TY - JOUR
T1 - Enhanced Binding of Zn2+ Using a Sulfur Version of o-Aminophenol-Triacetate (APTRA): Introducing S-APTRA and Derivatives
AU - Hogg, Christopher
AU - Duncan, Laura L.
AU - Parker, David
AU - Gareth Williams, J. A.
N1 - We thank Durham University for the award of Durham Doctoral Studentships to C.H. and L.L.D.
Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/5/19
Y1 - 2025/5/19
N2 - Ortho-aminophenol-N,N,O-triacetate (APTRA) is a pentadentate ligand adopted for the selective binding of Mg2+. It has been incorporated into fluorescent sensors for Mg2+, though it binds Ca2+ and Zn2+ more avidly. Here, the synthesis of a sulfur analogue of APTRA is reported, namely ortho-aminothiophenol-N,N,S-triacetate, referred to as S-APTRA. The binding of this new pentadentate ligand to Zn2+, Ca2+, and Mg2+ has been monitored in buffered aqueous solution by UV absorption spectroscopy. The replacement of the phenolic oxygen of APTRA by a sulfur atom renders S-APTRA capable of binding Zn2+ in a biologically relevant range (Kd = 6.6 ± 0.3 nM) with high selectivity over Mg2+ and Ca2+. The enhanced selectivity for Zn2+ is in line with the principles of “hard and soft acids and bases.” A tetradentate analogue omitting the S-appended carboxylate group, S-APDIA, is also reported. Its lower denticity leads to decreased affinity for Zn2+ (Kd = 8 ± 1 μM). The oxidation of S-APTRA and S-APDIA by m-CPBA leads to the sulfoxides SO-APTRA and SO-APDIA, which bind Zn2+ yet more weakly (Kd = 260 ± 20 mM and 3.6 ± 0.3 mM, respectively). This new family of ligands may prove appealing in the development of new carboxylate-based zinc sensors.
AB - Ortho-aminophenol-N,N,O-triacetate (APTRA) is a pentadentate ligand adopted for the selective binding of Mg2+. It has been incorporated into fluorescent sensors for Mg2+, though it binds Ca2+ and Zn2+ more avidly. Here, the synthesis of a sulfur analogue of APTRA is reported, namely ortho-aminothiophenol-N,N,S-triacetate, referred to as S-APTRA. The binding of this new pentadentate ligand to Zn2+, Ca2+, and Mg2+ has been monitored in buffered aqueous solution by UV absorption spectroscopy. The replacement of the phenolic oxygen of APTRA by a sulfur atom renders S-APTRA capable of binding Zn2+ in a biologically relevant range (Kd = 6.6 ± 0.3 nM) with high selectivity over Mg2+ and Ca2+. The enhanced selectivity for Zn2+ is in line with the principles of “hard and soft acids and bases.” A tetradentate analogue omitting the S-appended carboxylate group, S-APDIA, is also reported. Its lower denticity leads to decreased affinity for Zn2+ (Kd = 8 ± 1 μM). The oxidation of S-APTRA and S-APDIA by m-CPBA leads to the sulfoxides SO-APTRA and SO-APDIA, which bind Zn2+ yet more weakly (Kd = 260 ± 20 mM and 3.6 ± 0.3 mM, respectively). This new family of ligands may prove appealing in the development of new carboxylate-based zinc sensors.
UR - https://www.scopus.com/pages/publications/105004433873
U2 - 10.1021/acs.inorgchem.5c00275
DO - 10.1021/acs.inorgchem.5c00275
M3 - Journal article
C2 - 40331671
SN - 0020-1669
VL - 64
SP - 9509
EP - 9518
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 19
ER -