Decellularized extracellular matrix (ECM) biomaterials derived from native tissues and organs are widely used for tissue engineering and wound repair. To boost their regenerative potential, ECM biomaterials can be functionalized via the immobilization of bioactive molecules. To enable ECM functionalization in a chemoselective manner, we have recently reported an effective approach for labeling native organ ECM with the click chemistry-reactive azide ligand via physiologic post-translational glycosylation. Here, using the rat lung as a model, we provide a detailed protocol for and metabolic azide labeling of the native organ ECM using N-Azidoacetylgalactosamine-tetraacylated (AcGalNAz), together with procedures for decellularization and labeling characterization. Our approach enables specific and robust ECM labeling within three days or within one day during organ culture. The resulting ECM labeling remains stable following decellularization. With our approach, ECM biomaterials can be functionalized with desired alkyne-modified biomolecules, such as growth factors and glycosaminoglycans, for tissue engineering and regenerative applications.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952949PMC
http://dx.doi.org/10.21769/BioProtoc.3922DOI Listing

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