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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/15385
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dc.contributor.authorChowdhury, Rajdeep-
dc.contributor.authorAddy, Partha Sarathi-
dc.date.accessioned2024-08-23T10:30:11Z-
dc.date.available2024-08-23T10:30:11Z-
dc.date.issued2023-10-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsabm.3c00704-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15385-
dc.description.abstractProtein misfolding and aggregation resulting in amyloid formation is directly linked to various diseases. Hence, there is keen interest in developing probes for the selective detection of such misfolded aggregated proteins. In this paper, we have shown the use of a nontoxic aggregation-induced emissive luminogen (AIEgen), BIDCPV, for the selective detection of insulin amyloid fibrils and their various stages of formation. We further verified the selective response of BIDCPV toward amyloid fibrils by testing the probe against Aβ 42 peptides, which is well known to form the fibrils. Additionally, the low toxicity, efficient cellular internalization capability, and photostability make BIDCPV a unique candidate for sensing protein aggregates inside mammalian cells.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectBiologyen_US
dc.subjectAggregation-Induced Emission (AIE)en_US
dc.subjectFluorescenceen_US
dc.subjectAmyloid fibrilsen_US
dc.subjectConfocal microscopyen_US
dc.titleNontoxic Aggregation-Induced Emissive Luminogen for the Detection of Amyloid Fibrils and Cellular Protein Aggregatesen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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