Tuning the anion binding properties of lanthanide receptors to discriminate nucleoside phosphates in a sensing array
The development of synthetic receptors for the selective binding and discrimination of anions in water requires an understanding of how anions interact with these synthetic receptors. Molecules designed to differentiate nucleoside phosphate anions (e.g. ATP, ADP, GTP, GDP, UDP) under physiological conditions could underpin exciting new sensing tools for biomedical research and drug discovery, but it is very challenging due to the similarities in anion structure, size and charge. We present a series of lanthanide-based anion receptors and establish key structural elements that impact on nucleoside phosphate anion binding and sensing. Structural evidence of anion binding using X-ray crystallographic and NMR data, supported by DFT calculations indicate the binding modes between the lanthanide complexes and certain phosphoanions, revealing a bidentate (a-, g-) binding mode to ATP. We further use four of the receptors to allow discrimination of eight nucleoside phosphate anions in the first arraybased assay using lanthanide complexes, taking advantage of the multiple emission bands and long emission lifetimes associated with luminescent lanthanide complexes.
Funding
Luminescent Host Molecules for Multisite Recognition of Polyphosphate Anions
Engineering and Physical Sciences Research Council
Find out more...Wellcome Trust (204500/Z/16/Z)
History
School
- Science
Department
- Chemistry
Published in
Chemical ScienceVolume
11Issue
14Pages
3619 - 3628Publisher
Royal Society of Chemistry (RSC)Version
- VoR (Version of Record)
Rights holder
© The authorsPublisher statement
This is an Open Access Article. It is published by Royal Society of Chemistry (RSC) under the Creative Commons Attribution 4.0 Unported Licence (CC BY). Full details of this licence are available at: http://creativecommons.org/licenses/by/4.0/Acceptance date
2020-03-10Publication date
2020-03-11Copyright date
2020ISSN
2041-6520eISSN
2041-6539Publisher version
Language
- en