SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Lässer Cecilia 1981)
 

Sökning: WFRF:(Lässer Cecilia 1981) > Detailed Analysis o...

Detailed Analysis of Protein Topology of Extracellular Vesicles–Evidence of Unconventional Membrane Protein Orientation

Cvjetkovic, Aleksander (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Jang, Su Chul, 1984 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Konečná, Barbora (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
visa fler...
Höög, Johanna L, 1979 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre,Institutionen för kemi och molekylärbiologi,Department of Chemistry and Molecular Biology
Sihlbom, Carina, 1973 (författare)
Gothenburg University,Göteborgs universitet,Core Facilities, Proteomics,Core Facilities, Proteomics
Lässer, Cecilia, 1981 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
Lötvall, Jan, 1956 (författare)
Gothenburg University,Göteborgs universitet,Krefting Research Centre
visa färre...
 (creator_code:org_t)
2016-11-08
2016
Engelska.
Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 6
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Extracellular vesicles (EVs) are important mediators of intercellular communication that change the recipient cell by shuttling lipids, RNA, or protein cargo between cells. Here, we investigate the topology of the protein cargo found in EVs, as this topology can fundamentally influence the biological effects of EVs. A multiple proteomics approach, combining proteinase treatment and biotin tagging, shows that many proteins of cytosolic origin are localized on the surface of EVs. A detailed analysis of the EV proteome at the peptide level revealed that a number of EV membrane proteins are present in a topologically reversed orientation compared to what is annotated. Two examples of such proteins, SCAMP3 and STX4, were confirmed to have a reversed topology. This reversed typology was determined using flow cytometry and fluorescent microscopy with antibodies directed toward their cytoplasmic epitopes. These results describe a novel workflow to define the EV proteome and the orientation of each protein, including membrane protein topology. These data are fundamentally important to understanding the EV proteome and required to fully explain EV biogenesis as well as biological function in recipient cells.

Ämnesord

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)

Nyckelord

exosome
proteomics
electron microscopy
vesicle

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy