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相关概念视频

Chromatin Packaging01:32

Chromatin Packaging

16.7K
Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
16.7K
Nucleosome Remodeling02:54

Nucleosome Remodeling

9.1K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
9.1K
Euchromatin01:01

Euchromatin

6.9K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions take up more dye, appearing darker, while the less-compact areas take up less dye and appear lighter. Based on the compaction level, chromatins are classified into two primary forms – euchromatin and heterochromatin.
Euchromatin is the less dense region of the chromatin and stains lighter. Euchromatin contains histone H3 extensively...
6.9K
Chromatin Immunoprecipitation- ChIP02:36

Chromatin Immunoprecipitation- ChIP

11.1K
Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
11.1K
Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

5.5K
The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
5.5K
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

6.2K
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...
6.2K

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相关实验视频

Updated: Jul 4, 2025

Sequential Salt Extractions for the Analysis of Bulk Chromatin Binding Properties of Chromatin Modifying Complexes
07:41

Sequential Salt Extractions for the Analysis of Bulk Chromatin Binding Properties of Chromatin Modifying Complexes

Published on: October 2, 2017

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显式离子建模预测了染色体组织的物理化学相互作用.

Xingcheng Lin1, Bin Zhang1

  • 1Department of Chemistry, Massachusetts Institute of Technology, Cambridge, United States.

eLife
|January 30, 2024
PubMed
概括

这项研究引入了一个明确的离子模型,以准确预测染色质组织和核细胞核细胞结合强度. 该模型协调实验数据,并预测在生理条件下9kT的结合强度.

科学领域:

  • 生物物理学的生物物理.
  • 分子生物学分子生物学
  • 计算生物学 计算生物学

背景情况:

  • 染色体组织对于细胞功能至关重要,但内在相互作用的作用仍在争论中.
  • 核-核结合强度是一个关键参数,之前的估计差异很大 (214 k T).

研究的目的:

  • 开发一种更准确的染色体组织计算模型.
  • 解决核-核结合强度的实验估计中的差异.
  • 为了研究离子对染色质结构的影响.

主要方法:

  • 开发了一个明确的离子模型,用于残留级粗粒模拟.
  • 进行了大规模的构造性采样和自由能量计算.
  • 与蛋白质-DNA结合和DNA解的实验数据对模型进行了验证.

主要成果:

  • 该模型准确地预测了染色质组织和核体与核体结合的能量.
  • 它解决了单价离子和双价离子对染色质的差异作用.
  • 调和各种不同的实验数据,解释结合强度估计中的差异.
  • 预测生理结合强度为9kT,对链接DNA和基因素存在敏感.
关键词:
30纳米的纤维纤维是30纳米的.染色体的折叠 染色体折叠粗粒度建模粗粒度建模显式离子 显式离子分子生物物理学分子生物物理学没有,没有,没有.结构生物学结构生物学

更多相关视频

Genome-wide Mapping of Drug-DNA Interactions in Cells with COSMIC Crosslinking of Small Molecules to Isolate Chromatin
10:05

Genome-wide Mapping of Drug-DNA Interactions in Cells with COSMIC Crosslinking of Small Molecules to Isolate Chromatin

Published on: January 20, 2016

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Chromatin Extraction from Frozen Chimeric Liver Tissue for Chromatin Immunoprecipitation Analysis
09:26

Chromatin Extraction from Frozen Chimeric Liver Tissue for Chromatin Immunoprecipitation Analysis

Published on: March 23, 2021

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相关实验视频

Last Updated: Jul 4, 2025

Sequential Salt Extractions for the Analysis of Bulk Chromatin Binding Properties of Chromatin Modifying Complexes
07:41

Sequential Salt Extractions for the Analysis of Bulk Chromatin Binding Properties of Chromatin Modifying Complexes

Published on: October 2, 2017

8.4K
Genome-wide Mapping of Drug-DNA Interactions in Cells with COSMIC Crosslinking of Small Molecules to Isolate Chromatin
10:05

Genome-wide Mapping of Drug-DNA Interactions in Cells with COSMIC Crosslinking of Small Molecules to Isolate Chromatin

Published on: January 20, 2016

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Chromatin Extraction from Frozen Chimeric Liver Tissue for Chromatin Immunoprecipitation Analysis
09:26

Chromatin Extraction from Frozen Chimeric Liver Tissue for Chromatin Immunoprecipitation Analysis

Published on: March 23, 2021

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结论:

  • 物理化学相互作用对染色体相位行为和核组织有显著的贡献.
  • 显式离子模型为研究色素动态提供了一个强大的框架.
  • 准确的建模对于理解基因组组织的复杂调节至关重要.