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Bjorkholm, Patrik
Alternative names
Publications (2 of 2) Show all publications
Hacke, M., Bjorkholm, P., Hellwig, A., Himmels, P., de Almodovar, C. R., Bruegger, B., . . . Ernst, A. M. (2015). Inhibition of Ebola virus glycoprotein-mediated cytotoxicity by targeting its transmembrane domain and cholesterol. Nature Communications, 6, Article ID 7688.
Open this publication in new window or tab >>Inhibition of Ebola virus glycoprotein-mediated cytotoxicity by targeting its transmembrane domain and cholesterol
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2015 (English)In: Nature Communications, ISSN 2041-1723, E-ISSN 2041-1723, Vol. 6, article id 7688Article in journal (Refereed) Published
Abstract [en]

The high pathogenicity of the Ebola virus reflects multiple concurrent processes on infection. Among other important determinants, Ebola fusogenic glycoprotein (GP) has been associated with the detachment of infected cells and eventually leads to vascular leakage and haemorrhagic fever. Here we report that the membrane-anchored GP is sufficient to induce the detachment of adherent cells. The results show that the detachment induced through either full-length GP(1,2) or the subunit GP(2) depends on cholesterol and the structure of the transmembrane domain. These data reveal a novel molecular mechanism in which GP regulates Ebola virus assembly and suggest that cholesterol-reducing agents could be useful as therapeutics to counteract GP-mediated cell detachment.

National Category
Biochemistry and Molecular Biology
Identifiers
urn:nbn:se:uu:diva-261317 (URN)10.1038/ncomms8688 (DOI)000358858100032 ()26158910 (PubMedID)
Available from: 2015-09-03 Created: 2015-09-01 Last updated: 2017-12-04Bibliographically approved
Björkholm, P., Harish, A., Hagström, E., Ernst, A. M. & Andersson, S. G. E. (2015). Mitochondrial genomes are retained by selective constraints on protein targeting. Proceedings of the National Academy of Sciences of the United States of America, 112(33), 10154-10161
Open this publication in new window or tab >>Mitochondrial genomes are retained by selective constraints on protein targeting
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2015 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 112, no 33, p. 10154-10161Article in journal (Refereed) Published
Abstract [en]

Mitochondria are energy-producing organelles in eukaryotic cells considered to be of bacterial origin. The mitochondrial genome has evolved under selection for minimization of gene content, yet it is not known why not all mitochondrial genes have been transferred to the nuclear genome. Here, we predict that hydrophobic membrane proteins encoded by the mitochondrial genomes would be recognized by the signal recognition particle and targeted to the endoplasmic reticulum if they were nuclear-encoded and translated in the cytoplasm. Expression of the mitochondrially encoded proteins Cytochrome oxidase subunit 1, Apocytochrome b, and ATP synthase subunit 6 in the cytoplasm of HeLa cells confirms export to the endoplasmic reticulum. To examine the extent to which the mitochondrial proteome is driven by selective constraints within the eukaryotic cell, we investigated the occurrence of mitochondrial protein domains in bacteria and eukaryotes. The accessory protein domains of the oxidative phosphorylation system are unique to mitochondria, indicating the evolution of new protein folds. Most of the identified domains in the accessory proteins of the ribosome are also found in eukaryotic proteins of other functions and locations. Overall, one-third of the protein domains identified in mitochondrial proteins are only rarely found in bacteria. We conclude that the mitochondrial genome has been maintained to ensure the correct localization of highly hydrophobic membrane proteins. Taken together, the results suggest that selective constraints on the eukaryotic cell have played a major role in modulating the evolution of the mitochondrial genome and proteome.

Keywords
mitochondria, protein domain, evolution, endoplasmatic reticulum, signal recognition particle
National Category
Biological Sciences
Identifiers
urn:nbn:se:uu:diva-262430 (URN)10.1073/pnas.1421372112 (DOI)000359738300037 ()26195779 (PubMedID)
Funder
Swedish Research Council, 621-2011-4669Knut and Alice Wallenberg Foundation, 2011.148
Note

P.B. och A.H delar förstaförfattarskapet.

Available from: 2015-09-17 Created: 2015-09-15 Last updated: 2017-12-04Bibliographically approved
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