Zhou Guo-Ping
Department of Chemistry, North Carolina State University, NC 27695, USA.
Protein Pept Lett. 2011 Oct;18(10):966-78. doi: 10.2174/0929866511107010966.
Physiologic relaxation of vascular smooth muscle is induced by the cyclic guanosine monophosphate (cGMP)- dependent protein kinase Iα enzyme (cGKIα), which activates myosin phosphatase (MLCP). This activation process is thought to occur through the interaction involving both N- and C-terminal leucine zipper coiled-coil (LZCC) domains of the kinase enzyme (cGKIα) with the myosin binding subunit (MBS) of MLCP. In this review, I summarize how to define the LZCC domains in both N-terminal cGKIα(1-59) and C-terminal MBS proteins using predictive and experimental methods, how to make a rapid and accurate structure determination of a cGKIα(1-59) molecule using NMR's residual dipolar coupling (RDC) measurements, and how to indentify the existence of a weak protein interaction between N-terminal LZCC domain (cGKIα(1-59)) and a LZCC domain (MBSCT42) within the C-terminal MBS. In addition, the location and orientation of the residues in LZCC proteins can be readily visualized using a novel diagram, the so-called "wenxiang diagram", which is more advantageous than traditional helical wheel diagrams in analyzing LZCC protein structures and their action mechanisms. Using the composed wenxiang diagrams, we have characterized the interaction between cGKIα(1- 59) and another LZCC molecule (MBSCT42), and deduced that the most affected residues of these two LZCC molecules might be at the positions d, a, e and g. These studies and findings are also covered in this review. It is intriguing to see that the successful incorporation of wenxiang diagrams and NMR spectroscopy in the LZCC structural and functional studies may provide some insights into protein-protein interaction mechanisms.
血管平滑肌的生理性舒张是由环磷酸鸟苷(cGMP)依赖性蛋白激酶Iα酶(cGKIα)诱导的,该酶激活肌球蛋白磷酸酶(MLCP)。这种激活过程被认为是通过激酶酶(cGKIα)的N端和C端亮氨酸拉链卷曲螺旋(LZCC)结构域与MLCP的肌球蛋白结合亚基(MBS)之间的相互作用而发生的。在这篇综述中,我总结了如何使用预测和实验方法在N端cGKIα(1-59)和C端MBS蛋白中定义LZCC结构域,如何使用核磁共振的剩余偶极耦合(RDC)测量对cGKIα(1-59)分子进行快速准确的结构测定,以及如何识别N端LZCC结构域(cGKIα(1-59))与C端MBS内的LZCC结构域(MBSCT42)之间弱蛋白相互作用的存在。此外,使用一种新颖的图表,即所谓的“文祥图”,可以很容易地可视化LZCC蛋白中残基的位置和方向,在分析LZCC蛋白结构及其作用机制方面,它比传统的螺旋轮图更具优势。使用合成的文祥图,我们已经表征了cGKIα(1-59)与另一个LZCC分子(MBSCT42)之间的相互作用,并推断这两个LZCC分子受影响最大的残基可能位于d、a、e和g位置。这些研究和发现也涵盖在本综述中。有趣的是,文祥图和核磁共振光谱在LZCC结构和功能研究中的成功结合可能为蛋白质-蛋白质相互作用机制提供一些见解。