Abstract
We have developed a fluorescent peptide conjugate (TrpNDIRGDfK) based on the coupling of cyclo(RGDfK) to a new tryptophan-tagged amino acid naphthalenediimide (TrpNDI). Confocal fluorescence microscopy coupled with fluorescence lifetime imaging (FLIM) mapping, single and two-photon fluorescence excitation, lifetime components and corresponding decay profiles were used as parameters able to investigate qualitatively the cellular behavior regarding the molecular environment and biolocalisation of TrpNDI and TrpNDI-RGDfK in cancer cells.
Original language | English |
---|---|
Pages (from-to) | 6901-6904 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 51 |
Issue number | 32 |
Early online date | 16 Jan 2015 |
DOIs | |
Publication status | Published - 25 Apr 2015 |
Fingerprint
Dive into the research topics of 'A fluorescent Arg–Gly–Asp (RGD) peptide–naphthalenediimide (NDI) conjugate for imaging integrin αvβ3in vitro'. Together they form a unique fingerprint.Profiles
-
Sofia Pascu, FRSC
- Department of Chemistry - Professor
- Centre for Sustainable Chemical Technologies (CSCT)
- Centre for Therapeutic Innovation
- Centre for Bioengineering & Biomedical Technologies (CBio)
- Institute of Sustainability and Climate Change
Person: Research & Teaching, Affiliate staff