Assembling and decorating hyaluronan hydrogels with twin protein superglues to mimic cell-cell interactions. (October 2018)

• Record Type: Journal Article
• Authors: Wieduwild, Robert; Howarth, Mark
• Is Part Of: Biomaterials. Volume 180(2018)
• Page Start: 253
• Page End: 264
• Publication Date: 2018-10
• Subjects: Protein engineering -- Bioconjugation -- Polysaccharide -- Hyaluronic acid -- Glycobiology -- Bioengineering; Biomedical materials -- Periodicals; Biocompatible Materials -- Periodicals; Biomatériaux -- Périodiques; 610.28
• DOI: 10.1016/j.biomaterials.2018.07.020
• Languages: English
• ISSNs: 0142-9612

Abstract

Abstract: Simple polymeric scaffolds have yielded dramatic effects on cell behavior. For more sophisticated phenotypes, precise and efficient chemistries are desired to incorporate proteins into these scaffolds. Here we derivatize hyaluronan with an elastin-like polypeptide containing telechelic SpyTags (HA-SpyTag). Our second network component, the TriCatcher protein, had two SpyCatchers and a terminal SnoopCatcher. Mixing HA-SpyTag with TriCatcher led to rapid hydrogel formation, via spontaneous amidation. SnoopCatcher allowed modular network decoration with SnoopTagJr-linked adhesion molecules, through orthogonal transamidation. This programmed scaffold enables the testing of how individual matrix-anchored protein interactions affect cell behavior. Epithelial cell adhesion molecule (EpCAM) regulates cell behavior and migration, with important effects in cancer. EpCAM-anchoring to the hydrogel induced disassembly of non-malignant mammary spheres in 3D culture. Integrating signaling proteins into biomaterials via efficient biocompatible chemistry should reveal key cues to control cell behavior. Graphical abstract: Image 1