Patel Nirav, Ramachandran Srinivasan, Azimov Rustam, Kagan Bruce L, Lal Ratnesh
Departments of Bioengineering and Mechanical & Aerospace Engineering, University of California at San Diego , La Jolla, California 92093, United States.
Department of Psychiatry, David Geffen School of Medicine, Semel Institute for Neuroscience & Human Behavior, University of California , Los Angeles, California 90095, United States.
Biochemistry. 2015 Dec 22;54(50):7320-5. doi: 10.1021/acs.biochem.5b00988. Epub 2015 Dec 7.
Tau is a microtubule associated protein implicated in the pathogenesis of several neurodegenerative diseases. Because of the channel forming properties of other amyloid peptides, we employed planar lipid bilayers and atomic force microscopy to test tau for its ability to form ion permeable channels. Our results demonstrate that tau can form such channels, but only under acidic conditions. The channels formed are remarkably similar to amyloid peptide channels in their appearance, physical and electrical size, permanence, lack of ion selectivity, and multiple channel conductances. These channels differ from amyloid channels in their voltage dependence and resistance to blockade by zinc ion. These channels could explain tau's pathologic role in disease by lowering membrane potential, dysregulating calcium, depolarizing mitochondria, or depleting energy stores. Tau might also combine with amyloid beta peptides to form toxic channels.
tau蛋白是一种与微管相关的蛋白质,与多种神经退行性疾病的发病机制有关。鉴于其他淀粉样肽具有形成通道的特性,我们利用平面脂质双分子层和原子力显微镜来检测tau蛋白形成离子通透通道的能力。我们的结果表明,tau蛋白能够形成此类通道,但仅在酸性条件下。所形成的通道在外观、物理和电学尺寸、持久性、缺乏离子选择性以及多种通道电导方面与淀粉样肽通道极为相似。这些通道在电压依赖性和对锌离子阻断的抗性方面与淀粉样通道不同。这些通道可能通过降低膜电位、失调钙、使线粒体去极化或耗尽能量储备来解释tau蛋白在疾病中的病理作用。tau蛋白也可能与β淀粉样肽结合形成有毒通道。