A polyaromatic receptor with high androgen affinity

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Presentation transcript:

A polyaromatic receptor with high androgen affinity by Masahiro Yamashina, Takahiro Tsutsui, Yoshihisa Sei, Munetaka Akita, and Michito Yoshizawa Science Volume 5(4):eaav3179 April 19, 2019 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).

Fig. 1 Structures of steroid sex hormones, a natural androgen receptor, and a synthetic receptor. Structures of steroid sex hormones, a natural androgen receptor, and a synthetic receptor. (A) Tetracyclic framework of steroid sex hormones. (B) Crystal structures of a human androgen receptor (6, left) and synthetic receptor 1 (right) shown at the same scale. The binding pocket and cavity are highlighted in yellow. (C) Polyaromatic receptor 1 used here and space-filling representation of the core framework (based on the crystal structure). (D) Representative male hormone, testosterone (2a), and female hormones, progesterone (3a) and β-estradiol (4a). Masahiro Yamashina et al. Sci Adv 2019;5:eaav3179 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).

Fig. 2 Selective binding of testosterone by receptor 1 from mixtures. Selective binding of testosterone by receptor 1 from mixtures. (A) Schematic representation of the selective binding of testosterone (2a) by receptor 1 from a mixture of 2a, progesterone (3a), and β-estradiol (4a) (1:1:1 or 1:100:100 ratio) in water. 1H NMR spectra (500 MHz, D2O) of (B) receptor 1 and (C) products obtained from an equimolar mixture of 2a, 3a, and 4a in the presence of 1 at 60°C for 10 min (gray square, 1•3a) and (D) 1•2a. (E) Changes of the 1H NMR chemical shifts (Δδ in ppm) of 2a upon encapsulation by 1. (F) ESI-TOF MS spectrum (H2O, room temperature) of 1•2a. Masahiro Yamashina et al. Sci Adv 2019;5:eaav3179 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).

Fig. 3 X-ray crystal structure of 1’•2a. X-ray crystal structure of 1’•2a. (A) Space-filling (for 2a) and cylindrical (for 1’) representation and (B) space-filling representation (the peripheral substituents of 1’ are replaced by hydrogen atoms for clarity). (C) Highlighted positions of 2a inside the polyaromatic shell of 1’ (three different views). (D) Highlighted host-guest interactions of 1’•2a in the cavity (blue, orange, and red dashed lines are CH-π, OH-π, and hydrogen-bonding interactions, respectively). Masahiro Yamashina et al. Sci Adv 2019;5:eaav3179 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).

Fig. 4 Binding affinity of receptor 1 toward male hormones. Binding affinity of receptor 1 toward male hormones. (A) Schematic representation of the binding preference of receptor 1 toward male hormones 2a to 2e in water. (B) 1H NMR spectra (500 MHz, D2O, room temperature) of 1•2a (top), 1•2c (middle), and the product (bottom) obtained from an equimolar mixture of 2a and 2c with 1 (blue circle, 1•2a; pale blue square, 1•2c). (C) 1H NMR spectra (500 MHz, D2O, room temperature) of 1•2a (top), 1•2d (middle), and the product (bottom) obtained from an equimolar mixture of 2a and 2d with 1 (blue circle, 1•2a; pale blue triangle, 1•2d). Binding preference of 1 toward (D) 2a and methyltestosterone (5a) and (E) 2d and adrenosterone (5b) in water. Masahiro Yamashina et al. Sci Adv 2019;5:eaav3179 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).

Fig. 5 Binding affinity of receptor 1 toward female hormones. Binding affinity of receptor 1 toward female hormones. (A) Schematic representation of the binding preference of receptor 1 toward female hormones 3a to 3c and 4a to 4c in water. 1H NMR spectra (500 MHz, D2O, room temperature) of products obtained from equimolar mixtures of (B) 2e and 3a, (C) 3a and 4a, and (D) 4a and 4c with 1. (E) Binding preference of 1 toward 3b and 5α-androstane (5c) in water. Masahiro Yamashina et al. Sci Adv 2019;5:eaav3179 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).

Fig. 6 Fluorescent detection of testosterone by receptor-dye complex 1•6. Fluorescent detection of testosterone by receptor-dye complex 1•6. (A) Schematic representation of nanogram-scale fluorescent detection of male hormone 2a using one drop of an aqueous 1•6 solution (8 μM) and their photographs (λex = 356 nm) on a petri dish. (B) Fluorescence spectra (room temperature, λex = 423 nm) of a H2O solution of 1•6 (78 μM, 0.5 ml) before and after addition of 2a (45 nmol) and their photographs (λex = 356 nm). Masahiro Yamashina et al. Sci Adv 2019;5:eaav3179 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).