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相关概念视频

Positive Regulator Molecules02:39

Positive Regulator Molecules

7.0K
Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
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Positive Regulator Molecules01:45

Positive Regulator Molecules

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To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
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Negative Regulator Molecules01:23

Negative Regulator Molecules

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Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
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Anaphase Promoting Complex00:50

Anaphase Promoting Complex

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The stepwise destruction of specific proteins is necessary for the progression and completion of the cell cycle. Such proteins are ubiquitinated by ubiquitin ligases and then subsequently destroyed by the proteasome. The SCF (Skp1/Cullin/F-box) and the anaphase-promoting complex (APC) are two important ubiquitin ligases involved in cell cycle progression. While SCF is active throughout the cell cycle, APC gets activated during metaphase to anaphase transition. Cdc20 or Cdh1 binds to APC and...
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Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

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The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
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Separation of Sister Chromatids02:17

Separation of Sister Chromatids

4.6K
At the transition from prophase to metaphase, there is a reduction in cohesion along the chromosomal arms, resulting in the resolution of sister chromatids. However, residual cohesin connections remain to hold the sister chromatids together until the transition from metaphase to anaphase. The residual connection prevents any premature separation of sister chromatids, blocking the risks of aneuploidy within the daughter cells.
At the onset of anaphase, separase, a proteolytic enzyme, is...
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Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors
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佩普5-Cpp,一种由环素D2衍生的抗菌剂.

Bianca Silva Souto1,2,3, Vitória Stephani Hasbahr1, Bárbara Ribeiro Lourenço da Silva1

  • 1Applied Toxinology Laboratory, Butantan Institute, Rua Rudolf Virchow 250, Butantã, São Paulo 05345-040, SP, Brazil.

Molecules (Basel, Switzerland)
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PubMed
概括
此摘要是机器生成的。

抗微生物Pep5-Cpp及其衍生物显示出对抗细菌和真菌的潜力,具有选择性活性和低毒性. 对于药理学应用,支持进一步开发.

关键词:
这是Pep5-Cpppp.抗微生物类的抗微生物.阴离子酸是什么?

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科学领域:

  • 微生物学 微生物学
  • 酸科学 酸科学
  • 抗菌研究 抗菌研究

背景情况:

  • 皮体研究发现了抗瘤Pep5.5.
  • 将Pep5与载体 (Cpp) 结合,产生了抗菌潜力.

研究的目的:

  • 评估Pep5-Cpp及其衍生物 (ΔC3-Pep5-Cpp, ΔN-Pep5-Cpp) 的抗菌活性.
  • 研究它们的作用机制.

主要方法:

  • 最低抑制度 (MIC) 对*黄金葡萄球菌*,*白杆菌*和*黑色菌*进行测定.
  • DNA相互作用研究,光测试,生物膜抑制测试,微生物杀伤性测试和血液溶解测试.

主要成果:

  • 5-Cpp和衍生品对测试的微生物显示了不同的MIC值.
  • 佩普5-Cpp与黄金的DNA相互作用,并增加了它的光.
  • ΔC3-Pep5-Cpp 抑制了生物膜的形成 (>50%).
  • 体显示有选择性的杀菌活性,并且在MIC值下没有显著的血液溶解.

结论:

  • 5-Cpp及其衍生物具有显著的抗微生物潜力和选择性.
  • 这些发现支持这些的未来药理发展.