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Updated: May 30, 2026

Quantifiable and Inexpensive Cell-Free Fluorescent Method to Confirm the Ability of Novel Compounds to Chelate Iron
05:36

Quantifiable and Inexpensive Cell-Free Fluorescent Method to Confirm the Ability of Novel Compounds to Chelate Iron

Published on: February 23, 2024

A turn-on fluorescent iron complex and its cellular uptake.

Jy D Chartres1, Michael Busby, Mark J Riley

  • 1School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Queensland, Australia 4072.

Inorganic Chemistry
|August 5, 2011
PubMed
Summary

Researchers developed a fluorescent iron chelator to track iron within cells. This new ligand, L(1), helps visualize how iron moves in cells, aiding the study of iron overload disorders.

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Quantifiable and Inexpensive Cell-Free Fluorescent Method to Confirm the Ability of Novel Compounds to Chelate Iron
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Visualizing Single Molecular Complexes In Vivo Using Advanced Fluorescence Microscopy
11:26

Visualizing Single Molecular Complexes In Vivo Using Advanced Fluorescence Microscopy

Published on: September 8, 2009

Area of Science:

  • Biochemistry
  • Cell Biology
  • Medicinal Chemistry

Background:

  • Chronic iron overload disorders necessitate chelators that can enter cells, bind labile iron, and be excreted.
  • The intracellular labile iron pools and their mechanisms remain poorly understood.
  • Heterocyclic hydrazine-based chelators like benzoyl picolinoyl hydrazine (H(2)BPH) show promise in mobilizing intracellular iron.

Purpose of the Study:

  • To develop a fluorescent probe for visualizing intracellular iron complexation and transport.
  • To characterize a novel fluorescent chelator and its iron(III) complex.
  • To investigate the cellular uptake and localization of the iron-chelator complex.

Main Methods:

  • Synthesis and characterization of a novel fluorescent chelator (L(1)) by grafting rhodamine B onto H(2)BPH.
  • Spectroscopic and X-ray crystallographic analysis of the free ligand and its 1:2 iron(III) complex, [Fe(III)(L(1))(2)](3+).
  • Confocal fluorescence microscopy to observe cellular uptake and localization in HeLa cells.

Main Results:

  • A novel fluorescent chelator, L(1), was synthesized, which is nonfluorescent alone but strongly fluorescent upon complexation with Fe(III).
  • The structure of the free ligand and the 1:2 iron(III) complex, [Fe(III)(L(1))(2)](3+), were confirmed.
  • Confocal microscopy demonstrated rapid cellular entry of the [Fe(III)(L(1))(2)](3+) complex into HeLa cells, with localization in endosomes/lysosomes.

Conclusions:

  • The developed fluorescent chelator L(1) enables visualization of iron complexation and cellular trafficking.
  • The study provides insights into the cellular behavior of iron chelators, relevant for treating iron overload.
  • The findings support the potential of such fluorescent probes in studying intracellular iron dynamics.