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相关概念视频

Chromatin Structure Regulates pre-mRNA Processing02:41

Chromatin Structure Regulates pre-mRNA Processing

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In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
The chromatin structure, especially...
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Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

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Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
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Regulated Protein Degradation02:58

Regulated Protein Degradation

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It is vital to regulate the activity of enzymatic as well as non-enzymatic proteins inside the cell. This can be achieved either through creating a balance between their rate of synthesis and degradation or regulating the intrinsic activity of the protein. Both these regulation mechanisms play an essential role in the normal functioning of cells.
Protein degradation plays two important roles in the cells. It helps to protect cells from misfolded or damaged proteins before they lead to a...
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Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

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Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
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Turnover Number and Catalytic Efficiency01:19

Turnover Number and Catalytic Efficiency

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The turnover number of an enzyme is the maximum number of substrate molecules it can transform per unit time. Turnover numbers for most enzymes range from 1 to 1000 molecules per second. Catalase has the known highest turnover number, capable of converting up to 2.8×106 molecules of hydrogen peroxide into water and oxygen per second. Lysozyme has the lowest known turnover number of half a molecule per second.
Chymotrypsin is a pancreatic enzyme that breaks down proteins during digestion....
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Catalytically Perfect Enzymes01:07

Catalytically Perfect Enzymes

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The theory of catalytically perfect enzymes was first proposed by W.J. Albery and J. R. Knowles in 1976. These enzymes catalyze biochemical reactions at high-speed. Their catalytic efficiency values range from 108-109 M-1s-1. These enzymes are also called 'diffusion-controlled' as the only rate-limiting step in the catalysis is that of the substrate diffusion into the active site. Examples include triose phosphate isomerase, fumarase, and superoxide dismutase.
 
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相关实验视频

Updated: Feb 7, 2026

Sigma's Non-specific Protease Activity Assay - Casein as a Substrate
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Sigma's Non-specific Protease Activity Assay - Casein as a Substrate

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在S9D蛋白酶中,二分化,催化调节和基质选择性的结构基础.

Jacqueline J Ehrlich, Pratyush Routray, Louis Enns

    bioRxiv : the preprint server for biology
    |February 6, 2026
    PubMed
    概括

    研究人员揭示了一种植物S9D蛋白酶的结构,即质细胞谷氨基末酶 (CGEP). 这种蛋白酶使用独特的链循环门机制进行调节,并表现出对谷氨酸酸的强烈偏好,进步了蛋白酶的理解.

    科学领域:

    • 蛋白质酶是一种蛋白质酶.
    • 结构生物学 结构生物学
    • 植物生物化学 植物生物化学

    背景情况:

    • S9蛋白酶对于整个生命中的蛋白质加工至关重要.
    • S9D亚家族蛋白酶的结构和机制基础在很大程度上是未知的.

    研究的目的:

    • 为了确定一个S9D蛋白酶的高分辨率冷EM结构,质细胞谷氨基内酶 (CGEP).
    • 阐明CGEP活动和基质特异性的结构和机制基础.

    主要方法:

    • 高分辨率冷电子显微镜 (cryo-EM) 的CGEP.
    • 植物和细菌中的蛋白质表达.
    • 结构分析和突变发生研究.

    主要成果:

    • 通过防水和域间β-片相互作用,CGEP形成稳定的二元体.
    • 一个链循环作为一个固态门,调节基板的访问和催化活动.
    • CGEP 保持完整的催化三合一,由链环门控制,而不是催化干扰.
    • 链环中的一个保留的口袋解释了CGEP对谷氨酸的强烈偏好.

    结论:

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  • 这项研究揭示了S9D蛋白酶的独特调节机制,涉及链环门.
  • 这些发现为了解CGEP的基质选择性和二元化提供了一个结构框架.
  • 促进了对蛋白酶多样性的理解,并为蛋白酶工程开辟了道路.