Structural studies of serotonin receptor family

被引:9
作者
Parajulee, Apeksha [1 ]
Kim, Kuglae [1 ]
机构
[1] Yonsei Univ, Coll Pharm, Dept Pharm, Incheon 21983, South Korea
基金
新加坡国家研究基金会;
关键词
GPCR; Neurotransmitter; Orthosteric binding sites; Sero-tonin; Signaling mechanism; CRYSTAL-STRUCTURE; 5-HT2A; BINDING; RECOGNITION; ACTIVATION; INSIGHTS;
D O I
10.5483/BMBRep.2023-0147
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Serotonin receptors, also known as 5-HT receptors, belong to the G protein-coupled receptors (GPCRs) superfamily. They mediate the effects of serotonin, a neurotransmitter that plays a key role in a wide range of functions including mood regulation, cognition and appetite. The functions of serotonin are mediated by a family of 5-HT receptors including 12 GPCRs belonging to six major families: 5-HT1, 5-HT2, 5-HT4, 5-HT5, 5-HT6 and 5-HT7. Despite their distinct characteristics and functions, these receptors' subtypes share common structural features and signaling mechanisms. Understanding the structure, functions and pharmacology of the serotonin receptor family is essential for unraveling the complexities of serotonin signaling and developing targeted therapeutics for neuropsychiatric disorders. However, developing drugs that selectively target specific receptor subtypes is challenging due to the structural similarities in their orthosteric binding sites. This review focuses on the recent advancements in the structural studies of 5-HT receptors, highlighting the key structural features of each subtype and shedding light on their potential as targets for mental health and neurological disorders (such as depression, anxiety, schizophrenia, and migraine) drugs. [BMB Reports 2023; 56(10):
引用
收藏
页码:527 / 536
页数:10
相关论文
共 50 条
  • [41] Structural Position Correlation Analysis (SPCA) for Protein Family
    Du, Qi-Shi
    Meng, Jian-Zong
    Wang, Cheng-Hua
    Long, Si-Yu
    Huang, Ri-Bo
    [J]. PLOS ONE, 2011, 6 (12):
  • [42] Structural studies of the spliceosome: Bridging the gaps
    Tholen, J.
    Galej, W. P.
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2022, 77
  • [43] Structural basis of ligand recognition and activation of the histamine receptor family
    Zhang, Xuan
    Liu, Guibing
    Zhong, Ya-Ni
    Zhang, Ru
    Yang, Chuan-Cheng
    Niu, Canyang
    Pu, Xuanyu
    Sun, Jingjing
    Zhang, Tianyao
    Yang, Lejin
    Zhang, Chao
    Li, Xiu
    Shen, Xinyuan
    Xiao, Peng
    Sun, Jin-Peng
    Gong, Weimin
    [J]. NATURE COMMUNICATIONS, 2024, 15 (01)
  • [44] Structural basis of ? chain family receptor sharing at the membrane level
    Cai, Tiantian
    Capello, Rachel Lenoir
    Pi, Xiong
    Wu, Hao
    Chou, James J. J.
    [J]. SCIENCE, 2023, 381 (6657) : 569 - 576
  • [45] Structural Stringency and Optimal Nature of Cholesterol Requirement in the Function of the Serotonin1A Receptor
    Parijat Sarkar
    Md. Jafurulla
    Sukanya Bhowmick
    Amitabha Chattopadhyay
    [J]. The Journal of Membrane Biology, 2020, 253 : 445 - 457
  • [46] Structural Insight into G Protein-Coupled Receptor Signaling Efficacy and Bias between Gs and β-Arrestin
    Picard, Louis-Philippe
    Schonegge, Anne-Marie
    Bouvier, Michel
    [J]. ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE, 2019, 2 (03) : 148 - 154
  • [47] STUDIES ON THE ACTIVATION MECHANISMS OF GUANYLYL CYCLASE BY SEROTONIN, PROBABLY THROUGH A NOVEL SUBTYPE OF SEROTONIN RECEPTOR (5-HTGC)
    TOHDA, M
    IMAIZUMI, R
    SEKIYA, A
    ITOH, N
    NOMURA, Y
    [J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 1995, 18 (08) : 1072 - 1075
  • [48] Human Serotonin 5-HT2C G Protein-Coupled Receptor Homology Model from the β2 Adrenoceptor Structure: Ligand Docking and Mutagenesis Studies
    Cordova-Sintjago, Tania
    Villa, Nancy
    Canal, Clinton
    Booth, Raymond
    [J]. INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2012, 112 (01) : 140 - 149
  • [49] Structural analysis of the BisI family of modification dependent restriction endonucleases
    Szafran, Katarzyna
    Rafalski, Dominik
    Skowronek, Krzysztof
    Wojciechowski, Marek
    Kazrani, Asgar Abbas
    Gilski, Miroslaw
    Xu, Shuang-yong
    Bochtler, Matthias
    [J]. NUCLEIC ACIDS RESEARCH, 2024, 52 (15) : 9103 - 9118
  • [50] Structural Determinants for the Binding of Morphinan Agonists to the μ-Opioid Receptor
    Cong, Xiaojing
    Campomanes, Pablo
    Kless, Achim
    Schapitz, Inga
    Wagener, Markus
    Koch, Thomas
    Carloni, Paolo
    [J]. PLOS ONE, 2015, 10 (08):