PubMed:28604678 JSONTXT

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    LitCoin-entities-OrganismTaxon-PD

    {"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T1","span":{"begin":441,"end":446},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"NCBItxid:9606"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-sentences

    {"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":121},"obj":"Sentence"},{"id":"T2","span":{"begin":122,"end":270},"obj":"Sentence"},{"id":"T3","span":{"begin":271,"end":384},"obj":"Sentence"},{"id":"T4","span":{"begin":385,"end":546},"obj":"Sentence"},{"id":"T5","span":{"begin":547,"end":733},"obj":"Sentence"},{"id":"T6","span":{"begin":734,"end":932},"obj":"Sentence"},{"id":"T7","span":{"begin":933,"end":1074},"obj":"Sentence"},{"id":"T8","span":{"begin":1075,"end":1249},"obj":"Sentence"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-entities

    {"project":"LitCoin-entities","denotations":[{"id":"13081","span":{"begin":28,"end":37},"obj":"GeneOrGeneProduct"},{"id":"13082","span":{"begin":65,"end":69},"obj":"GeneOrGeneProduct"},{"id":"13083","span":{"begin":126,"end":186},"obj":"GeneOrGeneProduct"},{"id":"13084","span":{"begin":271,"end":280},"obj":"GeneOrGeneProduct"},{"id":"13085","span":{"begin":413,"end":422},"obj":"GeneOrGeneProduct"},{"id":"13086","span":{"begin":441,"end":446},"obj":"OrganismTaxon"},{"id":"13087","span":{"begin":547,"end":556},"obj":"GeneOrGeneProduct"},{"id":"13088","span":{"begin":582,"end":588},"obj":"GeneOrGeneProduct"},{"id":"13089","span":{"begin":589,"end":593},"obj":"GeneOrGeneProduct"},{"id":"13090","span":{"begin":648,"end":657},"obj":"GeneOrGeneProduct"},{"id":"13091","span":{"begin":712,"end":721},"obj":"GeneOrGeneProduct"},{"id":"13092","span":{"begin":748,"end":752},"obj":"GeneOrGeneProduct"},{"id":"13093","span":{"begin":753,"end":758},"obj":"GeneOrGeneProduct"},{"id":"13094","span":{"begin":771,"end":780},"obj":"GeneOrGeneProduct"},{"id":"13095","span":{"begin":816,"end":820},"obj":"GeneOrGeneProduct"},{"id":"13096","span":{"begin":919,"end":923},"obj":"GeneOrGeneProduct"},{"id":"13097","span":{"begin":928,"end":931},"obj":"ChemicalEntity"},{"id":"13098","span":{"begin":1032,"end":1041},"obj":"GeneOrGeneProduct"},{"id":"13099","span":{"begin":1069,"end":1073},"obj":"GeneOrGeneProduct"},{"id":"13100","span":{"begin":1086,"end":1095},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A1","pred":"db_id","subj":"13081","obj":"NCBIGene:128866"},{"id":"A2","pred":"db_id","subj":"13081","obj":"NCBIGene:27243"},{"id":"A3","pred":"db_id","subj":"13081","obj":"NCBIGene:51652"},{"id":"A4","pred":"db_id","subj":"13082","obj":"NCBIGene:27183"},{"id":"A5","pred":"db_id","subj":"13082","obj":"NCBIGene:9525"},{"id":"A6","pred":"db_id","subj":"13083","obj":"NCBIGene:128866"},{"id":"A7","pred":"db_id","subj":"13083","obj":"NCBIGene:27243"},{"id":"A8","pred":"db_id","subj":"13083","obj":"NCBIGene:51652"},{"id":"A9","pred":"db_id","subj":"13084","obj":"NCBIGene:128866"},{"id":"A10","pred":"db_id","subj":"13084","obj":"NCBIGene:27243"},{"id":"A11","pred":"db_id","subj":"13084","obj":"NCBIGene:51652"},{"id":"A12","pred":"db_id","subj":"13085","obj":"NCBIGene:128866"},{"id":"A13","pred":"db_id","subj":"13085","obj":"NCBIGene:27243"},{"id":"A14","pred":"db_id","subj":"13085","obj":"NCBIGene:51652"},{"id":"A15","pred":"db_id","subj":"13086","obj":"NCBITaxon:9606"},{"id":"A16","pred":"db_id","subj":"13087","obj":"NCBIGene:128866"},{"id":"A17","pred":"db_id","subj":"13087","obj":"NCBIGene:27243"},{"id":"A18","pred":"db_id","subj":"13087","obj":"NCBIGene:51652"},{"id":"A19","pred":"db_id","subj":"13088","obj":"NCBIGene:27183"},{"id":"A20","pred":"db_id","subj":"13088","obj":"NCBIGene:9525"},{"id":"A21","pred":"db_id","subj":"13089","obj":"NCBIGene:27183"},{"id":"A22","pred":"db_id","subj":"13089","obj":"NCBIGene:9525"},{"id":"A23","pred":"db_id","subj":"13090","obj":"NCBIGene:128866"},{"id":"A24","pred":"db_id","subj":"13090","obj":"NCBIGene:27243"},{"id":"A25","pred":"db_id","subj":"13090","obj":"NCBIGene:51652"},{"id":"A26","pred":"db_id","subj":"13091","obj":"NCBIGene:128866"},{"id":"A27","pred":"db_id","subj":"13091","obj":"NCBIGene:27243"},{"id":"A28","pred":"db_id","subj":"13091","obj":"NCBIGene:51652"},{"id":"A29","pred":"db_id","subj":"13092","obj":"NCBIGene:27243"},{"id":"A30","pred":"db_id","subj":"13093","obj":"NCBIGene:51652"},{"id":"A31","pred":"db_id","subj":"13094","obj":"NCBIGene:128866"},{"id":"A32","pred":"db_id","subj":"13094","obj":"NCBIGene:27243"},{"id":"A33","pred":"db_id","subj":"13094","obj":"NCBIGene:51652"},{"id":"A34","pred":"db_id","subj":"13095","obj":"NCBIGene:128866"},{"id":"A35","pred":"db_id","subj":"13095","obj":"NCBIGene:29082"},{"id":"A36","pred":"db_id","subj":"13096","obj":"NCBIGene:27183"},{"id":"A37","pred":"db_id","subj":"13096","obj":"NCBIGene:9525"},{"id":"A38","pred":"db_id","subj":"13097","obj":"MESH:D000255"},{"id":"A39","pred":"db_id","subj":"13098","obj":"NCBIGene:128866"},{"id":"A40","pred":"db_id","subj":"13098","obj":"NCBIGene:27243"},{"id":"A41","pred":"db_id","subj":"13098","obj":"NCBIGene:51652"},{"id":"A42","pred":"db_id","subj":"13099","obj":"NCBIGene:27183"},{"id":"A43","pred":"db_id","subj":"13099","obj":"NCBIGene:9525"},{"id":"A44","pred":"db_id","subj":"13100","obj":"NCBIGene:128866"},{"id":"A45","pred":"db_id","subj":"13100","obj":"NCBIGene:27243"},{"id":"A46","pred":"db_id","subj":"13100","obj":"NCBIGene:51652"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-GeneOrGeneProduct-v0

    {"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":28,"end":37},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":38,"end":48},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":52,"end":61},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":65,"end":69},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":73,"end":80},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":109,"end":120},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":136,"end":143},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":165,"end":174},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":176,"end":181},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":183,"end":186},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":187,"end":195},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":237,"end":246},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":258,"end":269},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":271,"end":280},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":300,"end":310},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":331,"end":335},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":413,"end":422},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":447,"end":452},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":486,"end":497},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":535,"end":545},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":547,"end":556},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":582,"end":588},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":589,"end":593},"obj":"GeneOrGeneProduct"},{"id":"T24","span":{"begin":648,"end":657},"obj":"GeneOrGeneProduct"},{"id":"T25","span":{"begin":689,"end":697},"obj":"GeneOrGeneProduct"},{"id":"T26","span":{"begin":712,"end":721},"obj":"GeneOrGeneProduct"},{"id":"T27","span":{"begin":748,"end":752},"obj":"GeneOrGeneProduct"},{"id":"T28","span":{"begin":753,"end":758},"obj":"GeneOrGeneProduct"},{"id":"T29","span":{"begin":771,"end":780},"obj":"GeneOrGeneProduct"},{"id":"T30","span":{"begin":788,"end":792},"obj":"GeneOrGeneProduct"},{"id":"T31","span":{"begin":796,"end":800},"obj":"GeneOrGeneProduct"},{"id":"T32","span":{"begin":816,"end":820},"obj":"GeneOrGeneProduct"},{"id":"T33","span":{"begin":867,"end":873},"obj":"GeneOrGeneProduct"},{"id":"T34","span":{"begin":919,"end":923},"obj":"GeneOrGeneProduct"},{"id":"T35","span":{"begin":928,"end":931},"obj":"GeneOrGeneProduct"},{"id":"T36","span":{"begin":933,"end":937},"obj":"GeneOrGeneProduct"},{"id":"T37","span":{"begin":951,"end":956},"obj":"GeneOrGeneProduct"},{"id":"T38","span":{"begin":985,"end":991},"obj":"GeneOrGeneProduct"},{"id":"T39","span":{"begin":1010,"end":1017},"obj":"GeneOrGeneProduct"},{"id":"T40","span":{"begin":1032,"end":1041},"obj":"GeneOrGeneProduct"},{"id":"T41","span":{"begin":1069,"end":1073},"obj":"GeneOrGeneProduct"},{"id":"T42","span":{"begin":1086,"end":1095},"obj":"GeneOrGeneProduct"},{"id":"T43","span":{"begin":1199,"end":1204},"obj":"GeneOrGeneProduct"},{"id":"T44","span":{"begin":1239,"end":1248},"obj":"GeneOrGeneProduct"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-GeneOrGeneProduct-v2

    {"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":28,"end":37},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":65,"end":69},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":109,"end":120},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":176,"end":181},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":258,"end":269},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":271,"end":280},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":413,"end":422},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":486,"end":497},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":547,"end":556},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":582,"end":588},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":589,"end":593},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":648,"end":657},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":689,"end":697},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":712,"end":721},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":748,"end":752},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":753,"end":758},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":771,"end":780},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":788,"end":792},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":796,"end":800},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":816,"end":820},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":867,"end":873},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":919,"end":923},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":1032,"end":1041},"obj":"GeneOrGeneProduct"},{"id":"T24","span":{"begin":1069,"end":1073},"obj":"GeneOrGeneProduct"},{"id":"T25","span":{"begin":1086,"end":1095},"obj":"GeneOrGeneProduct"},{"id":"T26","span":{"begin":1199,"end":1204},"obj":"GeneOrGeneProduct"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-GeneOrGeneProduct-v3

    {"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":28,"end":37},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":65,"end":69},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":176,"end":181},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":271,"end":280},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":413,"end":422},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":486,"end":497},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":547,"end":556},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":582,"end":588},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":589,"end":593},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":648,"end":657},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":712,"end":721},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":748,"end":752},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":753,"end":758},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":771,"end":780},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":816,"end":820},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":919,"end":923},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":1032,"end":1041},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":1069,"end":1073},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":1086,"end":1095},"obj":"GeneOrGeneProduct"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-NCBITaxon-2

    {"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":441,"end":446},"obj":"OrganismTaxon"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-Chemical-MeSH-CHEBI

    {"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T1","span":{"begin":582,"end":588},"obj":"ChemicalEntity"},{"id":"T2","span":{"begin":928,"end":931},"obj":"ChemicalEntity"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D000251"},{"id":"A2","pred":"ID:","subj":"T2","obj":"http://purl.obolibrary.org/obo/CHEBI_30616"},{"id":"A3","pred":"ID:","subj":"T2","obj":"http://purl.obolibrary.org/obo/CHEBI_15422"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}

    LitCoin-training-merged

    {"project":"LitCoin-training-merged","denotations":[{"id":"T2","span":{"begin":928,"end":931},"obj":"ChemicalEntity"},{"id":"T1","span":{"begin":582,"end":588},"obj":"ChemicalEntity"},{"id":"T19","span":{"begin":1086,"end":1095},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":1069,"end":1073},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":1032,"end":1041},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":919,"end":923},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":816,"end":820},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":771,"end":780},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":753,"end":758},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":748,"end":752},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":712,"end":721},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":648,"end":657},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":589,"end":593},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":582,"end":588},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":547,"end":556},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":486,"end":497},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":413,"end":422},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":271,"end":280},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":176,"end":181},"obj":"GeneOrGeneProduct"},{"id":"T11476","span":{"begin":65,"end":69},"obj":"GeneOrGeneProduct"},{"id":"T49188","span":{"begin":28,"end":37},"obj":"GeneOrGeneProduct"},{"id":"T78992","span":{"begin":441,"end":446},"obj":"OrganismTaxon"}],"attributes":[{"id":"A3","pred":"ID:","subj":"T2","obj":"http://purl.obolibrary.org/obo/CHEBI_15422"},{"id":"A2","pred":"ID:","subj":"T2","obj":"http://purl.obolibrary.org/obo/CHEBI_30616"},{"id":"A1","pred":"ID:","subj":"T1","obj":"D000251"}],"text":"Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis.\nThe endosomal sorting complex required for transport (ESCRT)-III mediates membrane fission in fundamental cellular processes, including cytokinesis. ESCRT-III is thought to form persistent filaments that over time increase their curvature to constrict membranes. Unexpectedly, we found that ESCRT-III at the midbody of human cells rapidly turns over subunits with cytoplasmic pools while gradually forming larger assemblies. ESCRT-III turnover depended on the ATPase VPS4, which accumulated at the midbody simultaneously with ESCRT-III subunits, and was required for assembly of functional ESCRT-III structures. In vitro, the Vps2/Vps24 subunits of ESCRT-III formed side-by-side filaments with Snf7 and inhibited further polymerization, but the growth inhibition was alleviated by the addition of Vps4 and ATP. High-speed atomic force microscopy further revealed highly dynamic arrays of growing and shrinking ESCRT-III spirals in the presence of Vps4. Continuous ESCRT-III remodelling by subunit turnover might facilitate shape adaptions to variable membrane geometries, with broad implications for diverse cellular processes."}