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| Main Authors: | , , , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
mBio
2025
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| Online Access: | https://pubmed.ncbi.nlm.nih.gov/41247015/ |
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| _version_ | 1868266125112901632 |
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| author | Gong, Piqian Li, Guobang Li, Weixun Xu, Mengyuan Jiao, Xuyao Chen, Xudong Gao, Beile Gao, Xiang |
| author_facet | Gong, Piqian Li, Guobang Li, Weixun Xu, Mengyuan Jiao, Xuyao Chen, Xudong Gao, Beile Gao, Xiang Gong, Piqian Li, Guobang Li, Weixun Xu, Mengyuan Jiao, Xuyao Chen, Xudong Gao, Beile Gao, Xiang |
| collection | PubMed - marine biology |
| contents | Cryo-EM structure of the QseG-QseE complex reveals an accessory protein-driven two-component system activation mechanism. Gong, Piqian Li, Guobang Li, Weixun Xu, Mengyuan Jiao, Xuyao Chen, Xudong Gao, Beile Gao, Xiang Cryoelectron Microscopy Histidine Kinase Signal Transduction Protein Binding Bacterial Outer Membrane Proteins Bacterial Proteins Lipoproteins Escherichia coli Proteins Models, Molecular Protein Conformation Escherichia coli The two-component system (TCS) enables bacteria to sense and respond to environmental changes through histidine kinase-mediated signaling cascades. Although the core components of TCSs have been extensively studied, the molecular basis of accessory proteins in modulating histidine kinase activity remains poorly understood. Here, we report that the outer membrane lipoprotein QseG functions as an accessory protein that directly binds to and activates the histidine kinase QseE via its C-terminal domain. Cryo-electron microscopy (Cryo-EM) structural analysis of the QseG-QseE complex reveals a novel yet conserved interaction mode between an accessory lipoprotein and a histidine kinase, which bridges the outer membrane to cytoplasm. Furthermore, systematic truncation assays and photo-crosslinking experiments indicate that outer membrane-anchored QseG is sufficient and prone to engage with and activate the inner membrane histidine kinase QseE under cultured conditions. Our findings provide mechanistic details for accessory lipoprotein-mediated TCS activation, expanding our understanding of bacterial signaling. The evolutionary conservation of this interaction across bacterial pathogens underscores its broad biological significance and potential as a therapeutic target.IMPORTANCEThe classical TCS system in bacterial signal transduction is composed of two proteins-a histidine kinase and its cognate response regulator. More and more studies have revealed the presence of accessory proteins that can modulate the histidine kinase activity and affect signal transduction, but their mechanisms remain largely elusive. This study unveils a previously unrecognized mechanism by which bacterial accessory lipoproteins mediate TCS activation. We provide compelling evidence that QseG directly interacts with QseE through an evolutionarily conserved structural interface, readily and sufficiently activating QseE's autokinase activity and downstream signaling. Given the essential role of QseEF in bacterial virulence and stress adaptation, our findings pave the way for the development of antimicrobial strategies targeting this conserved lipoprotein-mediated activation mechanism. |
| format | Artículo científico |
| id | pubmed_41247015 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | mBio |
| record_format | pubmed |
| spellingShingle | Cryo-EM structure of the QseG-QseE complex reveals an accessory protein-driven two-component system activation mechanism. Gong, Piqian Li, Guobang Li, Weixun Xu, Mengyuan Jiao, Xuyao Chen, Xudong Gao, Beile Gao, Xiang Cryoelectron Microscopy Histidine Kinase Signal Transduction Protein Binding Bacterial Outer Membrane Proteins Bacterial Proteins Lipoproteins Escherichia coli Proteins Models, Molecular Protein Conformation Escherichia coli Cryo-EM structure of the QseG-QseE complex reveals an accessory protein-driven two-component system activation mechanism. Gong, Piqian Li, Guobang Li, Weixun Xu, Mengyuan Jiao, Xuyao Chen, Xudong Gao, Beile Gao, Xiang Cryoelectron Microscopy Histidine Kinase Signal Transduction Protein Binding Bacterial Outer Membrane Proteins Bacterial Proteins Lipoproteins Escherichia coli Proteins Models, Molecular Protein Conformation Escherichia coli The two-component system (TCS) enables bacteria to sense and respond to environmental changes through histidine kinase-mediated signaling cascades. Although the core components of TCSs have been extensively studied, the molecular basis of accessory proteins in modulating histidine kinase activity remains poorly understood. Here, we report that the outer membrane lipoprotein QseG functions as an accessory protein that directly binds to and activates the histidine kinase QseE via its C-terminal domain. Cryo-electron microscopy (Cryo-EM) structural analysis of the QseG-QseE complex reveals a novel yet conserved interaction mode between an accessory lipoprotein and a histidine kinase, which bridges the outer membrane to cytoplasm. Furthermore, systematic truncation assays and photo-crosslinking experiments indicate that outer membrane-anchored QseG is sufficient and prone to engage with and activate the inner membrane histidine kinase QseE under cultured conditions. Our findings provide mechanistic details for accessory lipoprotein-mediated TCS activation, expanding our understanding of bacterial signaling. The evolutionary conservation of this interaction across bacterial pathogens underscores its broad biological significance and potential as a therapeutic target.IMPORTANCEThe classical TCS system in bacterial signal transduction is composed of two proteins-a histidine kinase and its cognate response regulator. More and more studies have revealed the presence of accessory proteins that can modulate the histidine kinase activity and affect signal transduction, but their mechanisms remain largely elusive. This study unveils a previously unrecognized mechanism by which bacterial accessory lipoproteins mediate TCS activation. We provide compelling evidence that QseG directly interacts with QseE through an evolutionarily conserved structural interface, readily and sufficiently activating QseE's autokinase activity and downstream signaling. Given the essential role of QseEF in bacterial virulence and stress adaptation, our findings pave the way for the development of antimicrobial strategies targeting this conserved lipoprotein-mediated activation mechanism. |
| title | Cryo-EM structure of the QseG-QseE complex reveals an accessory protein-driven two-component system activation mechanism. |
| topic | Cryoelectron Microscopy Histidine Kinase Signal Transduction Protein Binding Bacterial Outer Membrane Proteins Bacterial Proteins Lipoproteins Escherichia coli Proteins Models, Molecular Protein Conformation Escherichia coli |
| url | https://pubmed.ncbi.nlm.nih.gov/41247015/ |