Ostermann J
European Molecular Biology Laboratory, Cell Biology Program, Meyerhofstrasse 1, 69117 Heidelberg, Germany.
EMBO Rep. 2001 Apr;2(4):324-9. doi: 10.1093/embo-reports/kve067.
The in vitro complementation assay established by Rothman and co-workers continues to be an important tool to study intra-Golgi transport. In this study, kinetic modeling is used to identify four main parameters that, together, explain the basic features of an assay that is a modification of the original assay. First, the assay signal depends on the ratio of Golgi membranes to transport intermediates in the assay. Secondly, an inactivation rate describes how the activity of transport intermediates decreases over time. Thirdly, the rate at which transport intermediates irreversibly bind to Golgi membranes is measured independently of membrane fusion, thus allowing a quantitative distinction between these two steps. Fourthly, a single rate constant describes the remaining reactions, which result in membrane fusion. This approach of kinetic modeling of experiments is generally applicable to other in vitro assays of cell biological phenomena, permitting quantitative interpretations and an increased resolution of the experiments.
罗斯曼及其同事建立的体外互补分析方法仍然是研究高尔基体内部运输的重要工具。在本研究中,动力学建模用于识别四个主要参数,这些参数共同解释了对原始分析方法进行修改后的一种分析方法的基本特征。首先,分析信号取决于分析中高尔基体膜与运输中间体的比例。其次,失活速率描述了运输中间体的活性如何随时间降低。第三,运输中间体不可逆地与高尔基体膜结合的速率是独立于膜融合来测量的,从而能够对这两个步骤进行定量区分。第四,一个单一的速率常数描述了导致膜融合的其余反应。这种对实验进行动力学建模的方法通常适用于其他细胞生物学现象的体外分析,从而实现定量解释并提高实验分辨率。