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.

Approximately 10% of all hospital patients contract infections from temporary clinical implants such as urinal and vascular catheters or tracheal tubes. The ensuing complications reach from patient inconvenience and tissue inflammation to severe, life threatening complications such as pneumonia or bacteremia. All these device‐associated nosocomial infections have the same origin: biofouling, i.e., the unwanted deposition of proteins, bacteria, and cells onto the device. To date, most strategies to overcome these problems are device specific, which results in high development efforts and costs. Here, it is demonstrated how one and the same coupling mechanism can be used to create a covalent antifouling coating employing mucin glycoproteins on multiple materials: with this method, a stable mucin layer can be generated on a broad range of polymer materials which are frequently used in medical engineering. It is shown that the mucin coating exhibits excellent stability against mechanical, thermal, and chemical challenges and reduces protein adsorption as well as prokaryotic and eukaryotic cell adhesion. Thus, the coating mechanism described here introduces a promising strategy to overcome biofouling issues on a broad range of medical devices.

Charged, mucoadhesive molecules can penetrate mucin-based hydrogels such as native mucus with similar efficiency as inert, non-mucoadhesive molecules.

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