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Functional proteomics has allowed us to formulate a comprehensive understanding of receptors’ structure, a mechanism for the macromolecular basis of receptor heteromerization and define heteromers formation (e.g. Adenosine A2A-Dopamine D2, Cannabinoid CB1-Dopamine D2 and NMDA NR1-Dopamine D1) at the molecular level. Through the study of noncovalent interactions, we have also elucidated the mechanism of NMDA mediated dynorphin neurotoxicity and designed a decoy peptide that takes into account the structure of its target.
Functional proteomics has allowed us to formulate a comprehensive understanding of receptors’ structure, a mechanism for the macromolecular basis of receptor heteromerization and define heteromers formation (e.g. Adenosine A2A-Dopamine D2, Cannabinoid CB1-Dopamine D2 and NMDA NR1-Dopamine D1) at the molecular level. Through the study of noncovalent interactions, we have also elucidated the mechanism of NMDA mediated dynorphin neurotoxicity and designed a decoy peptide that takes into account the structure of its target.
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论文共 257 篇作者统计合作学者相似作者
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Benjamin L. Oyler, Jeferson A. Valencia-Dávila,Eirini Moysi, Adam Molyvdas,Kalliopi Ioannidou,Kylie March,David Ambrozak,Laurence De Leval,Giulia Fabozzi,Amina S. Woods,Richard A. Koup,Constantinos Petrovas
biorxiv(2023)
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