Research progress on phosphatidylinositol 4-kinase inhibitors

被引:4
|
作者
Li, Gang [1 ]
Wu, Yanting [1 ,2 ]
Zhang, Yali [1 ]
Wang, Huamin [1 ]
Li, Mengjie [1 ]
He, Dengqin [3 ]
Guan, Wen [1 ]
Yao, Hongliang [1 ]
机构
[1] Guangdong Acad Sci, Inst Zool, Guangdong Key Lab Anim Conservat & Resource Utiliz, Guangdong Publ Lab Wild Anim Conservat & Utilizat, Guangzhou 510260, Guangdong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Clearwater Bay, Hong Kong 999077, Peoples R China
[3] Wuyi Univ, Sch Biotechnol & Hlth Sci, 22 Dongchengcun, Jiangmen 529020, Guangdong, Peoples R China
关键词
PI4K; PI4P; Malaria; Alzheimer; Tumor; Nervous system disease; NEURONAL CALCIUM SENSOR-1; LIPID KINASE PI4KIII-BETA; SMALL-MOLECULE INHIBITORS; ELONGATION-FACTOR EEF1A2; TRANS-GOLGI NETWORK; PLASMA-MEMBRANE; II-ALPHA; STRUCTURAL BASIS; KEY COMPONENT; NONVESICULAR TRAFFICKING;
D O I
10.1016/j.bcp.2023.115993
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Phosphatidylinositol 4-kinases (PI4Ks) could phosphorylate phosphatidylinositol (PI) to produce phosphatidylinositol 4-phosphate (PI4P) and maintain its metabolic balance and location. PI4P, the most abundant mono-phosphate inositol in eukaryotic cells, is a precursor of higher phosphoinositols and an essential substrate for the PLC/PKC and PI3K/Akt signaling pathways. PI4Ks regulate vesicle transport, signal transduction, cytokinesis, and cell unity, and are involved in various physiological and pathological processes, including infection and growth of parasites such as Plasmodium and Cryptosporidium, replication and survival of RNA viruses, and the development of tumors and nervous system diseases. The development of novel drugs targeting PI4Ks and PI4P has been the focus of the research and clinical application of drugs, especially in recent years. In particular, PI4K inhibitors have made great progress in the treatment of malaria and cryptosporidiosis. We describe the biological characteristics of PI4Ks; summarize the physiological functions and effector proteins of PI4P; and analyze the structural basis of selective PI4K inhibitors for the treatment of human diseases in this review. Herein, this review mainly summarizes the developments in the structure and enzyme activity of PI4K inhibitors.
引用
收藏
页数:16
相关论文
共 50 条
  • [41] Purification and characterization of a type II phosphatidylinositol 4-kinase from rat spleen and comparison with a PtdIns 4-kinase from lymphocytes
    Verghese, M
    Fernandis, AZ
    Subrahmanyam, G
    INDIAN JOURNAL OF BIOCHEMISTRY & BIOPHYSICS, 1999, 36 (01): : 1 - 9
  • [42] Fluorescent Inhibitors as Tools To Characterize Enzymes: Case Study of the Lipid Kinase Phosphatidylinositol 4-Kinase IIIβ (PI4KB)
    Humpolickova, Jana
    Mejdrova, Ivana
    Matousova, Marika
    Nencka, Radim
    Boura, Evzen
    JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (01) : 119 - 127
  • [43] PHOSPHATIDYLINOSITOL 4-KINASE IS A COMPONENT OF GLUCOSE TRANSPORTER (GLUT 4)-CONTAINING VESICLES
    DELVECCHIO, RL
    PILCH, PF
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1991, 266 (20) : 13278 - 13283
  • [44] Molecular insights into the membrane-associated phosphatidylinositol 4-kinase IIα
    Zhou, Qiangjun
    Li, Jiangmei
    Yu, Hang
    Zhai, Yujia
    Gao, Zhen
    Liu, Yanxin
    Pang, Xiaoyun
    Zhang, Lunfeng
    Schulten, Klaus
    Sun, Fei
    Chen, Chang
    NATURE COMMUNICATIONS, 2014, 5
  • [45] A MONOCLONAL-ANTIBODY DISTINGUISHES 2 TYPES OF PHOSPHATIDYLINOSITOL 4-KINASE
    ENDEMANN, GC
    GRAZIANI, A
    CANTLEY, LC
    BIOCHEMICAL JOURNAL, 1991, 273 : 63 - 66
  • [47] SEPARATION AND IDENTIFICATION OF 2 PHOSPHATIDYLINOSITOL 4-KINASE ACTIVITIES IN BOVINE UTERUS
    LI, YS
    PORTER, FD
    HOFFMAN, RM
    DEUEL, TF
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 160 (01) : 202 - 209
  • [48] FUNCTIONAL ANALYSIS OF THE ANTIMALARIAL TARGET PLASMODIUM FALCIPARUM PHOSPHATIDYLINOSITOL 4-KINASE
    Sternberg, Anna R.
    Hassett, Matthew R.
    Roepe, Paul D.
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2019, 101 : 273 - 273
  • [49] Association of protein kinase c μ with type II phosphatidylinositol 4-kinase and type I phosphatidylinositol-4-phosphate 5-kinase
    Nishikawa, K
    Toker, A
    Wong, K
    Marignani, PA
    Johannes, FJ
    Cantley, LC
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (36) : 23126 - 23133
  • [50] An In Silico Approach for Targeting Plasmodium Phosphatidylinositol 4-Kinase to Eradicate Malaria
    Chaudhary, Kamal Kumar
    Gupta, Sarvesh Kumar
    Mishra, Nidhi
    ADVANCED COMPUTING AND COMMUNICATION TECHNOLOGIES, 2016, 452 : 279 - 287