Hirokawa N
Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, Japan 113.
Curr Opin Neurobiol. 1997 Oct;7(5):605-14. doi: 10.1016/s0959-4388(97)80079-7.
Progress in the identification and characterization of new carboxy-terminal motor domain type kinesin superfamily proteins (KIFs)-KIFC2, 16 new KIFs and KIF-associated protein 3 (KAP3)-has provided further insight into the molecular mechanisms of organelle transport in neurons. Developments in molecular and cellular biophysics and recombinant adenovirus infection techniques combined with transgenic mice technology have enhanced the visualization of moving forms of cytoskeletal proteins during slow transport. The results of these studies strongly support the subunit transport theory.
新的羧基末端运动结构域型驱动蛋白超家族蛋白(KIFs)——KIFC2、16种新的KIFs以及KIF相关蛋白3(KAP3)的鉴定和特性研究取得了进展,这为深入了解神经元中细胞器运输的分子机制提供了更多线索。分子与细胞生物物理学以及重组腺病毒感染技术的发展,结合转基因小鼠技术,增强了对慢速运输过程中细胞骨架蛋白移动形式的可视化。这些研究结果有力地支持了亚基运输理论。