BacPROTACs targeting Clp protease: a promising strategy for anti-mycobacterial drug discovery

Autor(es)

Bonjorno, Andressa Francielli ; Pavan, Aline Renata ; Fernandes, Guilherme F. S. ; Scarim, Caue Benito ; Castagnolo, Daniele ; Dos Santos, Jean Leandro

• Tipo de documento: Artigo Científico
• Fonte: RONTIERS IN CHEMISTR; v. 12, p. 6-pg., 2024-01-31.

Resumo

Tuberculosis (TB) has claimed more lives over the course of two millennia than any other infectious disease worldwide. In 2021, the World Health Organization (WHO) estimated that 10.6 million people were diagnosed with TB, resulting in the deaths of 1.4 million HIV-negative individuals. The emergence of multidrug-resistant TB (MDR-TB), defined as resistance to at least rifampicin (RIF) and isoniazid (INH), and extensively drug-resistant TB (XDR-TB), poses the primary challenge to overcome in the coming years. We have recently conducted an extensive analysis of investments and research endeavours in the field, with the overarching objective of achieving the established milestone of TB eradication by the year 2030. Over the past several years, there has been notable progress in advancing a multitude of promising compounds, each possessing distinct mechanisms of action, into clinical phases of development. However, it is worth noting that strains of mycobacteria resistant to current antitubercular drugs have already emerged for some of these compounds The exploration of the innovative Proteolytic Target Chimeras (PROTACs) protein degradation approach has emerged as a viable avenue for the discovery of novel antimicrobials. While the ubiquitin system is exclusive to eukaryotic cells, certain bacteria use a similar degradation system that relies on the recognition of phosphorylated arginine residues (pArg) by the ClpC:ClpP (ClpCP) protease, thereby leading to protein degradation. In this opinion article, we have described and analized the advances in the use of PROTACs that leverage bacterial proteolytic machinery (BacPROTACs) to design new antitubercular agents. Scope Statement. The development of novel pharmaceuticals for tuberculosis treatment is deemed urgently necessary due to the emergence of resistant strains. In this context, the introduction of new technologies capable of alleviating the disease and attaining the objectives outlined by the World Health Organization is imperative. Among the innovative strategies, the degradation of proteins that are crucial for the survival of the bacillus holds promise for generating new medications, particularly those that are effective at treating latent (non-replicating) Mycobacterium tuberculosis. Within this perspective, we present the advancements and obstacles encountered in the exploration of new BacPROTAC compounds, with the intention of encouraging research and illuminating challenges associated with the implementation of BacPROTACs to address to the global tuberculosis crisis. (AU)

• Processo FAPESP: 20/13279-7 - Síntese e avaliação anti-Mycobacterium tuberculosis de novos derivados nitroimidazooxazina úteis para o tratamento da tuberculose multirresistente
• Beneficiário: Jean Leandro dos Santos
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 21/14973-7 - Síntese e avaliação de novos derivados nitroimidazooxazina planejados para atuar contra Mycobacterium tuberculosis resistente à fármacos
• Beneficiário: Andressa Francielli Bonjorno
• Modalidade de apoio: Bolsas no Brasil - Mestrado
• Processo FAPESP: 22/15844-9 - Síntese e avaliação of BacProtacs planejadas como agentes anti-Mycobacterium tuberculosis
• Beneficiário: Andressa Francielli Bonjorno
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Mestrado
• Processo FAPESP: 23/05739-6 - Estratégias para intervenção em complexos repressores do gene de gama-globina contendo Histona Deacetilase (HDAC-1 e HDAC-2)
• Beneficiário: Jean Leandro dos Santos
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 18/19523-7 - Planejamento, síntese e avaliação farmacológica de derivados de hidroxiuréia planejados como inibidores de histona deacetilase para Anemia Falciforme
• Beneficiário: Aline Renata Pavan
• Modalidade de apoio: Bolsas no Brasil - Doutorado