Wu Jingyi, Wang Xiaofang
Department of Biomedical Sciences and Center for Craniofacial Research and Diagnosis, Texas A&M University College of Dentistry, Dallas, TX, USA.
Stomatological Hospital, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.
Methods Mol Biol. 2019;1922:211-218. doi: 10.1007/978-1-4939-9012-2_21.
The extracellular matrix of the bone and dentin contains several non-collagenous proteins (NCPs). One category of NCPs is termed the SIBLING (small integrin-binding ligand, N-linked glycoprotein) family, which includes osteopontin (OPN), bone sialoprotein (BSP), dentin matrix protein 1 (DMP1), dentin sialophosphoprotein (DSPP), etc. These proteins have abundant phosphoserines, aspartic acids, and glutamic acids. In this protocol, we describe the extraction of NCPs from the bone and dentin matrices using guanidine-HCl/EDTA and the isolation of polyanionic SIBLINGs from NCPs using ion-exchange fast protein liquid chromatography (FPLC) to separate the differentially charged proteins into different fractions through a gradient elution by NaCl.
骨骼和牙本质的细胞外基质包含多种非胶原蛋白(NCPs)。一类NCPs被称为SIBLING(小整合素结合配体,N-连接糖蛋白)家族,其中包括骨桥蛋白(OPN)、骨涎蛋白(BSP)、牙本质基质蛋白1(DMP1)、牙本质涎磷蛋白(DSPP)等。这些蛋白质含有丰富的磷酸丝氨酸、天冬氨酸和谷氨酸。在本实验方案中,我们描述了使用盐酸胍/乙二胺四乙酸从骨骼和牙本质基质中提取NCPs,并使用离子交换快速蛋白质液相色谱(FPLC)从NCPs中分离多阴离子SIBLINGs,通过氯化钠梯度洗脱将带不同电荷的蛋白质分离到不同的组分中。