[HTML][HTML] The Dystrophin Complex: structure, function and implications for therapy

Q Gao, EM McNally - Comprehensive physiology, 2015 - ncbi.nlm.nih.gov
The dystrophin complex stabilizes the plasma membrane of striated muscle cells. Loss of
function mutations in the genes encoding dystrophin, or the associated proteins, triggers …

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane

T Yoshida-Moriguchi, KP Campbell - Glycobiology, 2015 - academic.oup.com
Associations between cells and the basement membrane are critical for a variety of
biological events including cell proliferation, cell migration, cell differentiation and the …

Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy

M Kanagawa, K Kobayashi, M Tajiri, H Manya, A Kuga… - Cell reports, 2016 - cell.com
Glycosylation is an essential post-translational modification that underlies many biological
processes and diseases. α-dystroglycan (α-DG) is a receptor for matrix and synaptic proteins …

SGK196 Is a Glycosylation-Specific O-Mannose Kinase Required for Dystroglycan Function

T Yoshida-Moriguchi, T Willer, ME Anderson, D Venzke… - Science, 2013 - science.org
Phosphorylated O-mannosyl trisaccharide [N-acetylgalactosamine–β3-N-acetylglucosamine–
β4-(phosphate-6-) mannose] is required for dystroglycan to bind laminin-G domain …

Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins

MB Vester-Christensen, A Halim… - Proceedings of the …, 2013 - National Acad Sciences
The metazoan O-mannose (O-Man) glycoproteome is largely unknown. It has been shown
that up to 30% of brain O-glycans are of the O-Man type, but essentially only alpha …

Recent advancements in understanding mammalian O-mannosylation

MO Sheikh, SM Halmo, L Wells - Glycobiology, 2017 - academic.oup.com
The post-translational glycosylation of select proteins by O-linked mannose (O-mannose or
O-man) is a conserved modification from yeast to humans and has been shown to be …

Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly

S Vuillaumier-Barrot, C Bouchet-Séraphin… - The American Journal of …, 2012 - cell.com
Cobblestone lissencephaly is a peculiar brain malformation with characteristic radiological
anomalies. It is defined as cortical dysplasia that results when neuroglial overmigration into …

[HTML][HTML] Deep mutational scanning reveals functional constraints and antibody-escape potential of Lassa virus glycoprotein complex

CR Carr, KHD Crawford, M Murphy, JG Galloway… - Immunity, 2024 - cell.com
Lassa virus is estimated to cause thousands of human deaths per year, primarily due to
spillovers from its natural host, Mastomys rodents. Efforts to create vaccines and antibody …

TRAPPopathies: an emerging set of disorders linked to variations in the genes encoding transport protein particle (TRAPP)‐associated proteins

M Sacher, N Shahrzad, H Kamel, MP Milev - Traffic, 2019 - Wiley Online Library
The movement of proteins between cellular compartments requires the orchestrated actions
of many factors including Rab family GTPases, Soluble NSF Attachment protein REceptors …

Advances in mass spectrometry driven O-glycoproteomics

SB Levery, C Steentoft, A Halim, Y Narimatsu… - … Et Biophysica Acta (BBA …, 2015 - Elsevier
Background Global analyses of proteins and their modifications by mass spectrometry are
essential tools in cell biology and biomedical research. Analyses of glycoproteins represent …