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関連する概念動画

Inhibitors of Virion Maturation and Assembly01:19

Inhibitors of Virion Maturation and Assembly

As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...
Viral Structure00:56

Viral Structure

Viruses are extraordinarily diverse in shape and size, but they all have several structural features in common. All viruses have a core that contains a DNA- or RNA-based genome. The core is surrounded by a protective coat of proteins called the capsid. The capsid is composed of subunits called capsomeres. The capsid and genome-containing core are together known as the nucleocapsid.
Protein Complex Assembly02:41

Protein Complex Assembly

Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Protein Complex Assembly02:41

Protein Complex Assembly

Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Leaky Scanning02:28

Leaky Scanning

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 stands for...
Intralumenal Vesicles and Multivesicular Bodies01:38

Intralumenal Vesicles and Multivesicular Bodies

Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...

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関連する実験動画

Updated: Jul 6, 2026

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
12:20

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses

Published on: December 29, 2015

フラビウイルス前駆体である膜包膜タンパク質複合体:構造と成熟.

Long Li1, Shee-Mei Lok, I-Mei Yu

  • 1Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.

Science (New York, N.Y.)
|March 29, 2008
PubMed
まとめ

フラビウイルスは,前駆性膜タンパク質 (prM) の割れ方によって成熟し,惰性ウイルスを感染性粒子に変換します. この研究は,デング熱ウイルスのprM-Eヘテロダイマー構造を明らかにし,成熟と宿主細胞融合阻害を説明しています.

科学分野:

  • ウイルス学 ウイルス学 ウイルス学
  • 構造生物学 構造生物学とは
  • 分子生物学は分子生物学である.

背景:

  • ウイルスの成熟は,タンパク質の処理を含む感染性にとって極めて重要です.
  • フラビウイルスの成熟は,前駆体膜タンパク質 (prM) のタンパク質分解による分裂に依存しています.

研究 の 目的:

  • デング熱ウイルスの高解像度の結晶構造を決定する prM-E ヘテロダイマー.
  • フラビウイルス成熟と宿主細胞融合阻害の構造的基礎を解明する.

主な方法:

  • 2.2アングストームの解像度のX線結晶学.
  • 再結合タンパク質の発現と浄化.
  • クリオ電子顕微鏡密度フィッティング.

主要な成果:

  • デング熱ウイルスのprM-Eヘテロダイマーの結晶構造が決定されました.
  • prペプチドは,Eグリコタンパク質の融合ループをシールドし,膜融合を防ぐ.
  • 構造は,中性pHの未成熟ウイルスの冷凍-EMデータと一致しています.

結論:

さらに関連する動画

Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses
08:10

Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses

Published on: January 15, 2020

Averaging of Viral Envelope Glycoprotein Spikes from Electron Cryotomography Reconstructions using Jsubtomo
08:29

Averaging of Viral Envelope Glycoprotein Spikes from Electron Cryotomography Reconstructions using Jsubtomo

Published on: October 21, 2014

関連する実験動画

Last Updated: Jul 6, 2026

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses
12:20

Bacterial Artificial Chromosomes: A Functional Genomics Tool for the Study of Positive-strand RNA Viruses

Published on: December 29, 2015

Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses
08:10

Production of High-Titer Infectious Influenza Pseudotyped Particles with Envelope Glycoproteins from Highly Pathogenic H5N1 and Avian H7N9 Viruses

Published on: January 15, 2020

Averaging of Viral Envelope Glycoprotein Spikes from Electron Cryotomography Reconstructions using Jsubtomo
08:29

Averaging of Viral Envelope Glycoprotein Spikes from Electron Cryotomography Reconstructions using Jsubtomo

Published on: October 21, 2014

  • prM-E構造は,フラビウイルス成熟の分子理解を提供します.
  • これは,prペプチドが融合を阻害するメカニズムを明らかにします.
  • この構造的洞察は,ウイルスの成熟過程におけるpHに依存する形状の変化を理解するのに役立ちます.