Intestinal Gel-Forming Mucins Polymerize by Disulfide-Mediated Dimerization of D3 Domains

• Published in: Journal of molecular biology Vol. 431; no. 19; pp. 3740 - 3752
• Main Authors: Javitt, Gabriel, Calvo, María Luisa Gómez, Albert, Lis, Reznik, Nava, Ilani, Tal, Diskin, Ron, Fass, Deborah
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 06.09.2019; Elsevier
• Subjects: colon; disulfide bonds; Golgi; mucin; quaternary structure; VWF; DTT; D1D2D3CysD1; D1D2D3; SDS-PAGE; disulfide bonds; quaternary structure; MUC2; MUC2D3; SEC-MALS; endoH; mucin; colon; Golgi
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1016/j.jmb.2019.07.018

The mucin 2 glycoprotein assembles into a complex hydrogel that protects intestinal epithelia and houses the gut microbiome. A major step in mucin 2 assembly is further multimerization of preformed mucin dimers, thought to produce a honeycomb-like arrangement upon hydrogel expansion. Important open questions are how multiple mucin 2 dimers become covalently linked to one another and how mucin 2 multimerization compares with analogous processes in related polymers such as respiratory tract mucins and the hemostasis protein von Willebrand factor. Here we report the x-ray crystal structure of the mucin 2 multimerization module, found to form a dimer linked by two intersubunit disulfide bonds. The dimer structure calls into question the current model for intestinal mucin assembly, which proposes disulfide-mediated trimerization of the same module. Key residues making interactions across the dimer interface are highly conserved in intestinal mucin orthologs, supporting the physiological relevance of the observed quaternary structure. With knowledge of the interface residues, it can be demonstrated that many of these amino acids are also present in other mucins and in von Willebrand factor, further indicating that the stable dimer arrangement reported herein is likely to be shared across this functionally broad protein family. The mucin 2 module structure thus reveals the manner by which both mucins and von Willebrand factor polymerize, drawing deep structural parallels between macromolecular assemblies critical to mucosal epithelia and the vasculature. [Display omitted] •Network formation by gel-forming mucins protects epithelia but is poorly understood•Intestinal mucin N-terminal module dimerizes rather than trimerizes•The mucin dimer forms through atypical protein-protein interaction sites•Gut mucins and a blood hemostasis factor share polymerization mechanisms