TY - JOUR
T1 - The Desmosome is a Mesoscale Lipid Raft-Like Membrane Domain
AU - Lewis, Joshua D.
AU - Caldara, Amber L.
AU - Zimmer, Stephanie E.
AU - Seybold, Anna
AU - Strong, Nicole L.
AU - Stahley, Sara N.
AU - Frangakis, Achilleas S.
AU - Levental, Ilya
AU - Wahl, James K.
AU - Mattheyses, Alexa L.
AU - Sasaki, Takashi
AU - Nakabayashi, Kazuhiko
AU - Hata, Kenichiro
AU - Matsubara, Yoichi
AU - Ishida-Yamamoto, Akemi
AU - Amagai, Masayuki
AU - Kubo, Akiharu
AU - Kowalczyk, Andrew P.
N1 - Publisher Copyright:
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2018/8/27
Y1 - 2018/8/27
N2 - Desmogleins are cadherin family adhesion molecules essential for epidermal integrity. Previous studies have shown that desmogleins associate with lipid rafts, but the significance of this association was not clear. Here, we report that the desmoglein transmembrane domain (TMD) is the primary determinant of raft association. Further, we identify a novel mutation in the DSG1 TMD (G562R) that causes severe dermatitis, multiple allergies, and metabolic wasting (SAM) syndrome. Molecular modeling predicts that this G to R mutation shortens the DSG1 TMD, and experiments directly demonstrate that this mutation compromises both lipid raft association and desmosome incorporation. Finally, cryo-electron tomography (cryo-ET) indicates that the lipid bilayer within the desmosome is ~10% thicker than adjacent regions of the plasma membrane. These findings suggest that differences in bilayer thickness influence the organization of adhesion molecules within the epithelial plasma membrane, with cadherin TMDs recruited to the desmosome via establishment of a specialized mesoscale lipid raft-like membrane domain.
AB - Desmogleins are cadherin family adhesion molecules essential for epidermal integrity. Previous studies have shown that desmogleins associate with lipid rafts, but the significance of this association was not clear. Here, we report that the desmoglein transmembrane domain (TMD) is the primary determinant of raft association. Further, we identify a novel mutation in the DSG1 TMD (G562R) that causes severe dermatitis, multiple allergies, and metabolic wasting (SAM) syndrome. Molecular modeling predicts that this G to R mutation shortens the DSG1 TMD, and experiments directly demonstrate that this mutation compromises both lipid raft association and desmosome incorporation. Finally, cryo-electron tomography (cryo-ET) indicates that the lipid bilayer within the desmosome is ~10% thicker than adjacent regions of the plasma membrane. These findings suggest that differences in bilayer thickness influence the organization of adhesion molecules within the epithelial plasma membrane, with cadherin TMDs recruited to the desmosome via establishment of a specialized mesoscale lipid raft-like membrane domain.
UR - http://www.scopus.com/inward/record.url?scp=85095649113&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85095649113&partnerID=8YFLogxK
U2 - 10.1101/401455
DO - 10.1101/401455
M3 - Article
AN - SCOPUS:85095649113
JO - Mathematical Social Sciences
JF - Mathematical Social Sciences
SN - 0165-4896
ER -