于冬梅

(副研究员)


教师姓名:于冬梅
教师拼音名称:yudongmei
入职时间:2020-09-14
所在单位:机电与信息工程学院
学历:博士研究生毕业
性别:女
联系方式:yudongmei@sdu.edu.cn
学位:理学博士学位
职称:副研究员
在职信息:在职
毕业院校:美国密苏里大学哥伦比亚分校
学科:计算机科学与技术

论文成果

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Structural modeling, mutation analysis, and in vitro expression of usherin, a major protein in inherited retinal degeneration and hearing loss

发布时间:2021-03-26 点击次数:

论文名称:Structural modeling, mutation analysis, and in vitro expression of usherin, a major protein in inherited retinal degeneration and hearing loss
发表刊物:Comput Struct Biotechnol J.
关键字:Protein folding, Recombinant protein expression, Photoreceptor, Hair cell, Structural model, Cell adhesion, Membrane protein, Usher syndrome, Retinitis pigmentosa
摘要:Usherin is the most common causative protein associated with autosomal recessive retinitis pigmentosa (RP) and Usher syndrome (USH), which are characterized by retinal degeneration alone and in combination with hearing loss, respectively. Usherin is essential for photoreceptor survival and hair cell bundle integrity. However, the molecular mechanism underlying usherin function in normal and disease conditions is unclear. In this study, we investigated structural models of usherin domains and localization of usherin pathogenic small in-frame mutations, mainly homozygous missense mutations. We found that usherin fibronectin III (FN3) domains and most laminin-related domains have a β-sandwich structure. Some FN3 domains are predicted to interact with each other and with laminin-related domains. The usherin protein may bend at some FN3 linker regions. RP- and USH-associated small in-frame mutations are differentially located in usherin domains. Most of them are located at the periphery of β-sandwiches, with some at the interface between interacting domains. The usherin laminin epidermal growth factor repeats adopt a rod-shaped structure, which is maintained by disulfide bonds. Most missense mutations and deletion of exon 13 in this region disrupt the disulfide bonds and may affect local protein folding. Despite low expression of the recombinant entire protein and protein fragments in mammalian cell culture, usherin FN3 fragments are more robustly expressed and secreted than its laminin-related fragments. Our findings provide new insights into the usherin structure and the disease mechanisms caused by pathogenic small in-frame mutations, which will help inform future experimental research on diagnosis, disease mechanisms, and therapeutic approaches.
学科门类:工学
是否译文:
发表时间:2020-06-01
收录刊物:SCI
发表时间:2020-06-01