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Related Concept Videos

Hepatitis01:25

Hepatitis

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Hepatitis is an inflammatory condition of the liver most commonly caused by hepatotropic viruses (A–E), though non-infectious causes such as alcohol and drugs also exist.Hepatitis AHepatitis A virus (HAV) is a non-enveloped RNA virus of the Picornaviridae family. It is primarily transmitted via the fecal-oral route, typically through ingestion of contaminated food or water. After ingestion, HAV enters the bloodstream through the oropharynx or intestinal epithelium and reaches the liver.
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Directing Proteins to the Rough Endoplasmic Reticulum01:34

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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...
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Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
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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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RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
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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...
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Related Experiment Video

Updated: Apr 4, 2026

Two Methods of Heterokaryon Formation to Discover HCV Restriction Factors
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Two Methods of Heterokaryon Formation to Discover HCV Restriction Factors

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SRFBP1, an Additional Player in HCV Entry.

Lucie Fénéant1, Laurence Cocquerel1

  • 1Université Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 8204 - CIIL -Centre d'Infection et d'Immunité de Lille, F-59000 Lille, France.

Trends in Microbiology
|August 31, 2015
PubMed
Summary

Serum response factor binding protein 1 (SRFBP1) interacts with CD81 during hepatitis C virus (HCV) infection. This interaction is crucial for the post-fusion viral entry process, highlighting a new target for HCV therapies.

Keywords:
Hepatitis C VirusSRFBP1entry factorprotein-protein interactionsproteomicsthe tetraspanin CD81

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Area of Science:

  • Virology
  • Molecular Cell Biology
  • Immunology

Background:

  • Tetraspanin CD81 is vital for hepatitis C virus (HCV) entry into host cells.
  • Protein interactions involving CD81 regulate viral pathogenesis.
  • Understanding CD81's partners is key to developing antiviral strategies.

Purpose of the Study:

  • To identify novel proteins interacting with CD81 during HCV infection.
  • To elucidate the role of these interactions in the viral post-fusion entry stage.

Main Methods:

  • Proteomic analysis was employed to identify CD81-interacting proteins.
  • Co-immunoprecipitation assays confirmed protein-protein interactions.
  • HCV infection models were used to study the functional relevance of identified proteins.

Main Results:

  • Serum response factor binding protein 1 (SRFBP1) was identified as a novel CD81-interacting protein.
  • SRFBP1 was found to associate with CD81 during the post-fusion phase of HCV entry.
  • This interaction plays a role in facilitating viral entry after membrane fusion.

Conclusions:

  • SRFBP1 is a key mediator in the CD81-dependent post-fusion entry of HCV.
  • Targeting the SRFBP1-CD81 interaction may offer a new therapeutic strategy against HCV infection.