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A polyaromatic receptor with high androgen affinity

Biological receptors distinguish and bind steroid sex hormones, e.g., androgen-, progestogen-, and estrogen-type hormones, with high selectivity. To date, artificial molecular receptors have been unable to discriminate between these classes of biosubstrates. Here, we report that an artificial polyar...

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Autores principales: Yamashina, Masahiro, Tsutsui, Takahiro, Sei, Yoshihisa, Akita, Munetaka, Yoshizawa, Michito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474769/
https://www.ncbi.nlm.nih.gov/pubmed/31016239
http://dx.doi.org/10.1126/sciadv.aav3179
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author Yamashina, Masahiro
Tsutsui, Takahiro
Sei, Yoshihisa
Akita, Munetaka
Yoshizawa, Michito
author_facet Yamashina, Masahiro
Tsutsui, Takahiro
Sei, Yoshihisa
Akita, Munetaka
Yoshizawa, Michito
author_sort Yamashina, Masahiro
collection PubMed
description Biological receptors distinguish and bind steroid sex hormones, e.g., androgen-, progestogen-, and estrogen-type hormones, with high selectivity. To date, artificial molecular receptors have been unable to discriminate between these classes of biosubstrates. Here, we report that an artificial polyaromatic receptor preferentially binds a single molecule of androgenic hormones, known as “male” hormones (indicated with m), over progestogens and estrogens, known as “female” hormones (indicated with f), in water. Competitive experiments established the binding selectivity of the synthetic receptor for various sex hormones to be testosterone (m) > androsterone (m) >> progesterone (f) > β-estradiol (f) > pregnenolone (f) > estriol (f). These bindings are driven by the hydrophobic effect, and the observed selectivity arises from multiple CH-π contacts and hydrogen-bonding interactions in the semirigid polyaromatic cavity. Furthermore, micromolar fluorescence detection of androgen was demonstrated using the receptor containing a fluorescent dye in water.
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spelling pubmed-64747692019-04-23 A polyaromatic receptor with high androgen affinity Yamashina, Masahiro Tsutsui, Takahiro Sei, Yoshihisa Akita, Munetaka Yoshizawa, Michito Sci Adv Research Articles Biological receptors distinguish and bind steroid sex hormones, e.g., androgen-, progestogen-, and estrogen-type hormones, with high selectivity. To date, artificial molecular receptors have been unable to discriminate between these classes of biosubstrates. Here, we report that an artificial polyaromatic receptor preferentially binds a single molecule of androgenic hormones, known as “male” hormones (indicated with m), over progestogens and estrogens, known as “female” hormones (indicated with f), in water. Competitive experiments established the binding selectivity of the synthetic receptor for various sex hormones to be testosterone (m) > androsterone (m) >> progesterone (f) > β-estradiol (f) > pregnenolone (f) > estriol (f). These bindings are driven by the hydrophobic effect, and the observed selectivity arises from multiple CH-π contacts and hydrogen-bonding interactions in the semirigid polyaromatic cavity. Furthermore, micromolar fluorescence detection of androgen was demonstrated using the receptor containing a fluorescent dye in water. American Association for the Advancement of Science 2019-04-19 /pmc/articles/PMC6474769/ /pubmed/31016239 http://dx.doi.org/10.1126/sciadv.aav3179 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Yamashina, Masahiro
Tsutsui, Takahiro
Sei, Yoshihisa
Akita, Munetaka
Yoshizawa, Michito
A polyaromatic receptor with high androgen affinity
title A polyaromatic receptor with high androgen affinity
title_full A polyaromatic receptor with high androgen affinity
title_fullStr A polyaromatic receptor with high androgen affinity
title_full_unstemmed A polyaromatic receptor with high androgen affinity
title_short A polyaromatic receptor with high androgen affinity
title_sort polyaromatic receptor with high androgen affinity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474769/
https://www.ncbi.nlm.nih.gov/pubmed/31016239
http://dx.doi.org/10.1126/sciadv.aav3179
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