関連する実験動画
Updated: Jul 12, 2026

13:42
RNA Secondary Structure Prediction Using High-throughput SHAPE
Published on: May 31, 2013
核酸の完全な,配列依存の折り畳み風景の直接測定
Michael T Woodside1, Peter C Anthony, William M Behnke-Parks
1National Institute for Nanotechnology, National Research Council of Canada, Edmonton AB, Canada, T6G 2M9.
まとめ
研究者は,単一分子力クランプ実験を使用して,DNAのヘアピン折りたたみエネルギー風景をマッピングしました. 彼らはDNA配列と不一致を変化させることで,折り畳み障壁と中間物質を正確に制御しました.
科学分野:
- バイオフィジックス 生物物理学
- 分子生物学は分子生物学である.
- 遺伝学 遺伝学とは
背景:
- 核酸ヘアピンとは,マクロ分子折り畳みを研究するためのモデルシステムです.
- 彼らの自由エネルギー風景は,その配列を変更することによって操作することができます.
- 折り畳みダイナミクスを理解することは,分子生物学にとって極めて重要です.
研究 の 目的:
- リバーシブルなDNAヘアピン折りたたみのための完全なエネルギー景観を取得するために.
- 配列変更が負荷下での折り畳みダイナミクスにどのように影響するか調査する.
- 折り畳み障壁と中間物質を制御するには,特定の配列要素を使用します.
主な方法:
- 制御された機械的負荷を適用するために単分子力クランプの実験を活用しました.
- 折り畳みイベントを捉えるために高解像度の単分子軌道を採用しました.
- 軌道データからエネルギー景観を再構築するために,デコンボレーション技術を適用した.
主要な成果:
- DNAヘアピン折り畳みのための完全なエネルギー風景のマッピングに成功しました.
- G:C塩基ペアの数と位置がエネルギーバリアの高さと位置を調整することを示した.
- シングル・ヌクレオチドの不一致が,折りたたみの中間物質の存在と位置を制御することを示した.
結論:
- この研究は,DNAのヘアピン折りたたみエネルギー景観の高解像度ビューを提供します.
- 配列操作は,折り畳み経路とエネルギーの正確な制御を提供します.
- 発見は,核酸のダイナミクスと折り畳み原理の理解を進める.
関連する概念動画
Sanger Sequencing
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
RNA-seq
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Ribosome Profiling
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...
Maxam-Gilbert Sequencing
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...
Nuclear Overhauser Enhancement (NOE)
Irradiation of a spin-active nucleus causes an increase or decrease in the signal intensity of neighboring nuclei that are not necessarily chemically bonded or involved in J-coupling. This phenomenon, called the nuclear Overhauser enhancement (NOE), results from through-space interactions between the nuclear spins. The NOE effect decreases with increasing internuclear distance and is generally not observed beyond 4 angstroms. In NOE, dipole-dipole interactions between neighboring spin-active...
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...

