Svensson Bengt, Autry Joseph M, Thomas David D
Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, 6-155 Jackson Hall, 321 Church St., Minneapolis, MN, 55455, USA.
Methods Mol Biol. 2016;1377:503-22. doi: 10.1007/978-1-4939-3179-8_42.
Molecular modeling and simulation are useful tools in structural biology, allowing the formulation of functional hypotheses and interpretation of spectroscopy experiments. Here, we describe a method to construct in silico models of a fluorescent fusion protein construct, where a cyan fluorescent protein (CFP) is linked to the actuator domain of the Sarco/Endoplasmic Reticulum Ca(2+)-ATPase (SERCA). This CFP-SERCA construct is a biosensor that can report on structural dynamics in the cytosolic headpiece of SERCA. Molecular modeling and FRET experiments allow us to generate new structural and mechanistic models that better describe the conformational landscape and regulation of SERCA. The methods described here can be applied to the creation of models for any fusion protein constructs and also describe the steps needed to simulate FRET results using molecular models.
分子建模和模拟是结构生物学中有用的工具,有助于形成功能假设并解释光谱实验结果。在此,我们描述了一种构建荧光融合蛋白构建体计算机模型的方法,其中青色荧光蛋白(CFP)与肌浆网/内质网Ca(2+) -ATP酶(SERCA)的驱动结构域相连。这种CFP-SERCA构建体是一种生物传感器,可报告SERCA胞质头部的结构动力学。分子建模和荧光共振能量转移(FRET)实验使我们能够生成新的结构和机制模型,从而更好地描述SERCA的构象变化情况及其调控机制。这里描述的方法可应用于创建任何融合蛋白构建体的模型,还介绍了使用分子模型模拟FRET结果所需的步骤。