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Neutron reflectometry and NMR spectroscopy of full-length Bcl-2 protein reveal its membrane localization and conformation

Ul Mushtaq, Ameeq (author)
Umeå universitet,Umeå University,Kemiska institutionen
Ådén, Jörgen, 1980- (author)
Umeå universitet,Umeå University,Kemiska institutionen
Clifton, L. A. (author)
ISIS Neutron and Muon Source
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Wacklin-Knecht, Hanna (author)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,European Spallation Source ERIC, Denmark
Campana, M. (author)
ISIS Neutron and Muon Source
Dingeldein, Artur P. G. (author)
Umeå universitet,Umeå University,Kemiska institutionen
Persson, Cecilia, 1974 (author)
University of Gothenburg,Gothenburg University,Göteborgs universitet,Svenskt NMR-centrum vid Göteborgs universitet,Swedish NMR Centre at Göteborg University
Sparrman, Tobias (author)
Umeå universitet,Umeå University,Kemiska institutionen
Grobner, G. (author)
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 (creator_code:org_t)
2021-04-27
2021
English.
In: Communications Biology. - : Springer Science and Business Media LLC. - 2399-3642. ; 4:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • B-cell lymphoma 2 (Bcl-2) proteins are the main regulators of mitochondrial apoptosis. Anti-apoptotic Bcl-2 proteins possess a hydrophobic tail-anchor enabling them to translocate to their target membrane and to shift into an active conformation where they inhibit pro-apoptotic Bcl-2 proteins to ensure cell survival. To address the unknown molecular basis of their cell-protecting functionality, we used intact human Bcl-2 protein natively residing at the mitochondrial outer membrane and applied neutron reflectometry and NMR spectroscopy. Here we show that the active full-length protein is entirely buried into its target membrane except for the regulatory flexible loop domain (FLD), which stretches into the aqueous exterior. The membrane location of Bcl-2 and its conformational state seems to be important for its cell-protecting activity, often infamously upregulated in cancers. Most likely, this situation enables the Bcl-2 protein to sequester pro-apoptotic Bcl-2 proteins at the membrane level while sensing cytosolic regulative signals via its FLD region. Through neutron reflectometry and NMR spectroscopy studies, Mushtaq et al study the full-length Bcl-2 protein reconstituted in lipid bilayers. They find that, in contrast to previously studied truncated, soluble protein versions, intact Bcl-2 is mainly embedded in the membrane with its regulatory loop highly flexible.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

lipid-membranes
family
bax
apoptosis
mitochondria
dynamics
xl
insertion
bcl-x(l)
software
Life Sciences & Biomedicine - Other Topics
Science & Technology - Other
Topics

Publication and Content Type

ref (subject category)
art (subject category)

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