结蛋白
线粒体通透性转换孔
线粒体
生物
MPTP公司
蛋白质组学
蛋白质组
免疫染色
线粒体膜转运蛋白
细胞生物学
粒线体疾病
线粒体凋亡诱导通道
分子生物学
线粒体DNA
生物化学
细胞凋亡
线粒体内膜
免疫组织化学
程序性细胞死亡
神经科学
免疫学
波形蛋白
多巴胺能
多巴胺
基因
作者
Yunqing Chen,Junjun Zheng,Shu-Yun Chen,Min Zhu,Daojun Hong
摘要
To investigate the underlying mechanisms of how the defects of desmin cause mitochondrial abnormalities in desminopathy.Primary myoblasts were isolated from muscle biopsy of a desminopathy patient with mitochondrial abnormalities. Two-dimensional gel electrophoresis analyses of mitochondrial proteins were performed in mitochondria isolated from myoblasts. Immunostaining, immunoblot, and mitochondrial function tests were carried out to confirm the proteomic results.42 proteins were found with significant expression differences in the mitochondrial proteomics. Several proteins associated with regulation of the mitochondrial permeability transition pore (MPTP) complex were identified in functional cluster analysis. The patterns of protein expression were also confirmed by strong immunoreactivity, increased MPTP opening and elevated level of oxidative stress.The study provides an overall perspective of the mitochondrial proteome plasticity in a case of desminopathy with mitochondrial abnormalities. The expression patterns of protein associated with MPTP indicate that desmin might affect MPTP complex as potential targets involved in mitochondrial dysfunction in desminopathy. However, the precise underlying mechanism remains to be elucidated. .
科研通智能强力驱动
Strongly Powered by AbleSci AI