Literature DB >> 26280844

Sortase A Inhibitors: Recent Advances and Future Perspectives.

Stella Cascioferro1,2, Demetrio Raffa1, Benedetta Maggio1, Maria Valeria Raimondi1, Domenico Schillaci1, Giuseppe Daidone1.   

Abstract

Here, we describe the most promising small synthetic organic compounds that act as potent Sortase A inhibitors and cater the potential to be developed as antivirulence drugs. Sortase A is a polypeptide of 206 amino acids, which catalyzes two sequential reactions: (i) thioesterification and (ii) transpeptidation. Sortase A is involved in the process of bacterial adhesion by anchoring LPXTG-containing proteins to lipid II. Sortase A inhibitors do not affect bacterial growth, but they restrain the virulence of pathogenic bacterial strains, thereby preventing infections caused by Staphylococcus aureus or other Gram-positive bacteria. The efficacy of the most promising inhibitors needs to be comprehensively evaluated in in vivo models of infection, in order to select compounds eligible for the treatment of bacterial infections in humans.

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Year:  2015        PMID: 26280844     DOI: 10.1021/acs.jmedchem.5b00779

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  31 in total

1.  Development of Potent and Selective S. aureus Sortase A Inhibitors Based on Peptide Macrocycles.

Authors:  Inmaculada Rentero Rebollo; Shawna McCallin; Davide Bertoldo; José Manuel Entenza; Philippe Moreillon; Christian Heinis
Journal:  ACS Med Chem Lett       Date:  2016-04-14       Impact factor: 4.345

2.  NMR structure-based optimization of Staphylococcus aureus sortase A pyridazinone inhibitors.

Authors:  Albert H Chan; Sung Wook Yi; Ethan M Weiner; Brendan R Amer; Christopher K Sue; Jeff Wereszczynski; Carly A Dillen; Silvia Senese; Jorge Z Torres; J Andrew McCammon; Lloyd S Miller; Michael E Jung; Robert T Clubb
Journal:  Chem Biol Drug Des       Date:  2017-03-06       Impact factor: 2.817

3.  Covalent sortase A inhibitor ML346 prevents Staphylococcus aureus infection of Galleria mellonella.

Authors:  Xiang-Na Guan; Tao Zhang; Teng Yang; Ze Dong; Song Yang; Lefu Lan; Jianhua Gan; Cai-Guang Yang
Journal:  RSC Med Chem       Date:  2021-11-01

4.  Lysine-Targeted Reversible Covalent Ligand Discovery for Proteins via Phage Display.

Authors:  Mengmeng Zheng; Fa-Jie Chen; Kaicheng Li; Rahi M Reja; Fredrik Haeffner; Jianmin Gao
Journal:  J Am Chem Soc       Date:  2022-08-17       Impact factor: 16.383

5.  A peptide from human β thymosin as a platform for the development of new anti-biofilm agents for Staphylococcus spp. and Pseudomonas aeruginosa.

Authors:  Domenico Schillaci; Angelo Spinello; Maria Grazia Cusimano; Stella Cascioferro; Giampaolo Barone; Maria Vitale; Vincenzo Arizza
Journal:  World J Microbiol Biotechnol       Date:  2016-06-23       Impact factor: 3.312

6.  Lysine-Targeting Reversible Covalent Inhibitors with Long Residence Time.

Authors:  Rahi M Reja; Wenjian Wang; Yuhan Lyu; Fredrik Haeffner; Jianmin Gao
Journal:  J Am Chem Soc       Date:  2022-01-18       Impact factor: 15.419

7.  A Novel Yeast Surface Display Method for Large-Scale Screen Inhibitors of Sortase A.

Authors:  Lin Wu; Huijun Li; Tianle Tang
Journal:  Bioengineering (Basel)       Date:  2017-01-24

8.  Streptococcus suis sortase A is Ca2+ independent and is inhibited by acteoside, isoquercitrin and baicalin.

Authors:  Fuguang Chen; Fang Xie; Baoling Yang; Chengcheng Wang; Siguo Liu; Yueling Zhang
Journal:  PLoS One       Date:  2017-03-20       Impact factor: 3.240

9.  Asymmetric Disulfanylbenzamides as Irreversible and Selective Inhibitors of Staphylococcus aureus Sortase A.

Authors:  Fabian Barthels; Gabriella Marincola; Tessa Marciniak; Matthias Konhäuser; Stefan Hammerschmidt; Jan Bierlmeier; Ute Distler; Peter R Wich; Stefan Tenzer; Dirk Schwarzer; Wilma Ziebuhr; Tanja Schirmeister
Journal:  ChemMedChem       Date:  2020-03-25       Impact factor: 3.466

10.  Bacterial Biofilm Inhibition in the Development of Effective Anti-Virulence Strategy.

Authors:  Barbara Parrino; Patrizia Diana; Girolamo Cirrincione; Stella Cascioferro
Journal:  Open Med Chem J       Date:  2018-08-31
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