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相关概念视频

Protein Kinases and Phosphatases02:54

Protein Kinases and Phosphatases

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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...
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Phosphorylation01:02

Phosphorylation

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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...
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Proteomics01:33

Proteomics

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A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term...
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相关实验视频

Updated: Jul 9, 2025

Oligopeptide Competition Assay for Phosphorylation Site Determination
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Oligopeptide Competition Assay for Phosphorylation Site Determination

Published on: May 18, 2017

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蛋白质基编辑器屏幕用于评估高通量中酸化位点的功能.

Patrick H Kennedy, Amin Alborzian Deh Sheikh, Matthew Balakar

    bioRxiv : the preprint server for biology
    |November 28, 2023
    PubMed
    概括

    研究人员开发了一种新的方法,通过将后翻译修改 (PTM) 与基因表达联系起来,绘制信号通路的地图. 这种方法揭示了成千上万的PTM如何微调细胞功能和转录反应.

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    Identification of Kinase-substrate Pairs Using High Throughput Screening
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    Identification of Kinase-substrate Pairs Using High Throughput Screening

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    Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
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    Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

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    相关实验视频

    Last Updated: Jul 9, 2025

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    09:16

    Oligopeptide Competition Assay for Phosphorylation Site Determination

    Published on: May 18, 2017

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    Identification of Kinase-substrate Pairs Using High Throughput Screening
    11:13

    Identification of Kinase-substrate Pairs Using High Throughput Screening

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    Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
    12:26

    Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

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    科学领域:

    • 蜂信号传输是如何进行的
    • 分子生物学分子生物学
    • 遗传学 遗传学 是一个

    背景情况:

    • 细胞信号传递途径复杂,涉及数千个调节基因表达的转化后修饰 (PTMs).
    • 目前的技术在将PTM连接到基因电路的能力上是有限的.
    • 了解PTM对于破译细胞功能至关重要.

    研究的目的:

    • 开发一种用于映射信号转录网络的新技术.
    • 研究PTMs在T细胞激活和基因表达中的作用.
    • 识别以前未被描述的酸化部位及其功能.

    主要方法:

    • 开发了以PTM为中心的基础编辑与表型选相结合.
    • 利用暂时分辨的光蛋白学来指导屏幕.
    • 将该方法应用于T细胞激活作为模型系统.

    主要成果:

    • 确定了数百个未经研究的酸化部位,影响NFAT转录活性.
    • 发现PHLPP1酸酶的核定位,通过酸化介导,促进NFAT和抑制NFκB活动.
    • 证明特定的酸突变可以微妙地改变基因表达模式.

    结论:

    • 以PTM为中心的基础编辑器选是一个强大的平台,用于在信号通路中剖析PTM功能.
    • 这项技术可以对PTM在细胞调节中的作用进行大规模分析.
    • 这些发现为PTMs复杂的基因表达控制提供了新的见解.