Cascioferro Stella, Raffa Demetrio, Maggio Benedetta, Raimondi Maria Valeria, Schillaci Domenico, Daidone Giuseppe
Dipartimento di Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche, Sezione di Chimica e Tecnologie Farmaceutiche, Università degli Studi di Palermo , Via Archirafi 32, 90123 Palermo, Italy.
IEMEST, Istituto Euromediterraneo di Scienza e Tecnologia , Via Emerico Amari, 123, 90139 Palermo, Italy.
J Med Chem. 2015 Dec 10;58(23):9108-23. doi: 10.1021/acs.jmedchem.5b00779. Epub 2015 Aug 17.
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.
在此,我们描述了最有前景的小型合成有机化合物,它们是强效分选酶A抑制剂,具有开发成为抗毒力药物的潜力。分选酶A是一种由206个氨基酸组成的多肽,它催化两个连续反应:(i)硫酯形成和(ii)转肽反应。分选酶A通过将含LPXTG的蛋白质锚定到脂质II参与细菌黏附过程。分选酶A抑制剂不影响细菌生长,但它们能抑制致病菌株的毒力,从而预防由金黄色葡萄球菌或其他革兰氏阳性菌引起的感染。最有前景的抑制剂的疗效需要在体内感染模型中进行全面评估,以便选择适合治疗人类细菌感染的化合物。