# Naturally occurring dinactin targets cpsA protein and kills Mycobacterium tuberculosis by disrupting the proton motive force

**Authors:** Gaoyan Wang, Wenqi Dong, Yajuan Bai, Yuxin Li, Hao Lu, Wenjia Lu, Chenchen Wang, Jia Tang, Pei Li, Rui Wang, Xiangru Wang, Huanchun Chen, Chen Tan

PMC · DOI: 10.1038/s42003-026-09654-3 · 2026-02-12

## TL;DR

Dinactin is a natural compound that kills tuberculosis bacteria by targeting a specific protein and disrupting cell energy.

## Contribution

Dinactin is a novel natural macrotetrolide that targets the cpsA protein and disrupts the proton motive force in Mycobacterium tuberculosis.

## Key findings

- Dinactin shows anti-tuberculosis activity against both replicating and non-replicating Mycobacterium tuberculosis.
- Genetic studies confirm that the cpsA gene is a potential target of dinactin.
- Dinactin enhances the effectiveness of existing drugs like rifampicin and isoniazid against drug-resistant strains.

## Abstract

Tuberculosis, especially drug-resistant tuberculosis remains a global threat, and new drugs are desperately needed to combat the spread of multidrug-resistant Mycobacterium tuberculosis. Here we describe a natural macrotetrolide dinactin with anti-tuberculosis activity against susceptive and non-replicating Mycobacterium tuberculosis. Dinactin can also synergistically enhance the anti-tuberculosis effect of rifampicin and isoniazid against drug-resistant strains.Furthermore, dinactin exhibited excellently antituberculosis effect in macrophage and Galleria mellonella models. Since the ionophore properties of dinactin, it not only enhanced cations transport and altered membrane permeability but also caused the dissipation of proton motive force and metabolic perturbations. Finally, through the selection of spontaneous resistant mutants and whole genome sequencing, non-synonymous single nucleotide polymorphisms were successfully identified in the cpsA gene of the LytR-Cps2A-Psr family. The dinactin-resistant mutants exhibited decreased in vitro drug sensitivity to dinactin without cross-resistance to first-line antituberculosis drugs. Genetic studies and molecular biology assays have subsequently confirmed cpsA as one of the potential targets for dinactin’s anti-tuberculosis activity. Collectively, these data indicate that dinactin could be a promising candidate for treating tuberculosis.

Dinactin disrupts the proton motive force of the cell membrane of Mycobacterium tuberculosis by targeting the LCP family protein and thereby kills the Mycobacterium tuberculosis in vitro and in vivo.

## Linked entities

- **Genes:** cpsA (carboxypeptidase CpsA) [NCBI Gene 1441846]
- **Proteins:** cpsA (carboxypeptidase CpsA)
- **Chemicals:** dinactin (PubChem CID 6916048), rifampicin (PubChem CID 135398735), isoniazid (PubChem CID 3767)
- **Diseases:** tuberculosis (MONDO:0018076), drug-resistant tuberculosis (MONDO:0041806)
- **Species:** Mycobacterium tuberculosis (taxon 1773), Galleria mellonella (taxon 7137)

## Full-text entities

- **Diseases:** Tuberculosis (MESH:D014376)
- **Chemicals:** rifampicin (MESH:D012293), Dinactin (MESH:C016520), macrotetrolide (-), isoniazid (MESH:D007538)
- **Species:** Mycobacterium tuberculosis subsp. tuberculosis (subspecies) [taxon 182785], Mycobacterium tuberculosis (species) [taxon 1773], Galleria mellonella (greater wax moth, species) [taxon 7137]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13009212/full.md

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Source: https://tomesphere.com/paper/PMC13009212