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1.
Angew Chem Int Ed Engl ; 61(28): e202205403, 2022 07 11.
Artigo em Inglês | MEDLINE | ID: mdl-35511212

RESUMO

3-Nitrotyrosine (NT) is generated by the action of peroxynitrite and other reactive nitrogen species (RNS), and as a consequence it is accumulated in inflammation-associated conditions. This is particularly relevant in kidney disease, where NT concentration in blood is considerably high. Therefore, NT is a crucial biomarker of renal damage, although it has been underestimated in clinical diagnosis due to the lack of an appropriate sensing method. Herein we report the first fluorescent supramolecular sensor for such a relevant compound: Fluorescence by rotational restriction of tetraphenylethenes (TPE) in a covalent cage is selectively quenched in human blood serum by 3-nitrotyrosine (NT) that binds to the cage with high affinity, allowing a limit of detection within the reported physiological concentrations of NT in chronic kidney disease.


Assuntos
Soro , Tirosina , Humanos , Ácido Peroxinitroso , Espécies Reativas de Nitrogênio , Soro/metabolismo , Tirosina/análogos & derivados , Tirosina/metabolismo
2.
Bioconjug Chem ; 32(8): 1564-1569, 2021 08 18.
Artigo em Inglês | MEDLINE | ID: mdl-34320309

RESUMO

Combining coordination chemistry and peptide engineering offers extraordinary opportunities for developing novel molecular (supra)structures. Here, we demonstrate that the ß-annulus motif is capable of directing the stereoselective assembly of designed peptides containing 2,2'-bipyridine ligands into parallel three-stranded chiral peptide helicates, and that these helicates selectively bind with high affinity to three-way DNA junctions.


Assuntos
DNA/química , Peptídeos/química , Vírus de Plantas/química , Sítios de Ligação , Modelos Moleculares , Conformação de Ácido Nucleico , Estereoisomerismo
3.
J Org Chem ; 84(2): 840-850, 2019 01 18.
Artigo em Inglês | MEDLINE | ID: mdl-30596238

RESUMO

The thiol-Michael addition (TMA) is a powerful methodology to click several fragments together, despite having been underestimated in the synthesis of complex systems for supramolecular chemistry. Herein, a very fast and efficient method has been developed to make covalent molecular capsules by taking advantage of the TMA click reaction. Several scaffolds commonly used in supramolecular chemistry, such as calixarenes, CTV, or cavitands, have been used to quickly obtain covalent cages. Additionally, a ' click&click' procedure has been also developed, by sequential combination of TMA and CuAAC click reaction, as an easy and quick way to build complex molecular structures.

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