Regenerative, Modular & Developmental Engineering Laboratory (REMODEL), National University of Ireland Galway (NUI Galway), Galway, Ireland.
Science Foundation Ireland (SFI) Centre for Research in Medical Devices (CÚRAM), National University of Ireland Galway (NUI Galway), Galway, Ireland.
Nat Protoc. 2018 Mar;13(3):507-529. doi: 10.1038/nprot.2017.117. Epub 2018 Feb 15.
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-PAGE; hydroxyproline; Sircol collagen and Pierce BCA 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.
I 型胶原是最丰富的细胞外基质蛋白,I 型胶原超分子组装体(例如组织移植物、生物材料和细胞组装系统)广泛用于组织工程和再生医学。出于方便或经济原因,许多研究并未准确确定生物样本中 I 型胶原的纯度、浓度、溶解度和交联程度,这经常导致错误的结论。在本方案中,我们描述了溶解度、正常、还原和延迟(中断)SDS-PAGE、羟脯氨酸、Sircol 胶原和 Pierce BCA 蛋白、变性温度、茚三酮/三硝基苯磺酸和胶原酶测定,并在各种生物样本(例如组织样本、纯化溶液或冻干材料、3D 支架,如海绵和水凝胶以及细胞培养基和层)中对其进行评估。总的来说,所描述的方案为任何生物样本中 I 型胶原的特征提供了一个全面、快速且易于实施的工具包。