Modern optical microscopy methods to study biomolecular condensates
DC Field | Value | Language |
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dc.contributor.author | Anisha Shakya | - |
dc.contributor.author | John T. King | - |
dc.date.accessioned | 2021-04-19T06:50:01Z | - |
dc.date.accessioned | 2021-04-19T06:50:01Z | - |
dc.date.available | 2021-04-19T06:50:01Z | - |
dc.date.available | 2021-04-19T06:50:01Z | - |
dc.date.created | 2021-03-24 | - |
dc.date.issued | 2021-04 | - |
dc.identifier.issn | 1359-0294 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/9506 | - |
dc.description.abstract | © 2021 Elsevier Ltd. Cells achieve highly intricate internal organization via membrane-bound and membraneless organelles. Research over the past decade has implicated liquid–liquid phase separation, a phenomenon by which charged and often disordered biological macromolecules assemble into reversible liquid-like condensates, as the mechanism of formation of membraneless organelles in cells. During the same period, optical microscopy saw exciting advancements, including the super-resolution revolution, that were quickly adopted by researchers in the biological community. Today, there exists a vast library of techniques capable of providing unprecedented information regarding the formation, function, and dynamics of biomolecular condensates. In this review, we discuss a select number of modern optical microscopy methods that are particularly suited for studying biomolecular condensates both in vitro and in cells, as well as the associated technical challenges. | - |
dc.language | 영어 | - |
dc.publisher | Elsevier Ltd | - |
dc.title | Modern optical microscopy methods to study biomolecular condensates | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000634561700011 | - |
dc.identifier.scopusid | 2-s2.0-85101326937 | - |
dc.identifier.rimsid | 75131 | - |
dc.contributor.affiliatedAuthor | Anisha Shakya | - |
dc.contributor.affiliatedAuthor | John T. King | - |
dc.identifier.doi | 10.1016/j.cocis.2021.101421 | - |
dc.identifier.bibliographicCitation | Current Opinion in Colloid and Interface Science, v.52 | - |
dc.relation.isPartOf | Current Opinion in Colloid and Interface Science | - |
dc.citation.title | Current Opinion in Colloid and Interface Science | - |
dc.citation.volume | 52 | - |
dc.type.docType | Review | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.subject.keywordPlus | FLUORESCENCE CORRELATION SPECTROSCOPY | - |
dc.subject.keywordPlus | STRUCTURED-ILLUMINATION MICROSCOPY | - |
dc.subject.keywordPlus | PARTICLE-TRACKING MICRORHEOLOGY | - |
dc.subject.keywordPlus | LIQUID PHASE-SEPARATION | - |
dc.subject.keywordPlus | CROSS-LINKING POLYMER | - |
dc.subject.keywordPlus | STIMULATED-EMISSION | - |
dc.subject.keywordPlus | 2-POINT MICRORHEOLOGY | - |
dc.subject.keywordPlus | RESOLUTION LIMIT | - |
dc.subject.keywordPlus | PROTEINS | - |
dc.subject.keywordPlus | VISCOELASTICITY | - |
dc.subject.keywordAuthor | Biomolecular condensates | - |
dc.subject.keywordAuthor | Fluorescence microscopy | - |
dc.subject.keywordAuthor | Membraneless organelles | - |
dc.subject.keywordAuthor | Super-resolution imaging | - |