Brezovsky Jan, Kozlikova Barbora, Damborsky Jiri
Loschmidt Laboratories, Department of Experimental Biology, Research Centre for Toxic Compounds in the Environment RECETOX, Faculty of Science, Masaryk University, Kamenice 5/A13, 625 00, Brno, Czech Republic.
Human Computer Interaction Laboratory, Faculty of Informatics, Masaryk University, Botanicka 68a, 602 00, Brno, Czech Republic.
Methods Mol Biol. 2018;1685:25-42. doi: 10.1007/978-1-4939-7366-8_3.
Protein tunnels connecting the functional buried cavities with bulk solvent and protein channels, enabling the transport through biological membranes, represent the structural features that govern the exchange rates of ligands, ions, and water solvent. Tunnels and channels are present in a vast number of known proteins and provide control over their function. Modification of these structural features by protein engineering frequently provides proteins with improved properties. Here we present a detailed computational protocol employing the CAVER software that is applicable for: (1) the analysis of tunnels and channels in protein structures, and (2) the selection of hot-spot residues in tunnels or channels that can be mutagenized for improved activity, specificity, enantioselectivity, or stability.
连接功能性埋藏腔与大量溶剂和蛋白质通道的蛋白质隧道,能够实现生物膜的运输,代表了控制配体、离子和水溶剂交换速率的结构特征。隧道和通道存在于大量已知蛋白质中,并对其功能进行调控。通过蛋白质工程对这些结构特征进行修饰,常常能赋予蛋白质更好的特性。在此,我们展示了一种详细的计算方案,该方案采用CAVER软件,适用于:(1)分析蛋白质结构中的隧道和通道,以及(2)选择隧道或通道中可进行诱变以提高活性、特异性、对映选择性或稳定性的热点残基。