表面密度グラデーションで組み立てられたDNAポリマーの集合的構成
Gabriel Shemer1, Yahel Atsmon, Eyal Karzbrun
1Department of Materials and Interfaces, Weizmann Institute of Science, Rehovot 76100, Israel.
Journal of the American Chemical Society
|February 17, 2012
まとめ
濃厚二鎖DNA (dsDNA) ポリマーフェーズが研究されました. dsDNA密度は早期に飽和し,エントロピーと排除された体積の相互作用による集団的伸縮を明らかにします.
科学分野:
- バイオフィジックス 生物物理学
- ポリマー物理学 ポリマー物理学
- 分子生物学は分子生物学である.
背景:
- 密度の高いDNAポリマー相を理解することは,細胞のプロセスにとって極めて重要です.
- 以前の研究では,高密度でのDNAの行動を調査する方法がありませんでした.
研究 の 目的:
- 密度の高い二重鎖DNA (dsDNA) のポリマー相の振る舞いを調査する.
- dsDNAにおける集団的ストレッチの発生を特定する.
主な方法:
- 光化学的インターフェイス上の結合部位の連続密度グラデーションの製造.
- evanescent fluorescence を用いて dsDNA の占有および拡張を測定する.
主要な成果:
- dsDNA密度は,利用可能な結合部位のほんの一部を占めてから飽和する.
- 飽和点は,集団的なdsDNAの伸縮の始まりを示しています.
- ストレッチは,エントロピーと排除された体積の相互作用のバランスをとる結果である.
結論:
- この研究は,密度の高いdsDNA区画を調査するための新しい方法論を提示しています.
- 高密度でDNAを制御する物理的な相互作用に関する重要な洞察を明らかにします.
関連する概念動画
DNA Packaging
Overview
DNA as a Genetic Template
Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
Nucleic Acid Structure
The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms a 5′ to 3′ phosphodiester linkage.
DNA Structure
DNA has a double-helix structure. The...
DNA Structure
DNA has a double-helix structure. The...
The Replisome
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with the...
Genomic DNA in Eukaryotes
Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
Chromatin Packaging
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...


