TY - JOUR
T1 - Assembly of Model Membrane Nanodiscs for Native Mass Spectrometry
AU - Kostelic, Marius M.
AU - Zak, Ciara K.
AU - Jayasekera, Hiruni S.
AU - Marty, Michael T.
N1 - Funding Information:
The pMSP1D1 plasmid was a gift from Stephen Sligar (Addgene plasmid #20061). The authors thank Maria Reinhardt-Szyba, Kyle Fort, and Alexander Makarov at Thermo Fisher Scientific for their support on the UHMR Q-Exactive HF instrument. This work was funded by the National Science Foundation (CHE-1845230).
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/4/13
Y1 - 2021/4/13
N2 - Native mass spectrometry (MS) with nanodiscs is a promising technique for characterizing membrane protein and peptide interactions in lipid bilayers. However, prior studies have used nanodiscs made of only one or two lipids, which lack the complexity of a natural lipid bilayer. To better model specific biological membranes, we developed model mammalian, bacterial, and mitochondrial nanodiscs with up to four different phospholipids. Careful selection of lipids with similar masses that balance the fluidity and curvature enabled these complex nanodiscs to be assembled and resolved with native MS. We then applied this approach to characterize the specificity and incorporation of LL-37, a human antimicrobial peptide, in single-lipid nanodiscs versus model bacterial nanodiscs. Overall, development of these model membrane nanodiscs reveals new insights into the assembly of complex nanodiscs and provides a useful toolkit for studying membrane protein, peptide, and lipid interactions in model biological membranes.
AB - Native mass spectrometry (MS) with nanodiscs is a promising technique for characterizing membrane protein and peptide interactions in lipid bilayers. However, prior studies have used nanodiscs made of only one or two lipids, which lack the complexity of a natural lipid bilayer. To better model specific biological membranes, we developed model mammalian, bacterial, and mitochondrial nanodiscs with up to four different phospholipids. Careful selection of lipids with similar masses that balance the fluidity and curvature enabled these complex nanodiscs to be assembled and resolved with native MS. We then applied this approach to characterize the specificity and incorporation of LL-37, a human antimicrobial peptide, in single-lipid nanodiscs versus model bacterial nanodiscs. Overall, development of these model membrane nanodiscs reveals new insights into the assembly of complex nanodiscs and provides a useful toolkit for studying membrane protein, peptide, and lipid interactions in model biological membranes.
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U2 - 10.1021/acs.analchem.1c00735
DO - 10.1021/acs.analchem.1c00735
M3 - Article
AN - SCOPUS:85104910533
SN - 0003-2700
VL - 93
SP - 5972
EP - 5979
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 14
ER -