1. Academic Validation
  2. Tuning the Color Palette of Fluorescent Copper Sensors through Systematic Heteroatom Substitution at Rhodol Cores

Tuning the Color Palette of Fluorescent Copper Sensors through Systematic Heteroatom Substitution at Rhodol Cores

  • ACS Chem Biol. 2018 Jul 20;13(7):1844-1852. doi: 10.1021/acschembio.7b00748.
Shang Jia 1 Karla M Ramos-Torres 1 Safacan Kolemen 1 2 Cheri M Ackerman 1 Christopher J Chang 1 3 4
Affiliations

Affiliations

  • 1 Department of Chemistry , University of California , Berkeley , California 94720 , United States.
  • 2 Department of Chemistry , Koc University , Rumelifeneri Yolu, 34450 , Sariyer, Istanbul , Turkey.
  • 3 Department of Molecular and Cell Biology , University of California , Berkeley , California 94720 , United States.
  • 4 Howard Hughes Medical Institute , University of California , Berkeley , California 94720 , United States.
Abstract

Copper is an essential nutrient for sustaining life, and emerging data have expanded the roles of this metal in biology from its canonical functions as a static enzyme cofactor to dynamic functions as a transition metal signal. At the same time, loosely bound, labile copper pools can trigger oxidative stress and damaging events that are detrimental if misregulated. The signal/stress dichotomy of copper motivates the development of new chemical tools to study its spatial and temporal distributions in native biological contexts such as living cells. Here, we report a family of fluorescent copper sensors built upon carbon-, silicon-, and phosphorus-substituted rhodol dyes that enable systematic tuning of excitation/emission colors from orange to near-infrared. These probes can detect changes in labile copper levels in living cells upon copper supplementation and/or depletion. We demonstrate the ability of the carbon-rhodol based congener, Copper Carbo Fluor 1 (CCF1), to identify elevations in labile copper pools in the Atp7a-/- fibroblast cell model of the genetic copper disorder Menkes disease. Moreover, we showcase the utility of the red-emitting phosphorus-rhodol based dye Copper Phosphorus Fluor 1 (CPF1) in dual-color, dual-analyte imaging experiments with the green-emitting calcium indicator Calcium Green-1 to enable simultaneous detection of fluctuations in copper and calcium pools in living cells. The results provide a starting point for advancing tools to study the contributions of copper to health and disease and for exploiting the rapidly growing palette of heteroatom-substituted xanthene dyes to rationally tune the optical properties of fluorescent indicators for Other biologically important analytes.

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