sócrates Herrera; Blanca Liliana Perlaza; Anilza Bonelo; Myriam Arévalo-Herrera
Journal:  Int J Parasitol       Date:  2002-12-04       Impact factor: 3.981

5.  A complex of methylthioadenosine/S-adenosylhomocysteine nucleosidase, transition state analogue, and nucleophilic water identified by mass spectrometry.

Authors:  Shanzhi Wang; Jihyeon Lim; Keisha Thomas; Funing Yan; Ruth H Angeletti; Vern L Schramm
Journal:  J Am Chem Soc       Date:  2012-01-12       Impact factor: 15.419

6.  Hospital ward antibiotic prescribing and the risks of Clostridium difficile infection.

Authors:  Kevin Brown; Kim Valenta; David Fisman; Andrew Simor; Nick Daneman
Journal:  JAMA Intern Med       Date:  2015-04       Impact factor: 21.873

7.  Transition state analogue inhibitors of purine nucleoside phosphorylase from Plasmodium falciparum.

Authors:  Gregory A Kicska; Peter C Tyler; Gary B Evans; Richard H Furneaux; Kami Kim; Vern L Schramm
Journal:  J Biol Chem       Date:  2001-11-13       Impact factor: 5.157

8.  Targeting a novel Plasmodium falciparum purine recycling pathway with specific immucillins.

Authors:  Li-Min Ting; Wuxian Shi; Andrzej Lewandowicz; Vipender Singh; Agnes Mwakingwe; Matthew R Birck; Erika A Taylor Ringia; Graham Bench; Dennis C Madrid; Peter C Tyler; Gary B Evans; Richard H Furneaux; Vern L Schramm; Kami Kim
Journal:  J Biol Chem       Date:  2004-12-02       Impact factor: 5.157

9.  Plasmodium falciparum purine nucleoside phosphorylase: crystal structures, immucillin inhibitors, and dual catalytic function.

Authors:  Wuxian Shi; Li-Min Ting; Gregory A Kicska; Andrzej Lewandowicz; Peter C Tyler; Gary B Evans; Richard H Furneaux; Kami Kim; Steve C Almo; Vern L Schramm
Journal:  J Biol Chem       Date:  2004-02-23       Impact factor: 5.157

Review 10.  Pyrrolo[2,3-d]pyrimidine (7-deazapurine) as a privileged scaffold in design of antitumor and antiviral nucleosides.

Authors:  Pavla Perlíková; Michal Hocek
Journal:  Med Res Rev       Date:  2017-08-23       Impact factor: 12.944

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  12 in total

1.  Antibacterial Strategy against H. pylori: Inhibition of the Radical SAM Enzyme MqnE in Menaquinone Biosynthesis.

Authors:  Sumedh Joshi; Dmytro Fedoseyenko; Nilkamal Mahanta; Rodrigo G Ducati; Mu Feng; Vern L Schramm; Tadhg P Begley
Journal:  ACS Med Chem Lett       Date:  2019-02-15       Impact factor: 4.345

2.  Synthesis of modified 1,5-imino-d-xylitols as ligands for lysosomal β-glucocerebrosidase.

Authors:  Manuel Zoidl; Andreas Wolfsgruber; Michael Schalli; Seyed A Nasseri; Patrick Weber; Arnold E Stütz; Stephen G Withers; Tanja M Wrodnigg
Journal:  Monatsh Chem       Date:  2019-05-11       Impact factor: 1.451

Review 3.  Enzymatic Transition States and Drug Design.

Authors:  Vern L Schramm
Journal:  Chem Rev       Date:  2018-10-18       Impact factor: 60.622

4.  Characterization of 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidases from Borrelia burgdorferi: Antibiotic targets for Lyme disease.

Authors:  Kenneth A Cornell; Reece J Knippel; Gerald R Cortright; Meghan Fonken; Christian Guerrero; Amy R Hall; Kristen A Mitchell; John H Thurston; Patrick Erstad; Aoxiang Tao; Dong Xu; Nikhat Parveen
Journal:  Biochim Biophys Acta Gen Subj       Date:  2019-10-31       Impact factor: 3.770

5.  Identification of immucillin analogue natural compounds to inhibit Helicobacter pylori MTAN through high throughput virtual screening and molecular dynamics simulation.

Authors:  Divya S Raj; Chidhambara Priya Dharshini Kottaisamy; Waheetha Hopper; Umamaheswari Sankaran
Journal:  In Silico Pharmacol       Date:  2021-03-11

6.  N-Nonyloxypentyl-l-Deoxynojirimycin Inhibits Growth, Biofilm Formation and Virulence Factors Expression of Staphylococcus aureus.

Authors:  Eliana De Gregorio; Anna Esposito; Adriana Vollaro; Maria De Fenza; Daniele D'Alonzo; Antonella Migliaccio; Vita Dora Iula; Raffaele Zarrilli; Annalisa Guaragna
Journal:  Antibiotics (Basel)       Date:  2020-06-26

Review 7.  Interference With Quorum-Sensing Signal Biosynthesis as a Promising Therapeutic Strategy Against Multidrug-Resistant Pathogens.

Authors:  Osmel Fleitas Martínez; Pietra Orlandi Rigueiras; Állan da Silva Pires; William Farias Porto; Osmar Nascimento Silva; Cesar de la Fuente-Nunez; Octavio Luiz Franco
Journal:  Front Cell Infect Microbiol       Date:  2019-02-05       Impact factor: 5.293

Review 8.  Nucleoside Hydrolase NH 36: A Vital Enzyme for the Leishmania Genus in the Development of T-Cell Epitope Cross-Protective Vaccines.

Authors:  Clarisa Beatriz Palatnik-de-Sousa
Journal:  Front Immunol       Date:  2019-04-16       Impact factor: 7.561

9.  PMP-diketopiperazine adducts form at the active site of a PLP dependent enzyme involved in formycin biosynthesis.

Authors:  Sisi Gao; Huanting Liu; Valérie de Crécy-Lagard; Wen Zhu; Nigel G J Richards; James H Naismith
Journal:  Chem Commun (Camb)       Date:  2019-11-28       Impact factor: 6.222

10.  N-Alkylated Iminosugar Based Ligands: Synthesis and Inhibition of Human Lysosomal β-Glucocerebrosidase.

Authors:  Andreas Wolfsgruber; Martin Thonhofer; Patrick Weber; Seyed A Nasseri; Roland Fischer; Michael Schalli; Arnold E Stütz; Stephen G Withers; Tanja M Wrodnigg
Journal:  Molecules       Date:  2020-10-11       Impact factor: 4.411

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