Structure of the central Staphylococcus aureus AAA+ protease MecA/ClpC/ClpP

Bacterial AAA+ proteases are composed of a AAA+ partner (e.g., ClpC) and an associated peptidase (e.g., ClpP). They represent ATP-fuelled and self-compartmentalized proteolytic machines that are crucial for stress resistance and virulence. ClpC requires cooperation with adaptor proteins such as MecA for activation and complex formation with ClpP. Here, we present the cryo-EM structure of the MecA/ClpC/ClpP complex from the major pathogen Staphylococcus aureus. MecA forms a dynamic crown on top of the ClpC/ClpP complex with its substrate-binding domain positioned near the ClpC pore site, likely facilitating substrate transfer. ClpC/ClpP complex formation involves ClpC P-loops and ClpP N-terminal β-hairpins, which insert into the central ClpC threading channel and contact sites next to the ClpC ATPase center. ClpC and ClpP interactions are asymmetric and dictated by the activity states of ClpC ATPase subunits. ClpP binding increases ClpC ATPase and threading activities in a β-hairpin dependent manner, illuminating an allosteric pathway in the cooperation of ATPase and peptidase components in bacterial AAA+ proteases.

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Publication Details

Journal
Communications Biology
Published
2025-10-14
DOI
https://doi.org/10.1038/s42003-025-08908-w
Citations
1
Primary Topic
Antimicrobial Resistance in Staphylococcus
Type
article
Field-Weighted Citation Impact
1.40

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article

Structure of the central Staphylococcus aureus AAA+ protease MecA/ClpC/ClpP

Stavros Azinas, K. Wallden, Axel Mogk, Panagiotis Katikaridis et al.
1 citations
Communications Biology
Antimicrobial Resistance in Staphylococcus
1.40
article

Structure of the central Staphylococcus aureus AAA+ protease MecA/ClpC/ClpP

Stavros Azinas, K. Wallden, Axel Mogk, Panagiotis Katikaridis, Adrien Schahl, Marta Carroni, Timo Jenne
article en
1 citations

Abstract

Bacterial AAA+ proteases are composed of a AAA+ partner (e.g., ClpC) and an associated peptidase (e.g., ClpP). They represent ATP-fuelled and self-compartmentalized proteolytic machines that are crucial for stress resistance and virulence. ClpC requires cooperation with adaptor proteins such as MecA for activation and complex formation with ClpP. Here, we present the cryo-EM structure of the MecA/ClpC/ClpP complex from the major pathogen Staphylococcus aureus. MecA forms a dynamic crown on top of the ClpC/ClpP complex with its substrate-binding domain positioned near the ClpC pore site, likely facilitating substrate transfer. ClpC/ClpP complex formation involves ClpC P-loops and ClpP N-terminal β-hairpins, which insert into the central ClpC threading channel and contact sites next to the ClpC ATPase center. ClpC and ClpP interactions are asymmetric and dictated by the activity states of ClpC ATPase subunits. ClpP binding increases ClpC ATPase and threading activities in a β-hairpin dependent manner, illuminating an allosteric pathway in the cooperation of ATPase and peptidase components in bacterial AAA+ proteases.

Communications BiologyVol. 8(1)
Stockholm University (SE), German Cancer Research Center (DE), Heidelberg University (DE), Science for Life Laboratory (SE), DKFZ-ZMBH Alliance (DE)
Deutsche Forschungsgemeinschaft, Knut och Alice Wallenbergs Stiftelse, Stockholms Universitet, Science for Life Laboratory, Stiftelsen för Strategisk Forskning
Openalex Percentile: Top 15%
Antimicrobial Resistance in Staphylococcus
1.40
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