Biology subjects

Hertle, A. P.

Publications and source records attributed to Hertle, A. P..

4 recordsLinked to original sources

bioRxiv2025

Insights into CPSFL1 Induced Membrane Dynamics: A Multifaceted Regulator Linking Vesicle Formation to Thylakoid Biogenesis

Light drives plant life through photosynthesis, a process that takes place in the thylakoid membrane of the chloroplast, an organelle of cyanobacterial origin. The formation of thylakoid membranes within the chloroplast involves the eukaryote-specific factor CHLOROPLAST SEC14 LIKE PROTEIN 1 (CPSFL1), which shares strong sequence homology with the vesicle trafficking regulator SEC14. CSPFL1 is essential for vesicle formation, yet its specific molecular function in this process has remained unclear. In this study, we characterized CSPFL1 functions both in vitro and in vivo. Using a minimal membrane system of giant unilamellar vesicles (GUVs), we show that CPSFL1 alone can induce vesiculation. This process is mediated by lipid binding and membrane deformation, driven by curvature sensing and lipid-protein electrostatics. When expressed in the prokaryote E. coli, the eukaryote-specific CSPFL1 induces membrane curvature and vesicle formation. Plastid CPSFL1 co-purifies with vesicular structures. Lipid compositional analysis of CPSFL1-induced vesicles from bacteria reveals the presence of quinone precursors as cargo, linking CSPFL-mediated vesicle formation to prenylquinone transport. Together, our data suggest that during plant evolution, the eukaryotic vesicle formation system was co-opted for the transport of membrane integral metabolites from the inner envelope to the thylakoid membrane.

plant biology↗

bioRxiv2024

SOQ1 functions as a methionine sulfoxide reductase in the chloroplast lumen for regulation of photoprotective qH in Arabidopsis

Photosynthetic organisms must balance light absorption and energy dissipation to prevent photo-oxidative damage. Non-photochemical quenching (NPQ) dissipates excess light energy as heat, with the quenching component qH providing sustained photoprotection. However, the molecular mechanism underlying qH induction remains unclear. Our study focuses on the thylakoid membrane protein SUPPRESSOR OF QUENCHING 1 (SOQ1) and its inhibition of qH through interaction with LIPOCALIN IN THE PLASTID (LCNP) in Arabidopsis thaliana. Structural homology of SOQ1 lumenal domains with bacterial disulfide bond protein D suggested potential thiol-disulfide exchange activity. In vitro assays determined that both SOQ1 thioredoxin-like (Trx-like) and C-terminal (CTD) domains contain a redox-active cysteine pair and evidenced electron transfer from Trx-like to CTD. Importantly, we found that SOQ1 lumenal domains exhibit methionine sulfoxide reductase (Msr) activity converting oxidized methionine residues in LCNP back to methionine, which thereby inactivates LCNP and prevents qH formation. Mutational analyses identified cysteine residues in SOQ1-CTD and methionine residues in LCNP as critical for qH suppression, supporting their role in redox regulation. Additionally, we found that the redox state of SOQ1 in vivo is light-dependent, shifting from reduced to oxidized under stress conditions, indicating a dynamic regulation of its activity. We conclude that the Trx-like domain of SOQ1 provides reducing power to its CTD displaying Msr activity. SOQ1 is therefore an unusual example of a protein possessing both a disulfide reductase and Msr domain in tandem. Our findings elucidate the redox-regulation mechanism of qH involving SOQ1-mediated methionine reduction of LCNP, providing insights into the intricate control of photoprotective processes in chloroplasts and enhancing our understanding of plant resilience under environmental stress.

plant biology↗

bioRxiv2024

New evidence for the presence and function of phosphoinositides (PPIs) in the chloroplast

Essential proteins such as the chloroplast-localized Sec14-like protein (CPSFL1) and the vesicle-inducing protein in plastids (VIPP1) have a high affinity for binding phosphoinositides (PPIs) in vitro. PPIs are a specific class of phospholipids characterized by a phosphorylated inositol head group, and while they make up a small fraction of total phospholipids, they are crucial for various regulatory functions. However, the precise subcellular localization of most PPI species in plants remains unclear due to their rapid turnover and low abundance Currently there is no documented evidence for the presence and function of phosphoinositides (PPIs) in chloroplasts. In our study, we developed genetically encoded biosensors targeted to plastids, allowing for the detection of several PPI isoforms, including PI3P, PI4P, PI5P, PI(4,5)P2, and PI(3,5)P2 within chloroplasts. We demonstrated the specificity of these biosensors through immunological methods and observed changes in their distribution patterns when co-expressed with PPI-modifying enzymes (cTP-SAC7, cTP-PTEN, and cTP-dOCRL). Our findings also revealed the association and potential interaction between PI3P and VIPP1. Importantly, we found that elevated PPI levels during stress conditions led to altered biosensor localization, and plants expressing PPI modifiers showed increased sensitivity to drought stress, highlighting the role of PPIs in plant stress responses.

plant biology↗

bioRxiv2022

The K+ exchange antiporter 3 senses the chloroplast energy status to synchronize photosynthesis

Plant photosynthesis contains two functional modules, the light-driven reactions in the thylakoid membrane and the carbon-fixing reactions in the chloroplast stroma. In nature, light availability for photosynthesis often undergoes massive and rapid fluctuations. Efficient and productive use of such variable light supply requires an instant crosstalk and rapid synchronization of both functional modules. Here, we show that this communication involves the stromal exposed regulatory C-terminus (RCT) of the thylakoid K+-exchange antiporter KEA3. RCT-mediated control of KEA3 contributes to the balance between light capture and photoprotection. By combining in silico, in vitro, and in vivo approaches, we demonstrate that the RCT senses the energy state of the chloroplast in form of both, phosphorylation and redox potential, in a pH-dependent manner and regulates KEA3 activity in response. Together our data pinpoint a regulatory feedback loop by which the stromal energy state orchestrates light capture and photoprotection via KEA3.

plant biology↗