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Lipid exchange of apolipoprotein A-I amyloidogenic variants in reconstituted high-density lipoprotein with artificial membranes

Correa, Yubexi (author)
Malmö universitet,Malmö University,Biofilms Research Center for Biointerfaces,Institutionen för biomedicinsk vetenskap (BMV)
Ravel, Mathilde (author)
Malmö universitet,Malmö University,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces
Imbert, Marie (author)
Malmö universitet,Malmö University,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces
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Waldie, Sarah (author)
Malmö universitet,Malmö University,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces
Clifton, Luke (author)
ISIS Neutron and Muon Source,Harwell Sci & Innovat Campus, Sci & Technol Facil Council, Rutherford Appleton Lab, ISIS Pulsed Neutron & Muon Source, Didcot, England.
Terry, Ann (author)
Lund University,Lunds universitet,MAX IV-laboratoriet,MAX IV Laboratory,Lund Univ, MAX Lab 4, CoSAXS Beamline, Lund, Sweden.
Roosen-Runge, Felix (author)
Malmö universitet,Malmö University,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces
Lagerstedt, Jens O. (author)
Lund University,Lunds universitet,Diabetes - öcellsexocytos,Forskargrupper vid Lunds universitet,Diabetes - Islet Cell Exocytosis,Lund University Research Groups,Novo Nordisk A/S,Lund Univ, Diabet Ctr, Dept Clin Sci Malmö, Islet Cell Exocytosis, Malmö, Sweden.;Novo Nordisk, Rare Endocrine Disorders, Res & Early Dev, Copenhagen, Denmark.
Moir, Michael (author)
Australian Nuclear Science and Technology Organisation,Australian Nucl Sci & Technol Org ANSTO, Natl Deuterat Facil, Lucas Heights, NSW, Australia.
Darwish, Tamim (author)
University of Canberra,Australian Nuclear Science and Technology Organisation,Australian Nucl Sci & Technol Org ANSTO, Natl Deuterat Facil, Lucas Heights, NSW, Australia.;Univ Canberra, Fac Sci & Technol, Canberra, ACT, Australia.
Cárdenas, Marité (author)
Malmö universitet,Malmö University,Basque Foundation for Science,University of the Basque Country,CSIC Spanish National Research Council,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces,Basque Fdn Sci, Ikerbasque, Bilbao, Spain.;Univ Basque Country, Biofis Inst, Leioa, Spain.
Del Giudice, Rita (author)
Malmö universitet,Malmö University,Biofilms Research Center for Biointerfaces,Institutionen för biomedicinsk vetenskap (BMV)
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 (creator_code:org_t)
John Wiley & Sons, 2024
2024
English 16 s.
In: Protein Science. - : John Wiley & Sons. - 0961-8368 .- 1469-896X. ; 33:5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • High-density lipoproteins (HDLs) are responsible for removing cholesterol from arterial walls, through a process known as reverse cholesterol transport. The main protein in HDL, apolipoprotein A-I (ApoA-I), is essential to this process, and changes in its sequence significantly alter HDL structure and functions. ApoA-I amyloidogenic variants, associated with a particular hereditary degenerative disease, are particularly effective at facilitating cholesterol removal, thus protecting carriers from cardiovascular disease. Thus, it is conceivable that reconstituted HDL (rHDL) formulations containing ApoA-I proteins with functional/structural features similar to those of amyloidogenic variants hold potential as a promising therapeutic approach. Here we explored the effect of protein cargo and lipid composition on the function of rHDL containing one of the ApoA-I amyloidogenic variants G26R or L174S by Fourier transformed infrared spectroscopy and neutron reflectometry. Moreover, small-angle x-ray scattering uncovered the structural and functional differences between rHDL particles, which could help to comprehend higher cholesterol efflux activity and apparent lower phospholipid (PL) affinity. Our findings indicate distinct trends in lipid exchange (removal vs. deposition) capacities of various rHDL particles, with the rHDL containing the ApoA-I amyloidogenic variants showing a markedly lower ability to remove lipids from artificial membranes compared to the rHDL containing the native protein. This effect strongly depends on the level of PL unsaturation and on the particles' ultrastructure. The study highlights the importance of the protein cargo, along with lipid composition, in shaping rHDL structure, contributing to our understanding of lipid–protein interactions and their behavior.

Subject headings

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

Keyword

amyloidogenic variants
apolipoprotein A-I
high-density lipoprotein
reconstituted HDL
amyloidogenic variants

Publication and Content Type

art (subject category)
ref (subject category)

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