Number of the records: 1  

The use of styrene-maleic acid copolymer (SMA) for studies on T cell membrane rafts

  1. 1.
    0501169 - ÚMG 2020 RIV NL eng J - Journal Article
    Angelisová, Pavla - Ballek, Ondřej - Sýkora, Jan - Benada, Oldřich - Čajka, Tomáš - Pokorná, Jana - Pinkas, Dominik - Hořejší, Václav
    The use of styrene-maleic acid copolymer (SMA) for studies on T cell membrane rafts.
    Biochimica Et Biophysica Acta-Biomembranes. Roč. 1861, č. 1 (2019), s. 130-141. ISSN 0005-2736. E-ISSN 1879-2642
    R&D Projects: GA ČR(CZ) GA17-05903S; GA MŠMT(CZ) LO1509; GA MŠMT(CZ) LM2015062; GA ČR(CZ) GBP302/12/G101; GA MŠMT(CZ) EF16_013/0001775
    Institutional support: RVO:68378050 ; RVO:67985823 ; RVO:61388971 ; RVO:61388955
    Keywords : Membrane rafts * sma * GPI-anchored proteins * T lymphocytes * Src family kinases * Membrane proteins
    OECD category: Biochemistry and molecular biology; Physical chemistry (UFCH-W); Microbiology (MBU-M); Analytical chemistry (FGU-C)
    Impact factor: 3.411, year: 2019
    Method of publishing: Open access
    https://doi.org/10.1016/j.bbamem.2018.08.006

    An emerging alternative to the use of detergents in biochemical studies on membrane proteins is apparently the use styrene-maleic acid (SMA) amphipathic copolymers. These cut the membrane into nanodiscs (SMA-lipid particles, SMALPs), which contain membrane proteins possibly surrounded by their native lipid environment. We examined this approach for studies on several types of T cell membrane proteins, previously defined as raft or non-raft associated, to see whether the properties of the raft derived SMALPs differ from non-raft SMALPs. Our results indicate that two types of raft proteins, GPI-anchored proteins and two Src family kinases, are markedly present in membrane fragments much larger (> 250 nm) than those containing non-raft proteins (< 20 nm). Lipid probes sensitive to membrane fluidity (membrane order) indicate that the lipid environment in the large SMALPs is less fluid (more ordered) than in the small ones which may indicate the presence of a more ordered lipid L-o phase which is characteristic of membrane rafts. Also the lipid composition of the small vs. large SMALPs is markedly different the large ones are enriched in cholesterol and lipids containing saturated fatty acids. In addition, we confirm that T cell membrane proteins present in SMALPs can be readily immunoisolated. Our results support the use of SMA as a potentially better (less artifact prone) alternative to detergents for studies on membrane proteins and their complexes, including membrane rafts.
    Permanent Link: http://hdl.handle.net/11104/0293384

     
    FileDownloadSizeCommentaryVersionAccess
    0501169.pdf92.8 MBPublisher’s postprintrequire
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.