X線結晶学では,mRNAキャピング酵素によるグアナイル移転中に大きな形状の変化が明らかにされています
K Håkansson1, A J Doherty, S Shuman
1Laboratory of Molecular Biophysics, University of Oxford, United Kingdom.
Cell
|May 16, 1997
まとめ
私たちはmRNAキャピング酵素の結晶構造を解明し,触媒に不可欠な構成変化を明らかにしました. これは,GTP結合とマンガンイオン調整を含む酵素の触媒機構の直接的な証拠を提供します.
科学分野:
- バイオケミストリー バイオケミストリー
- 構造生物学 構造生物学とは
- 酵素学 酵素学とは
背景:
- mRNAキャピングは,真核生物の遺伝子発現において重要なプロセスである.
- mRNAキャピング酵素の仕組みを理解することは,分子生物学にとって不可欠です.
研究 の 目的:
- mRNAキャピング酵素機能の構造的基礎を解明する.
- 酵素の触媒サイクルに関する機械的洞察を提供するため.
主な方法:
- 2.5A解像度で酵素構造を決定するために,X線結晶学を用いた.
- この研究では,開いた状態と閉じた状態を含む,異なる酵素構成を分析した.
- 触媒活性と中間形成は,結晶状態で調査されました.
主要な成果:
- mRNAキャピング酵素は,狭い裂け目を持つ2ドメイン構造を持っています.
- 2つの異なる酵素構成が観察されました:開いたものと閉じられたもので,どちらもGTPと結合しています.
- 閉ざされた形状は,マンガンイオン結合と触媒を容易にし,ガニリ化中間物質を形成します.
結論:
- 酵素は,触媒作用中に重要な形状変化を経験します.
- この形状の柔軟性は,mRNAキャピングメカニズムの鍵です.
- 結晶構造は,提案された触媒機構の直接的な証拠を提供します.
さらに関連する動画
11:27X-Ray Crystallography to Study the Oligomeric State Transition of the Thermotoga maritima M42 Aminopeptidase TmPep1050
Published on: May 13, 2020
3.4K
10:45Crystallization and Structural Determination of an Enzyme:Substrate Complex by Serial Crystallography in a Versatile Microfluidic Chip
Published on: March 20, 2021
9.9K
関連する概念動画
pre-mRNA Processing
49.0K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
49.0K
Improving Translational Accuracy
11.6K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.6K
Termination of Translation
19.7K
The large ribosomal subunit has several important structures essential to translation. These include the peptidyl transferase center (PTC) - which is the site where the peptide bond is formed - and a large, internal, water-filled tube through which the nascent polypeptide moves. This latter structure is called the Peptide Exit Tunnel, and it begins at the PTC and spans the body of the large ribosomal subunit. During translation, as the nascent polypeptide chain is synthesized, it passes through...
19.7K
Leaky Scanning
4.5K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA. Marilyn Kozak discovered that the sequence RCCAUGG (where R...
4.5K
Directing Proteins to the Rough Endoplasmic Reticulum
12.1K
The organelle-specific signaling sequences direct proteins synthesized in the cytosol to their final destination like ER, mitochondria, peroxisomes, etc. Some of the proteins directed to ER are then trafficked via vesicles to other organelles within the cell or the extracellular environment through the Golgi complex. For example, the rough ER synthesizes soluble proteins for transportation to the lysosomes or secretion out of the cell. It can also synthesize transmembrane proteins that can...
12.1K
Pre-mRNA Processing: Modification of pre-mRNA Ends
14.2K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
14.2K
