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Related Concept Videos

Viral Recombination00:57

Viral Recombination

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Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
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SNAREs and Membrane Fusion01:43

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Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
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Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
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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...
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Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
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Related Experiment Video

Updated: Oct 6, 2025

Cell-cell Fusion of Genome Edited Cell Lines for Perturbation of Cellular Structure and Function
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Cell-cell Fusion of Genome Edited Cell Lines for Perturbation of Cellular Structure and Function

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Virus-cell and cell-cell fusion

L D Hernandez1, L R Hoffman, T G Wolfsberg

  • 1Department of Cell Biology, University of Virginia, Charlottesville 22908, USA.

Annual Review of Cell and Developmental Biology
|January 1, 1996
PubMed
Summary
This summary is machine-generated.

Viral fusion proteins undergo conformational changes to expose fusion peptides, initiating membrane fusion. Cell-cell fusion mechanisms are less understood, but ADAM proteins are potential candidates.

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Related Experiment Videos

Last Updated: Oct 6, 2025

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Method for Measurement of Viral Fusion Kinetics at the Single Particle Level
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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Background:

  • Viral membrane fusion proteins are crucial for infection and have distinct pH-dependent mechanisms.
  • Understanding viral fusion mechanisms provides insights into cellular fusion processes.

Purpose of the Study:

  • To review the mechanisms of viral membrane fusion proteins.
  • To discuss the potential role of ADAM proteins in cell-cell fusion.

Main Methods:

  • Literature review of viral fusion protein mechanisms.
  • Analysis of evidence for triggered conformational changes and fusion peptide exposure.
  • Identification of candidate cell-surface proteins involved in fusion.

Main Results:

  • Viral fusion proteins utilize triggered conformational changes to expose fusion peptides, facilitating bilayer interaction.
  • Low and neutral pH-dependent fusion mechanisms are increasingly understood.
  • ADAM family proteins are emerging as candidates for mediating cell-cell fusion.

Conclusions:

  • Viral fusion protein mechanisms provide a framework for understanding membrane fusion.
  • Further research into ADAM proteins is needed to confirm their role in cell-cell fusion.