Construction of photofunctional peptide conjugates through selective modification of N-terminal cysteine with cyclometallated iridium(iii) 2-formylphenylboronic acid complexes for organelle-specific imaging, enzyme activity sensing and photodynamic therapy
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
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Detail(s)
Original language | English |
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Pages (from-to) | 6186-6189 |
Journal / Publication | Chemical Communications (London) |
Volume | 60 |
Issue number | 48 |
Online published | 10 May 2024 |
Publication status | Published - 18 Jun 2024 |
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Abstract
Luminescent cyclometallated iridium(iii) complexes bearing a 2-formylphenylboronic acid moiety were designed; one of the complexes was utilised to modify peptides containing an N-terminal cysteine to afford luminescent conjugates with selective organelle-targeting or furin-responsive properties. © 2024 The Royal Society of Chemistry.
Citation Format(s)
Construction of photofunctional peptide conjugates through selective modification of N-terminal cysteine with cyclometallated iridium(iii) 2-formylphenylboronic acid complexes for organelle-specific imaging, enzyme activity sensing and photodynamic therapy. / Huang, Lili; Lee, Lawrence Cho-Cheung; Shum, Justin et al.
In: Chemical Communications (London), Vol. 60, No. 48, 18.06.2024, p. 6186-6189.
In: Chemical Communications (London), Vol. 60, No. 48, 18.06.2024, p. 6186-6189.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review