Related Experiment Video
Updated: Apr 27, 2026

07:30
Cell-cell Fusion of Genome Edited Cell Lines for Perturbation of Cellular Structure and Function
Published on: December 7, 2019
8.6K
Virus and cell fusion mechanisms
1Department of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel;
Annual Review of Cell and Developmental Biology
|July 9, 2014
Summary
Membrane fusion involves protein insertions and lipid reorganization. Four classes of viral and cellular fusion proteins (fusogens) are identified, each with distinct structures and mechanisms for membrane destabilization and fusion.
Area of Science:
- Biochemistry
- Cell Biology
- Virology
Background:
- Membrane fusion is crucial for viral entry and cellular processes.
- Fusogenic proteins destabilize membranes via lipid reorganization and protein restructuring.
- Four classes of viral and cellular fusion proteins are known.
Purpose of the Study:
- To review and classify known membrane fusion proteins.
- To elucidate the mechanisms of viral and cellular fusion.
- To highlight the diversity of fusogenic proteins and their structures.
Main Methods:
- Literature review of membrane fusion mechanisms.
- Classification of fusion proteins based on structure and function.
- Analysis of protein refolding and membrane interaction.
Main Results:
- Class I fusogens: α-helix-rich trimers inserting fusion peptides.
- Class II fusogens: β-sheet-rich dimers inserting fusion loops.
- Class III fusogens: α/β trimers dissociating and oligomerizing.
- Class IV fusogens: Small proteins with fusion loops mediating cell-cell fusion.
- Syncytins (Class I) and EFF-1/AFF-1 (Class II) are examples of cell-cell fusogens.
Conclusions:
- Distinct classes of fusogens utilize diverse structural strategies for membrane fusion.
- Understanding these mechanisms is key to deciphering viral entry and cell-cell fusion.
- Further research is needed to identify fusogens for many cell fusion events.
Related Concept Videos
Viral Recombination
22.2K
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.
22.2K
SNAREs and Membrane Fusion
10.3K
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.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
10.3K
Fusion of Secretory Vesicles with the Plasma Membrane
15.9K
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.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
15.9K
Intracellular Movement of Viruses and Bacteria
3.0K
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...
3.0K
Introduction to Virus
2.9K
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...
2.9K
Retroviruses
11.9K
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
11.9K

