TY - JOUR
T1 - In silico Docking Analysis for Blocking JUNO‐IZUMO1 Interaction Identifies Two Small Molecules that Block in vitro Fertilization
AU - Stepanenko, Nataliia
AU - Wolk, Omri
AU - Bianchi, Enrica
AU - Wright, Gavin James
AU - Schachter-Safrai, Natali
AU - Makedonski, Kiril
AU - Ouro, Alberto
AU - Ben-Meir, Assaf
AU - Buganim, Yosef
AU - Goldblum, Amiram
N1 - Publisher Copyright:
Copyright © 2022 Stepanenko, Wolk, Bianchi, Wright, Schachter-Safrai, Makedonski, Ouro, Ben-Meir, Buganim and Goldblum.
PY - 2022/4/5
Y1 - 2022/4/5
N2 - Combined hormone drugs are the basis for orally administered contraception. However, they are associated with severe side effects that are even more impactful for women in developing countries, where resources are limited. The risk of side effects may be reduced by non-hormonal small molecules which specifically target proteins involved in fertilization. In this study, we present a virtual docking experiment directed to discover molecules that target the crucial fertilization interactions of JUNO (oocyte) and IZUMO1 (sperm). We docked 913,000 molecules to two crystal structures of JUNO and ranked them on the basis of energy-related criteria. Of the 32 tested candidates, two molecules (i.e., Z786028994 and Z1290281203) demonstrated fertilization inhibitory effect in both an in vitro fertilization (IVF) assay in mice and an in vitro penetration of human sperm into hamster oocytes. Despite this clear effect on fertilization, these two molecules did not show JUNO–IZUMO1 interaction blocking activity as assessed by AVidity-based EXtracellular Interaction Screening (AVEXIS). Therefore, further research is required to determine the mechanism of action of these two fertilization inhibitors.
AB - Combined hormone drugs are the basis for orally administered contraception. However, they are associated with severe side effects that are even more impactful for women in developing countries, where resources are limited. The risk of side effects may be reduced by non-hormonal small molecules which specifically target proteins involved in fertilization. In this study, we present a virtual docking experiment directed to discover molecules that target the crucial fertilization interactions of JUNO (oocyte) and IZUMO1 (sperm). We docked 913,000 molecules to two crystal structures of JUNO and ranked them on the basis of energy-related criteria. Of the 32 tested candidates, two molecules (i.e., Z786028994 and Z1290281203) demonstrated fertilization inhibitory effect in both an in vitro fertilization (IVF) assay in mice and an in vitro penetration of human sperm into hamster oocytes. Despite this clear effect on fertilization, these two molecules did not show JUNO–IZUMO1 interaction blocking activity as assessed by AVidity-based EXtracellular Interaction Screening (AVEXIS). Therefore, further research is required to determine the mechanism of action of these two fertilization inhibitors.
KW - JUNO–IZUMO1 interaction
KW - docking
KW - human sperm penetration assay
KW - in vitro fertilization
KW - non-hormonal contraceptives
UR - http://www.scopus.com/inward/record.url?scp=85128758642&partnerID=8YFLogxK
U2 - 10.3389/fcell.2022.824629
DO - 10.3389/fcell.2022.824629
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C2 - 35478965
AN - SCOPUS:85128758642
SN - 2296-634X
VL - 10
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 824629
ER -