<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Wang H</submitter><funding>Taishan Scholar Project of Shandong Province</funding><funding>National Natural Science Foundation of China</funding><pubmed_abstract>&lt;b>Background:&lt;/b> The interaction between lysosomes and mitochondria includes not only mitophagy but also mitochondrion-lysosome contact (MLC) that enables the two organelles to exchange materials and information. In our study, we synthesised a biosensor with fluorescence characteristics that can image lysosomes for structured illumination microscopy and, in turn, examined morphological changes in mitochondria and the phenomenon of MLC under pathological conditions. &lt;b>Methods:&lt;/b> After designing and synthesising the biosensor, dubbed CNN, we performed an assay with a Cell Counting Kit-8 to detect CNN's toxicity in relation to H9C2 cardiomyocytes. We next analysed the co-localisation of CNN and the commercial lysosomal probe LTG in cells, qualitatively analysed the imaging characteristic</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>865173</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8965020</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lysosome-Targeted Biosensor for the Super-Resolution Imaging of Lysosome-Mitochondrion Interaction.</pubmed_title><pmcid>PMC8965020</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Shao X</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Fang G</pubmed_authors><pubmed_authors>Cui Y</pubmed_authors><pubmed_authors>Hu M</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Su Y</pubmed_authors><pubmed_authors>Dong B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lysosome-Targeted Biosensor for the Super-Resolution Imaging of Lysosome-Mitochondrion Interaction.</name><description>&lt;b>Background:&lt;/b> The interaction between lysosomes and mitochondria includes not only mitophagy but also mitochondrion-lysosome contact (MLC) that enables the two organelles to exchange materials and information. In our study, we synthesised a biosensor with fluorescence characteristics that can image lysosomes for structured illumination microscopy and, in turn, examined morphological changes in mitochondria and the phenomenon of MLC under pathological conditions. &lt;b>Methods:&lt;/b> After designing and synthesising the biosensor, dubbed CNN, we performed an assay with a Cell Counting Kit-8 to detect CNN's toxicity in relation to H9C2 cardiomyocytes. We next analysed the co-localisation of CNN and the commercial lysosomal probe LTG in cells, qualitatively analysed the imaging characteristic</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T07:35:11.528Z</modification><creation>2025-04-04T07:35:11.528Z</creation></dates><accession>S-EPMC8965020</accession><cross_references><pubmed>35370649</pubmed><doi>10.3389/fphar.2022.865173</doi></cross_references></HashMap>