An experimental toolbox for characterization of mammalian collagen type I in biological specimens

被引:83
作者
Capella-Monsonis, Hector [1 ,2 ]
Coentro, Joao Q. [1 ,2 ]
Graceffa, Valeria [1 ,2 ]
Wu, Zhuning [1 ,2 ]
Zeugolis, Dimitrios I. [1 ,2 ]
机构
[1] Natl Univ Ireland Galway, Regenerat Modular & Dev Engn Lab REMODEL, Galway, Ireland
[2] Natl Univ Ireland Galway, SFI, Ctr Res Med Devices CURAM, Galway, Ireland
基金
爱尔兰科学基金会; 欧盟地平线“2020”;
关键词
RAT TAIL TENDON; AMINO-ACID ANALYSIS; CONNECTIVE-TISSUE; CROSS-LINKING; CHROMATOGRAPHIC FRACTIONATION; THERMAL-STABILITY; OXYGEN-TENSION; HYDROXYPROLINE; EXTRACTION; ELASTIN;
D O I
10.1038/nprot.2017.117
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Collagen type I is the most abundant extracellular matrix protein, and collagen type I supramolecular assemblies (e. g., tissue grafts, biomaterials and cell-assembled systems) are used extensively in tissue engineering and regenerative medicine. Many studies, for convenience or economic reasons, do not accurately determine collagen type I purity, concentration, solubility and extent of cross-linking in biological specimens, frequently resulting in erroneous conclusions. In this protocol, we describe solubility; normal, reduced and delayed (interrupted) SDS-PAPAGE; hydroxyproline; Sircol collagen and Pierce BCACA protein; denaturation temperature; ninhydrin/trinitrobenzene sulfonic acid; and collagenase assays and assess them in a diverse range of biological samples (e. g., tissue samples; purified solutions or lyophilized materials; 3D scaffolds, such as sponges and hydrogels; and cell media and layers). Collectively, the described protocols provide a comprehensive, yet fast and readily implemented, toolbox for collagen type I characterization in any biological specimen.
引用
收藏
页码:507 / 529
页数:23
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