Designing an intracellular fluorescent probe for glutathione: two modulation sites for selective signal transduction
dc.citation.epage | 3263 | en_US |
dc.citation.issueNumber | 12 | en_US |
dc.citation.spage | 3260 | en_US |
dc.citation.volumeNumber | 16 | en_US |
dc.contributor.author | Işık, M. | en_US |
dc.contributor.author | Guliyev, R. | en_US |
dc.contributor.author | Kolemen, S. | en_US |
dc.contributor.author | Altay, Y. | en_US |
dc.contributor.author | Senturk, B. | en_US |
dc.contributor.author | Tekinay, T. | en_US |
dc.contributor.author | Akkaya, E. U. | en_US |
dc.date.accessioned | 2016-02-08T10:50:57Z | |
dc.date.available | 2016-02-08T10:50:57Z | |
dc.date.issued | 2014 | en_US |
dc.department | Department of Chemistry | en_US |
dc.description.abstract | A selective probe for glutathione was designed and synthesized. The design incorporates spatial and photophysical constraints for the maximal emission signal. Thus, pHs, as well as the intracellular thiol concentrations, determine the emission signal intensity through a tight control of charge-transfer and PeT processes. The probe works satisfactorily inside the human breast adenocarcinoma cells, highlighting GSH distribution in the cytosol. | en_US |
dc.description.provenance | Made available in DSpace on 2016-02-08T10:50:57Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2014 | en |
dc.identifier.doi | 10.1021/ol501272z | en_US |
dc.identifier.eissn | 1523-7052 | |
dc.identifier.issn | 1523-7060 | |
dc.identifier.uri | http://hdl.handle.net/11693/25825 | |
dc.language.iso | English | en_US |
dc.publisher | American Chemical Society | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/ol501272z | en_US |
dc.source.title | Organic Letters | en_US |
dc.title | Designing an intracellular fluorescent probe for glutathione: two modulation sites for selective signal transduction | en_US |
dc.type | Article | en_US |
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