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Catenins01:23

Catenins

2.6K
Catenins are characterized by multiple binding domains and dynamic structures that allow them to function as linker proteins in cell junction complexes. All catenins, except α-catenin, contain a characteristic protein sequence called the armadillo repeat and are therefore also called armadillo proteins.
Catenins in Cell Junctions
Catenins bind to cell adhesion molecules such as cadherins and link them to different cytoskeletal proteins depending on the type of cell junction. At the...
2.6K
Mechanisms of Membrane Domain Formation00:59

Mechanisms of Membrane Domain Formation

3.5K
Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
3.5K
Structure of Cadherins01:25

Structure of Cadherins

4.0K
The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins”   is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This...
4.0K
Nucleoid01:24

Nucleoid

448
The nucleoid represents a structurally and functionally distinct region within prokaryotic cells, where the cell's DNA and associated proteins are housed. Unlike eukaryotic cells, prokaryotes lack a membrane-bound nucleus, and the nucleoid facilitates the organization and accessibility of the genetic material within this constraint. The DNA in most bacteria and archaea exists as a single, circular, double-stranded molecule that is highly compacted through supercoiling and interactions with...
448
DNA Packaging00:58

DNA Packaging

109.1K
Overview
109.1K
The Nucleosome02:33

The Nucleosome

17.7K
DNA in a human cell is almost 2m long and it is packed inside a tiny nucleus that is only a few microns in diameter. The level of compaction of DNA inside the nucleus is astonishing. It is organized into several sequentially higher levels of compaction to fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
DNA is wound twice around a protein complex called histone core, that consist of 8 histone proteins. This complex...
17.7K

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Updated: Nov 6, 2025

Gene-therapy Inspired Polycation Coating for Protection of DNA Origami Nanostructures
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Gene-therapy Inspired Polycation Coating for Protection of DNA Origami Nanostructures

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カチオンはDNAナノ構造の膜結合と機能を調節する

Diana Morzy1, Roger Rubio-Sánchez1, Himanshu Joshi2

  • 1Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge CB3 0HE, United Kingdom.

Journal of the American Chemical Society
|May 7, 2021
PubMed
まとめ

カチオンはDNAナノ構造と脂質膜の相互作用を媒介し,合成生物学とナノ医療における応用のための複合化に影響を与えます. これらの静電力を理解することで,DNA-脂質組成と新しいナノデバイスの開発を正確に制御することができます.

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Stable DNA Motifs, 1D and 2D Nanostructures Constructed from Small Circular DNA Molecules
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Stable DNA Motifs, 1D and 2D Nanostructures Constructed from Small Circular DNA Molecules

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DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications
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DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications

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関連する実験動画

Last Updated: Nov 6, 2025

Gene-therapy Inspired Polycation Coating for Protection of DNA Origami Nanostructures
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Gene-therapy Inspired Polycation Coating for Protection of DNA Origami Nanostructures

Published on: January 19, 2019

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Stable DNA Motifs, 1D and 2D Nanostructures Constructed from Small Circular DNA Molecules
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DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications
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DNA Origami-Mediated Substrate Nanopatterning of Inorganic Structures for Sensing Applications

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科学分野:

  • バイオ物理学
  • ナノテクノロジー
  • 合成生物学

背景:

  • 核酸と脂質の相互作用は,分子生物学,バイオテクノロジー,ナノ医学にとって根本的なものです.
  • 静電力はこれらの相互作用を支配するが,脂質の多様性と複雑な条件のために未熟である.

研究 の 目的:

  • ジウテリオン性脂質膜とDNAナノ構造の間の静電相互作用を調査する.
  • DNA-脂質複合をプログラムし,膜活性ナノデバイスを設計する方法を特定する.

主な方法:

  • 生理学的に関連するカチオンを用いて相互作用を研究した.
  • 脂質相とイオン値の影響を分析した.
  • 液体とゲル相の脂質二層へのDNA粘着を調査した.

主要な成果:

  • 二重カチオンは核酸とゲル相の脂質二層を橋渡しする.
  • カチオンは,液相膜へのDNA粘着に不可欠であり,水害性DNAの改変でも必要である.
  • 制御されたDNAナノ構造の付着は,水害性と電荷を調節する.

結論:

  • 脂質相とイオンバレンシーは,DNA-脂質の静電相互作用を決定的に影響する.
  • これらの発見は,DNA-脂質複合体と生物模倣ナノデバイスを設計するための新しい戦略を提供します.
  • イオン調節されたDNAベースの合成酵素構造を証明した.