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Structural Alterations of Mucins Are Associated with Losses in Functionality

  • Matthias Marczynski
  • , Kun Jiang
  • , Matthew Blakeley
  • , Vaibhav Srivastava
  • , Francisco Vilaplana
  • , Thomas Crouzier
  • , Oliver Lieleg
  • Technical University of Munich
  • AlbaNova University Center
  • Center for Autonomous Systems
  • Karolinska Institutet

Research output: Contribution to journalArticlepeer-review

80 Scopus citations

Abstract

Commercial mucin glycoproteins are routinely used as a model to investigate the broad range of important functions mucins fulfill in our bodies, including lubrication, protection against hostile germs, and the accommodation of a healthy microbiome. Moreover, purified mucins are increasingly selected as building blocks for multifunctional materials, i.e., as components of hydrogels or coatings. By performing a detailed side-by-side comparison of commercially available and lab-purified variants of porcine gastric mucins, we decipher key molecular motifs that are crucial for mucin functionality. As two main structural features, we identify the hydrophobic termini and the hydrophilic glycosylation pattern of the mucin glycoprotein; moreover, we describe how alterations in those structural motifs affect the different properties of mucins-on both microscopic and macroscopic levels. This study provides a detailed understanding of how distinct functionalities of gastric mucins are established, and it highlights the need for high-quality mucins-for both basic research and the development of mucin-based medical products.

Original languageEnglish
Pages (from-to)1600-1613
Number of pages14
JournalBiomacromolecules
Volume22
Issue number4
DOIs
StatePublished - 12 Apr 2021

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