Yigit Sezin, Yu Hongtao, An Bo, Hamaia Samir, Farndale Richard W, Kaplan David L, Lin Yu-Shan, Brodsky Barbara
From the Departments of Biomedical Engineering and Chemistry, Tufts University, Medford, Massachusetts 02155 and.
From the Departments of Biomedical Engineering and.
J Biol Chem. 2016 Sep 2;291(36):19196-207. doi: 10.1074/jbc.M116.726182. Epub 2016 Jul 18.
The replacement of one Gly in the essential repeating tripeptide sequence of the type I collagen triple helix results in the dominant hereditary bone disorder osteogenesis imperfecta. The mechanism leading to pathology likely involves misfolding and autophagy, although it has been hypothesized that some mutations interfere with known collagen interactions. Here, the effect of Gly replacements within and nearby the integrin binding GFPGER sequence was investigated using a recombinant bacterial collagen system. When a six-triplet human type I collagen sequence containing GFPGER was introduced into a bacterial collagen-like protein, this chimeric protein bound to integrin. Constructs with Gly to Ser substitutions within and nearby the inserted human sequence still formed a trypsin-resistant triple helix, suggesting a small local conformational perturbation. Gly to Ser mutations within the two Gly residues in the essential GFPGER sequence prevented integrin binding and cell attachment as predicted from molecular dynamics studies of the complex. Replacement of Gly residues C-terminal to GFPGER did not affect integrin binding. In contrast, Gly replacements N-terminal to the GFPGER sequence, up to four triplets away, decreased integrin binding and cell adhesion. This pattern suggests either an involvement of the triplets N-terminal to GFPGER in initial binding or a propagation of the perturbation of the triple helix C-terminal to a mutation site. The asymmetry in biological consequences relative to the mutation site may relate to the observed pattern of osteogenesis imperfecta mutations near the integrin binding site.
I型胶原蛋白三螺旋结构中必需的重复三肽序列中的一个甘氨酸被替换,会导致显性遗传性骨疾病成骨不全症。尽管有人推测某些突变会干扰已知的胶原蛋白相互作用,但导致病理的机制可能涉及错误折叠和自噬。在这里,使用重组细菌胶原蛋白系统研究了整合素结合序列GFPGER及其附近的甘氨酸替换的影响。当将包含GFPGER的六联体人I型胶原蛋白序列引入细菌类胶原蛋白中时,这种嵌合蛋白与整合素结合。在插入的人类序列及其附近将甘氨酸替换为丝氨酸的构建体仍形成抗胰蛋白酶的三螺旋结构,表明存在小的局部构象扰动。如从复合物的分子动力学研究预测的那样,必需的GFPGER序列中两个甘氨酸残基内的甘氨酸到丝氨酸突变阻止了整合素结合和细胞附着。GFPGER序列C末端的甘氨酸残基替换不影响整合素结合。相反,GFPGER序列N末端的甘氨酸替换,距离可达四个三联体,会降低整合素结合和细胞粘附。这种模式表明,GFPGER序列N末端的三联体可能参与初始结合,或者三螺旋结构C末端的扰动传播到突变位点。相对于突变位点的生物学后果的不对称性可能与整合素结合位点附近观察到的成骨不全症突变模式有关。