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A major challenge towards the realization of an autonomous synthetic cell resides in the encoding of a division machinery in a genetic programme. In the bacterial cell cycle, the assembly of cytoskeletal proteins into a ring defines the division site. At the onset of the formation of the Escherichia coli divisome, a proto-ring consisting of FtsZ and its membrane-recruiting proteins takes place. Here, we show that FtsA-FtsZ ring-like structures driven by cell-free gene expression can be reconstituted on planar membranes and inside liposome compartments. Such cytoskeletal structures are found to constrict the liposome, generating elongated membrane necks and budding vesicles. Additional expression of the FtsZ cross-linker protein ZapA yields more rigid FtsZ bundles that attach to the membrane but fail to produce budding spots or necks in liposomes. These results demonstrate that gene-directed protein synthesis and assembly of membrane-constricting FtsZ-rings can be combined in a liposome-based artificial cell.
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http://dx.doi.org/10.1038/s42003-020-01258-9 | DOI Listing |
bioRxiv
August 2025
Department of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706.
Opsins are highly abundant retinal proteins in the membranes of photoheterotrophic bacteria. However, some microbial genomes encode an but lack the gene for the final enzyme in retinal synthesis. To account for this paradox, we hypothesized that bacterial opsins play a role in membrane structure and/or biogenesis independent from their potential for light-driven signaling or proton pumping.
View Article and Find Full Text PDFRegen Med
July 2025
Department of Stomatology, Lianyungang Clinical College of Nanjing Medical University, The First Affiliated Hospital of Kangda College of Nanjing Medical University, The Affiliated Lianyungang Hospital of Xuzhou Medical UniversityThe First People's Hospital of Lianyungang city, Lianyungang, Jiangsu,
Bone regeneration represents a key objective in bone tissue engineering and involves a series of coordinated biological processes, including immunomodulation, neuroregulation, angiogenesis, and osteogenesis. Recent studies have underscored the therapeutic potential of extracellular vesicles (EVs) in promoting osteogenesis and facilitating the repair of bone defects, supporting their application as a promising cell-free strategy in regenerative medicine. Migrasomes, vesicle-like organelles anchored to retraction fibers and first identified in 2015, have emerged as key mediators in intercellular communication, lateral transfer of mRNA and proteins, and mitochondrial homeostasis.
View Article and Find Full Text PDFJ Extracell Biol
July 2025
Chemical & Biomedical Engineering, FAMU-FSU College of Engineering Florida State University Tallahassee Florida USA.
Human mesenchymal stem cells (hMSCs) have been under investigation in preclinical and clinical settings for treating neurological disorders in recent years. Predominantly due to paracrine effects , hMSC-secreted extracellular vesicles (EVs) are at the forefront of these investigations. In this study, the therapeutic efficacy of hypoxia hMSCs and the secreted EVs labelled with iron oxides was evaluated in a preclinical model of ischemic stroke.
View Article and Find Full Text PDFPLoS One
July 2025
MOE Engineering Research Center of Gene Technology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Cell-free DNA (cfDNA) is increasingly studied for its diverse applications in non-invasive detection. Non-randomly cleaved by nucleases and released into the bloodstream, cfDNA exhibits a variety of intrinsic fragmentation patterns indicative of cell status. Particularly, these fragmentation patterns have recently been demonstrated to be effective in predicting cancer and its tissue-of-origin, owing to increased variation of fragmentation features observed in tumor patients.
View Article and Find Full Text PDFGene
September 2025
Department for BioMedical Research, Urology Research Laboratory, University of Bern, Bern, Switzerland; Translational Organoid Models, Department for BioMedical Research, University of Bern, Bern, Switzerland; Department of Urology, Inselspital, Bern University Hospital, Bern, Switzerland.
In this edition of Gene's 'Editor's Corner,' we highlight the emerging potential of extracellular vesicle-derived miRNAs as valuable biomarkers for prostate cancer diagnostics. In the recent issue of Gene (Gene 939, 2025, 149186), Nobrega et al. 1 present a compelling study that advances the field of liquid biopsy by comparing extracellular vesicle-incorporated microRNAs (EV-miRNAs) with cell-free microRNAs (cfmiRNAs) as biomarkers for prostate cancer.
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