Agbas Abdulbaki, Krishnamurthy Partha, Michaelis Mary L, Michaelis Elias K
Department of Biosciences, Kansas City University of Medicine and Biosciences, Kansas City, Missouri.
Department of Pharmacology, Toxicology & Therapeutics, University of Kansas Medical Center, Kansas City, Kansas.
Curr Protoc Toxicol. 2019 Jun;80(1):e73. doi: 10.1002/cptx.73. Epub 2019 Apr 5.
Measurement of the electron transfer cascade (ETC) enzyme activities and their kinetic profiles is important in assessing mitochondrial function in the nervous system in health and disease or following exposure to toxic agents. The optimization of enzymatic assays for brain tissues and neurons is critical to the development of high-throughput assay formats. This article describes a step-by-step protocol for reliable and reproducible assessment of ETC enzyme kinetics (Complex I-IV) for mitochondria from small quantities of tissue from different brain regions, such as the hippocampus, cerebellum, and frontal cortex, or from neurons in culture. Methods for differential and density gradient centrifugation are detailed for isolating cell body and synaptic mitochondria from brain, as well as measurement of ETC activities in microwell plate or single-cuvette format using spectrophotometric methods. Easy-to follow assay layouts and useful tips are presented, allowing the user to perform these assays in under 3 hr. © 2019 by John Wiley & Sons, Inc.
测量电子传递链(ETC)酶活性及其动力学曲线对于评估健康和疾病状态下或接触有毒物质后神经系统中的线粒体功能非常重要。优化针对脑组织和神经元的酶促测定方法对于高通量测定形式的发展至关重要。本文介绍了一种逐步方案,用于可靠且可重复地评估来自不同脑区(如海马体、小脑和额叶皮质)的少量组织或培养神经元中的线粒体的ETC酶动力学(复合体I-IV)。详细介绍了用于从大脑中分离细胞体和突触线粒体的差速离心和密度梯度离心方法,以及使用分光光度法在微孔板或单比色皿形式下测量ETC活性的方法。文中给出了易于遵循的测定布局和实用提示,使用户能够在3小时内完成这些测定。© 2019约翰威立国际出版公司