蛋白质S Erlangen突变PROS1c.1904T>C (F635S) 抑制了分泌的作用
Clinical laboratory
|March 12, 2024
概括
蛋白质S Erlangen突变导致严重的蛋白质S缺乏,由于分泌缺陷. 这种突变将蛋白质困在细胞内网膜中,阻止其释放,导致血栓形成.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 生物化学 生物化学
背景情况:
- 一个新的PROS1突变,蛋白质S Erlangen (c.1904T>C,F635S),与严重的蛋白质S (PS) 缺乏和血栓形成有关.
- 人们假设这种缺陷源于PS分泌的缺陷.
研究的目的:
- 为了研究蛋白质S Erlangen突变的潜在分泌缺陷.
- 为了阐明由这种突变引起的PS缺乏症背后的细胞机制.
主要方法:
- 克隆野生类型 (WT) 和突变PROS1 (编码PS) 融合到绿色光蛋白 (GFP).
- 在HEK293T细胞中表达PROS1-GFP结构.
- 使用西斑和共聚焦显微镜分析蛋白质局部化和分泌.
主要成果:
- 与WTPS相比,突变蛋白S (PSF635S) 的分泌量显著降低.
- 该PSF635S-GFP融合蛋白仅局限于内质网膜 (ER).
- 在整个分泌途径中检测到WT PS-GFP,包括ER和Golgi装置.
结论:
- 蛋白S Erlangen突变导致I型PS缺乏症.
- 这种缺陷是由特定的分泌缺陷引起的,将突变蛋白质困在ER中.
更多相关视频
12:21Thermostabilization, Expression, Purification, and Crystallization of the Human Serotonin Transporter Bound to S-citalopram
Published on: November 27, 2016
15.1K
05:48Removal of an Internal Translational Start Site from mRNA While Retaining Expression of the Full-Length Protein
Published on: March 16, 2022
2.6K
相关概念视频
Mutations
82.2K
Overview
82.2K
Leaky Scanning
5.1K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA. Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.1K
Protein Modifications in the RER
5.2K
Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
5.2K
Regulation of Nuclear Protein Sorting
2.4K
Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
2.4K
Translation
14.9K
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...
14.9K
Nonsense-mediated mRNA Decay
10.6K
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,...
10.6K
