Phenotypic consequences of the conoid detachment.

<p><b>(A)</b> U-ExM images of CPH1 (conoid marker) and APR1 (APR marker) without or without the conoid detached from the APR. Scale bar = 3 μm. <b>(B)</b> U-ExM of secretory organelles, with MIC2 used as a microneme marker and RON9 used as a rhoptry neck marker. Images...

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সংরক্ষণ করুন:
গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Romuald Haase (22339777) (author)
অন্যান্য লেখক: Bingjian Ren (22676577) (author), Albert Tell i Puig (22676580) (author), Alessandro Bonavoglia (19415718) (author), Jean-Baptiste Marq (375239) (author), Rémy Visentin (22676583) (author), Nicolas Dos Santos Pacheco (22676586) (author), Bohumil Maco (383443) (author), Ricardo Mondragón-Flores (10737057) (author), Oscar Vadas (2416228) (author), Dominique Soldati-Favre (79026) (author)
প্রকাশিত: 2025
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সংক্ষিপ্ত:<p><b>(A)</b> U-ExM images of CPH1 (conoid marker) and APR1 (APR marker) without or without the conoid detached from the APR. Scale bar = 3 μm. <b>(B)</b> U-ExM of secretory organelles, with MIC2 used as a microneme marker and RON9 used as a rhoptry neck marker. Images taken with the conoid attached or detached from the APR. Scale bar = 3 μm <b>(C)</b> Western blot analysis of ethanol-triggered microneme secretion. ESA, Excreted secreted antigens. <b>(D)</b>. Representative images of BIPPO triggered egress. Scale bar = 20 μm. <b>(E)</b> Left panel: representative images of STAT6-P-positive cells with a Tir1 strain. Right panel: Quantification of rhoptry secretion was performed to assess STAT-6 phosphorylation. At least 200 cell nuclei were counted for data plotting, <i>n</i> = 3. ATc = anhydrotetracycline. The data underlying this figure can be found in <a href="http://www.plosbiology.org/article/info:doi/10.1371/journal.pbio.3003506#pbio.3003506.s008" target="_blank">S2 Data</a>.</p>