相关实验视频
Updated: Jan 7, 2026

10:56
Assays for the Degradation of Misfolded Proteins in Cells
Published on: August 28, 2016
12.5K
在神经退行性疾病中,RNA G-quadruplexes介导蛋白质聚合
Tu Chen Guan1, Li Zeng2, Mei Liu3
1National Neuroscience Institute, 11 Jalan Tan Tock Seng, Singapore 308433, Singapore; Key Laboratory of Neuroregeneration, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu 226001, China.
Ageing research reviews
|December 31, 2025
概括
RNA G-四复合体 (rG4s) 调节RNA代谢,并与神经退行性疾病有关. 本研究综合了rG4s如何影响蛋白质聚合,并讨论了针对这些结构的治疗策略.
科学领域:
- 分子生物学分子生物学
- 生物物理学的生物物理.
- 神经科学是一个神经科学.
背景情况:
- RNA G四复合体 (rG4s) 是RNA中稳定的二次结构.
- rG4s 调节各种转录后过程.
- rG4s涉及神经退行性疾病 (NDs),如阿尔茨海默氏症和帕金森病.
研究的目的:
- 通过生物物理,细胞和分子机制合成rG4s如何影响蛋白质聚合.
- 在相分离和聚合路径中强调rG4驱动的扰动.
- 讨论rG4s在ND病原,生物标志物开发和治疗干预中的作用.
主要方法:
- 关于生物物理,细胞和分子机制的文学综合.
- 对rG4参与相位分离和蛋白质聚合的分析.
- 对rG4向治疗策略的审查.
主要成果:
- rG4s有助于NDs中的病态蛋白质聚合.
- rG4s 扰乱相位分离和聚合通路.
- rG4s与ND病原和治疗发展有关.
结论:
- rG4s是RNA代谢的关键调节者,在ND中具有病理作用.
- 针对rG4s,可能是像5-ALA这样的小分子,为神经退行提供了治疗途径.
相关概念视频
Amyloid Fibrils
11.5K
Amyloid fibrils are aggregates of misfolded proteins. Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils.
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
11.5K
Amyloid Fibrils
6.2K
6.2K
Proteins: From Genes to Degradation
14.0K
Within a biological system, the DNA encodes the RNA, and the nucleotide sequence in the RNA further defines the amino acid sequence in the protein. This is referred to as “The Central Dogma of Molecular Biology” - a term coined by Francis Crick. Central dogma is a firm principle in biology that defines the flow of genetic information within any life form. The two fundamental steps in central dogma are - transcription and translation.
Transcription is the synthesis of RNA...
Transcription is the synthesis of RNA...
14.0K
Nonsense-mediated mRNA Decay
11.6K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
11.6K
Nuclear Export of mRNA
8.6K
Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
8.6K
Translation
17.4K
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
Translation Produces the Building Blocks of Life
Proteins are...
17.4K

