驱动蛋白
轴浆运输
遗传性痉挛性截瘫
神经科学
肌萎缩侧索硬化
运动蛋白
突触
生物
微管
细胞生物学
医学
病理
疾病
生物化学
基因
表型
作者
Kumiko Hayashi,Kazuo Sasaki
标识
DOI:10.1016/j.neures.2023.09.004
摘要
Kinesin motor proteins play crucial roles in anterograde transport of cargo vesicles in neurons, moving them along axons from the cell body towards the synaptic region. Not only the transport force and velocity of single motor protein, but also the number of kinesin molecules involved in transporting a specific cargo, is pivotal for synapse formation. This collective transport by multiple kinesins ensures stable and efficient cargo transport in neurons. Abnormal increases or decreases in the number of engaged kinesin molecules per cargo could potentially act as biomarkers for neurodegenerative diseases such as Alzheimer's, Parkinson's, amyotrophic lateral sclerosis (ALS), spastic paraplegia, polydactyly syndrome, and virus transport disorders. We review here a model constructed using physical measurements to quantify the number of kinesin molecules associated with their cargo, which could shed light on the molecular mechanisms of neurodegenerative diseases related to axonal transport.
科研通智能强力驱动
Strongly Powered by AbleSci AI