基化酶:人类治疗学的发展概念和影响
Evan D Kelly1, Mark J Ranek2, Manling Zhang3,4
1Department of Cell and Molecular Physiology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, USA;
Annual review of pharmacology and toxicology
|September 25, 2024
概括
固酶 (PDEs) 是细胞信号传递至关重要的酶. 选择性PDE抑制剂对于治疗免疫,心脏和血管疾病至关重要,新疗法正在出现.
科学领域:
- 酵素学和分子生物学 酵素学和分子生物学
- 药理学和药物发现
背景情况:
- 固酶 (PDEs) 是一种酶超级家族,它能水解循环核酸.
- 基质选择性,调节,表达和局部化的关键差异使11个PDE亚家族之间具有信号特异性.
- PDEs在正常细胞功能中起着至关重要的作用,并与各种疾病有关.
研究的目的:
- 审查PDE的结构和功能.
- 检查PDE抑制剂的当前和不断发展的治疗应用.
- 强调在临床环境中利用PDE的机制和创新策略.
主要方法:
- 关于PDE结构,功能和抑制的文献综述.
- 对选择性PDE抑制剂现有临床用途的分析.
- 讨论正在进行的PDE向治疗的临床前和临床研究.
主要成果:
- 选择性PDE抑制剂已经阐明了PDEs在细胞功能中的多样性作用.
- PDEs与免疫,心脏和血管疾病有关.
- 现有的PDE抑制剂在临床上用于特定疾病,正在进行新应用的研究.
结论:
- PDEs是具有显著治疗潜力的必需酶.
- 选择性PDE抑制剂代表了治疗各种疾病的宝贵药物类别.
- 对PDE机制和抑制剂的持续研究有望带来新的治疗进展.
相关概念视频
Protein Kinases and Phosphatases
13.1K
Proteins undergo chemical modifications that trigger changes in the charge, structure, and conformation of the proteins. Phosphorylation, acetylation, glycosylation, nitrosylation, ubiquitination, lipidation, methylation, and proteolysis are various protein modifications that regulate protein activity. Such modifications are usually enzyme-driven.
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
13.1K
Phosphodiester Linkages
99.2K
Overview
Phosphodiester bond forms when a phosphoric acid molecule (H3PO4) links with two hydroxyl groups (–OH) of two other molecules, forming two ester bonds. Two water molecules are released in this process. The phosphodiester bond is commonly found in nucleic acids (DNA and RNA) and plays a critical role in their structure and function.
Phosphodiester Bonds Link Nucleotides Together
DNA and RNA are polynucleotides or long chains of nucleotides that are linked together. A nucleotide is...
Phosphodiester bond forms when a phosphoric acid molecule (H3PO4) links with two hydroxyl groups (–OH) of two other molecules, forming two ester bonds. Two water molecules are released in this process. The phosphodiester bond is commonly found in nucleic acids (DNA and RNA) and plays a critical role in their structure and function.
Phosphodiester Bonds Link Nucleotides Together
DNA and RNA are polynucleotides or long chains of nucleotides that are linked together. A nucleotide is...
99.2K
Phosphorylation
50.1K
The addition or removal of phosphate groups from proteins is the most common chemical modification that regulates cellular processes. These modifications can affect the structure, activity, stability, and localization of proteins within cells as well as their interactions with other proteins.
During phosphorylation, protein kinases transfer the terminal phosphate group of ATP to specific amino acid side chains of substrate proteins. Serine, threonine, and tyrosine are the most commonly...
During phosphorylation, protein kinases transfer the terminal phosphate group of ATP to specific amino acid side chains of substrate proteins. Serine, threonine, and tyrosine are the most commonly...
50.1K
Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors
134
Phosphodiesterase 5 (PDE5) inhibitors are potent enzymes that function to hydrolyze cyclic nucleotides to their corresponding 5' monophosphates. Their unique biochemical properties have been applied in treating Pulmonary Arterial Hypertension (PAH).
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
134
Transducer Mechanism: Enzyme-Linked Receptors
2.4K
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
2.4K
Phosphoinositides and PIPs
8.5K
Phosphoinositides are a group of phospholipids containing a glycerol backbone with two fatty acid chains and a phosphate attached to a myoinositol sugar ring. The inositol head group extends into the cytoplasm, where it is modified by adding phosphate groups to form phosphatidylinositol phosphates or PIPs.
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
Different phosphoinositides are synthesized and recruited on the cytosolic face of the plasma membrane. The localization of specific phosphoinositides concentrated in separate membrane...
8.5K


