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Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
Introduction to Virus01:28

Introduction to Virus

Viruses are unique biological entities that blur the boundary between living and non-living systems. Although they lack cellular structure and metabolic processes, they can exhibit characteristics of life when infecting a host. Their defining feature is a nucleic acid core, composed of either DNA or RNA, encapsulated within a protein coat called a capsid. This simple structure allows them to invade host cells and use their machinery for replication efficiently.Viral Structure and...
What are Viruses?00:50

What are Viruses?

Overview
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.
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...
Intracellular Movement of Viruses and Bacteria01:10

Intracellular Movement of Viruses and Bacteria

Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a virus that...

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Related Experiment Video

Updated: Jun 8, 2026

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
09:08

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus

Published on: July 27, 2021

[Envelope virus assembly and budding].

Takashi Irie1

  • 1Department of Virology, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima 734-8551, Japan. tirie@hiroshima-u.ac.jp

Uirusu
|September 21, 2010
PubMed
Summary

Sendai virus budding involves unique interactions with the ESCRT pathway component Alix/AIP1, mediated by the viral C protein. This protein also regulates viral RNA synthesis for efficient virus production.

Area of Science:

  • Virology
  • Molecular and Cell Biology

Context:

  • Enveloped viruses utilize matrix and Gag proteins for budding into virus-like particles (VLPs).
  • L-domain motifs (PPxY, P(T/S)AT, YP(x)(n)L) often mediate interactions with the host ESCRT pathway for viral budding.
  • ESCRT pathway involvement and L-domain motifs are uncharacterized in many enveloped viruses.

Purpose:

  • To investigate the mechanism of Sendai virus (SeV) budding and its reliance on the ESCRT pathway.
  • To identify the roles of SeV matrix (M) and accessory C proteins in viral assembly and budding.

Summary:

  • Sendai virus M protein interacts with the ESCRT component Alix/AIP1, but M-VLPs budding is not ESCRT-dependent.
  • The SeV C protein interacts with Alix/AIP1, recruiting it to the plasma membrane to promote M-VLPs budding.

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Simple and Robust in vivo and in vitro Approach for Studying Virus Assembly
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Simple and Robust in vivo and in vitro Approach for Studying Virus Assembly

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Modeling The Lifecycle Of Ebola Virus Under Biosafety Level 2 Conditions With Virus-like Particles Containing Tetracistronic Minigenomes
10:11

Modeling The Lifecycle Of Ebola Virus Under Biosafety Level 2 Conditions With Virus-like Particles Containing Tetracistronic Minigenomes

Published on: September 27, 2014

Related Experiment Videos

Last Updated: Jun 8, 2026

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
09:08

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus

Published on: July 27, 2021

Simple and Robust in vivo and in vitro Approach for Studying Virus Assembly
09:47

Simple and Robust in vivo and in vitro Approach for Studying Virus Assembly

Published on: March 1, 2012

Modeling The Lifecycle Of Ebola Virus Under Biosafety Level 2 Conditions With Virus-like Particles Containing Tetracistronic Minigenomes
10:11

Modeling The Lifecycle Of Ebola Virus Under Biosafety Level 2 Conditions With Virus-like Particles Containing Tetracistronic Minigenomes

Published on: September 27, 2014

  • SeV C protein also regulates viral genome and antigenome RNA synthesis for optimal infectious particle production.
  • Impact:

    • Reveals a unique budding mechanism for Sendai virus.
    • Identifies a novel role for the viral C protein in ESCRT recruitment and regulation of viral RNA synthesis.
    • Provides insights into efficient production of infectious viral particles.