Observing Extremely Weak Protein-Protein Interactions with Conventional Single-Molecule Fluorescence Microscopy
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Janghyun Yoo | - |
dc.contributor.author | Tae-Sun Lee | - |
dc.contributor.author | Byungsan Choi | - |
dc.contributor.author | Min Ju Shon | - |
dc.contributor.author | Tae-Young Yoon | - |
dc.date.available | 2017-01-20T08:30:46Z | - |
dc.date.created | 2016-11-23 | - |
dc.date.issued | 2016-11 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/3240 | - |
dc.description.abstract | Extremely weak protein-protein interactions (PPIs), signified by micromolar or even millimolar dissociation constants, are one of the keys to understanding the rapid responses of cellular systems. Although single-molecule methods are particularly useful in determining kinetics of biological processes, their application is largely limited to rather strong interactions because of the diffraction-limited observation volume. In this study, we report a single-molecule method that allows the characterization of PPIs using a prey concentration 4 orders of magnitude lower than the dissociation constant. Instead of increasing the concentration of diffusing molecules, which is inevitably limited by the optical diffraction limit, we employed an increased density of surface bait protein. The low occupancy of the surface baits permitted determination of the kinetics with single-molecule resolution. We used this approach to study a PPI network consisting of Ras and its downstream proteins including full-length Rafs and catalytic subunits of phosphoinositide 3-kinase. © 2016 American Chemical Society | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Observing Extremely Weak Protein-Protein Interactions with Conventional Single-Molecule Fluorescence Microscopy | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000387095000019 | - |
dc.identifier.scopusid | 2-s2.0-84994335456 | - |
dc.identifier.rimsid | 57715 | - |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Janghyun Yoo | - |
dc.contributor.affiliatedAuthor | Tae-Sun Lee | - |
dc.contributor.affiliatedAuthor | Byungsan Choi | - |
dc.contributor.affiliatedAuthor | Min Ju Shon | - |
dc.contributor.affiliatedAuthor | Tae-Young Yoon | - |
dc.identifier.doi | 10.1021/jacs.6b09542 | - |
dc.identifier.bibliographicCitation | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.138, no.43, pp.14238 - 14241 | - |
dc.citation.title | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.citation.volume | 138 | - |
dc.citation.number | 43 | - |
dc.citation.startPage | 14238 | - |
dc.citation.endPage | 14241 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 5 | - |
dc.description.scptc | 4 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | SCANNING OPTICAL MICROSCOPY | - |
dc.subject.keywordPlus | RAS | - |
dc.subject.keywordPlus | BIOLOGY | - |
dc.subject.keywordPlus | BINDING | - |
dc.subject.keywordPlus | LIMIT | - |