Literature DB >> 21426021

New strategies in fighting TB: targeting Mycobacterium tuberculosis-secreted phosphatases MptpA & MptpB.

Ana P G Silva1, Lydia Tabernero.   

Abstract

Mycobacterium tuberculosis is the most successful human pathogen due to its ability to challenge the innate immune system and survive in the infected host for a lifetime. Although tuberculosis (TB) is a curable disease, severe multidrug resistance to traditional antibiotics has caused a resurgence of the infection worldwide. The secreted phosphatases MptpA and MptpB are key virulence factors that play important roles in survival of M. tuberculosis during macrophage infection. These enzymes are therefore attractive alternative targets for chemotherapy. In this review we analyze the structural features that characterize these two phosphatases and differentiate them from human homologs. Their structural peculiarities are important for drug-design considerations and the future development of selective inhibitors. We describe the recent efforts in developing specific, selective and cell-active inhibitors of MptpA and MptpB, and discuss their potential applications as alternative treatments of TB.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21426021     DOI: 10.4155/fmc.10.214

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  7 in total

1.  The apo-structure of the low molecular weight protein-tyrosine phosphatase A (MptpA) from Mycobacterium tuberculosis allows for better target-specific drug development.

Authors:  Tanja Stehle; Sridhar Sreeramulu; Frank Löhr; Christian Richter; Krishna Saxena; Hendrik R A Jonker; Harald Schwalbe
Journal:  J Biol Chem       Date:  2012-08-10       Impact factor: 5.157

2.  Mycobacterial Protein Tyrosine Phosphatases A and B Inhibitors Augment the Bactericidal Activity of the Standard Anti-tuberculosis Regimen.

Authors:  Noton K Dutta; Rongjun He; Michael L Pinn; Yantao He; Francis Burrows; Zhong-Yin Zhang; Petros C Karakousis
Journal:  ACS Infect Dis       Date:  2015-12-24       Impact factor: 5.084

3.  Highly Potent and Selective N-Aryl Oxamic Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B.

Authors:  Kasi Viswanatharaju Ruddraraju; Devesh Aggarwal; Congwei Niu; Erica Anne Baker; Ruo-Yu Zhang; Li Wu; Zhong-Yin Zhang
Journal:  J Med Chem       Date:  2020-08-21       Impact factor: 7.446

4.  Discovery of Mycobacterium tuberculosis protein tyrosine phosphatase B (PtpB) inhibitors from natural products.

Authors:  Alessandra Mascarello; Mattia Mori; Louise Domeneghini Chiaradia-Delatorre; Angela Camila Orbem Menegatti; Franco Delle Monache; Franco Ferrari; Rosendo Augusto Yunes; Ricardo José Nunes; Hernán Terenzi; Bruno Botta; Maurizio Botta
Journal:  PLoS One       Date:  2013-10-14       Impact factor: 3.240

5.  Alterporriol-type dimers from the mangrove endophytic fungus, Alternaria sp. (SK11), and their MptpB inhibitions.

Authors:  Guoping Xia; Jia Li; Hanxiang Li; Yuhua Long; Shao'e Lin; Yongjun Lu; Lei He; Yongcheng Lin; Lan Liu; Zhigang She
Journal:  Mar Drugs       Date:  2014-05-16       Impact factor: 5.118

6.  Asperlones A and B, dinaphthalenone derivatives from a mangrove endophytic fungus Aspergillus sp. 16-5C.

Authors:  Ze'en Xiao; Shao'e Lin; Chunbing Tan; Yongjun Lu; Lei He; Xishan Huang; Zhigang She
Journal:  Mar Drugs       Date:  2015-01-13       Impact factor: 5.118

7.  Structure-Based Design of MptpB Inhibitors That Reduce Multidrug-Resistant Mycobacterium tuberculosis Survival and Infection Burden in Vivo.

Authors:  Clare F Vickers; Ana P G Silva; Ajanta Chakraborty; Paulina Fernandez; Natalia Kurepina; Charis Saville; Yandi Naranjo; Miquel Pons; Laura S Schnettger; Maximiliano G Gutierrez; Steven Park; Barry N Kreiswith; David S Perlin; Eric J Thomas; Jennifer S Cavet; Lydia Tabernero
Journal:  J Med Chem       Date:  2018-09-10       Impact factor: 7.446

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.