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Luminescent Peptide/Lanthanide(III) Complex Conjugates with Push-Pull Antennas: Application to One- and Two-Photon Microscopy Imaging.
Choi, Ji-Hyung; Fremy, Guillaume; Charnay, Thibault; Fayad, Nour; Pécaut, Jacques; Erbek, Sule; Hildebrandt, Niko; Martel-Frachet, Véronique; Grichine, Alexei; Sénèque, Olivier.
Afiliação
  • Choi JH; Université Grenoble Alpes, CNRS, CEA, IRIG, LCBM (UMR 5249), Grenoble F-38000, France.
  • Fremy G; Université Grenoble Alpes, CNRS, CEA, IRIG, LCBM (UMR 5249), Grenoble F-38000, France.
  • Charnay T; Université Grenoble Alpes, CNRS, DCM (UMR 5250), Grenoble F-38000, France.
  • Fayad N; Université Grenoble Alpes, CNRS, CEA, IRIG, LCBM (UMR 5249), Grenoble F-38000, France.
  • Pécaut J; Laboratoire COBRA (Chimie Organique, Bioorganique, Réactivite et Analyse), UMR 6014, CNRS, Université de Rouen Normandie, INSA, Mont-Saint-Aignan Cedex 76821, France.
  • Erbek S; Université Grenoble Alpes, CEA, CNRS, IRIG, SyMMES, Grenoble F-38000, France.
  • Hildebrandt N; Institute for Advanced Biosciences, Université Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Grenoble F-38000, France.
  • Martel-Frachet V; EPHE, PSL Research University, 4-14 Rue Ferrus, Paris 75014, France.
  • Grichine A; Laboratoire COBRA (Chimie Organique, Bioorganique, Réactivite et Analyse), UMR 6014, CNRS, Université de Rouen Normandie, INSA, Mont-Saint-Aignan Cedex 76821, France.
  • Sénèque O; Institute for Advanced Biosciences, Université Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Grenoble F-38000, France.
Inorg Chem ; 61(50): 20674-20689, 2022 Dec 19.
Article em En | MEDLINE | ID: mdl-36475655
Lanthanide(III) (Ln3+) complexes feature desirable luminescence properties for cell microscopy imaging, but cytosolic delivery of Ln3+ complexes and their use for 2P imaging of live cells are challenging. In this article, we describe the synthesis and spectroscopic characterizations of a series of Ln3+ complexes based on two ligands, L1 and L2, featuring extended picolinate push-pull antennas for longer wavelength absorption and 2P absorption properties as well as a free carboxylate function for conjugation to peptides. Several cell penetrating peptide/Ln3+ complex conjugates were then prepared with the most interesting luminescent complexes, Tb(L1) and Eu(L2), and with two cell penetrating peptides (CPPs), ZF5.3 and TP2. A spectroscopic analysis demonstrates that the luminescence properties of the complexes are not affected by conjugation to the peptide. The conjugates were evaluated for one-photon (1P) time-gated microscopy imaging, which suppresses biological background fluorescence, and 2P confocal microscopy. Whereas TP2-based conjugates were unable to enter cells, successful 1P and 2P imaging was performed with ZF5.3[Tb(L1)]. 2P confocal imaging suggests proper internalization and cytosolic delivery as expected for this CPP. Noteworthy, 2P confocal microscopy also allowed characterization of the luminescence properties of the complex (spectrum, lifetime) within the cell, opening the way to functional luminescent probes for 2P confocal imaging of live cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Elementos da Série dos Lantanídeos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Elementos da Série dos Lantanídeos Idioma: En Ano de publicação: 2022 Tipo de documento: Article