Exchangeable Self‐Assembled Lanthanide Antennas for PLIM Microscopy

Author:

Ruiz‐Arias Alvaro1,Fueyo‐González Francisco23ORCID,Izquierdo‐García Carolina2,Navarro Amparo4ORCID,Gutiérrez‐Rodríguez Marta25,Herranz Rosario2ORCID,Burgio Chiara6,Reinoso Antonio6,Cuerva Juan M.7ORCID,Orte Angel1ORCID,González‐Vera Juan A.12ORCID

Affiliation:

1. Nanoscopy-UGR Laboratory. Departamento de Fisicoquímica Unidad de Excelencia de Química Aplicada a Biomedicina y Medioambiente Facultad de Farmacia Universidad de Granada Campus Cartuja 18071 Granada Spain

2. Instituto de Química Médica (IQM-CSIC) Juan de la Cierva 3 28006 Madrid Spain

3. Current address: Department of Medicine Translational Transplant Research Center Immunology Institute Icahn School of Medicine at Mount Sinai New York USA

4. Departamento de Química Física y Analítica Facultad de Ciencias Experimentales Universidad de Jaén 23071 Jaén Spain

5. PTI-Global Health CSIC Juan de la Cierva 3 28006 Madrid Spain

6. Departamento de Bioquímica y Biología Molecular II Facultad de Farmacia Universidad de Granada Campus Cartuja 18071 Granada Spain

7. Departamento de Química Orgánica Unidad de Excelencia de Química Aplicada a Biomedicina y Medioambiente Facultad de Ciencias Universidad de Granada Campus Fuentenueva 18071 Granada Spain

Abstract

AbstractLanthanides have unique photoluminescence (PL) emission properties, including very long PL lifetimes. This makes them ideal for biological imaging applications, especially using PL lifetime imaging microscopy (PLIM). PLIM is an inherently multidimensional technique with exceptional advantages for quantitative biological imaging. Unfortunately, due to the required prolonged acquisitions times, photobleaching of lanthanide PL emission currently constitutes one of the main drawbacks of PLIM. In this study, we report a small aqueous‐soluble, lanthanide antenna, 8‐methoxy‐2‐oxo‐1,2,4,5‐tetrahydrocyclopenta[de]quinoline‐3‐phosphonic acid, PAnt, specifically designed to dynamically interact with lanthanide ions, serving as exchangeable dye aimed at mitigating photobleaching in PLIM microscopy in cellulo. Thus, self‐assembled lanthanide complexes that may be photobleached during image acquisition are continuously replenished by intact lanthanide antennas from a large reservoir. Remarkably, our self‐assembled lanthanide complex clearly demonstrated a significant reduction of PL photobleaching when compared to well‐established lanthanide cryptates, used for bioimaging. This concept of exchangeable lanthanide antennas opens new possibilities for quantitative PLIM bioimaging.

Funder

Agencia Estatal de Investigación

Consejería de Transformación Económica, Industria, Conocimiento y Universidades

Consejo Superior de Investigaciones Científicas

Publisher

Wiley

Subject

General Medicine

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