Morton Leslie A, Tamura Ryo, de Jesus Armando J, Espinoza Arianna, Yin Hang
Department of Chemistry & Biochemistry and the BioFrontiers Institute, University of Colorado, Boulder, Colorado, 80309-0596, the United States of America.
Biochim Biophys Acta. 2014 Dec;1838(12):3137-3144. doi: 10.1016/j.bbamem.2014.08.027. Epub 2014 Sep 6.
Curved membranes are a common and important attribute in cells. Protein and peptide curvature sensors are known to activate signaling pathways, initiate vesicle budding, trigger membrane fusion, and facilitate molecular transport across cell membranes. Nonetheless, there is little understanding how these proteins and peptides achieve preferential binding of different membrane curvatures. The current study is to elucidate specific factors required for curvature sensing. As a model system, we employed a recently identified peptide curvature sensor, MARCKS-ED, derived from the effector domain of the myristoylated alanine-rich C kinase substrate protein, for these biophysical investigations. An atomistic molecular dynamics (MD) simulation suggested an important role played by the insertion of the Phe residues within MARCKS-ED. To test these observations from our computational simulations, we performed electron paramagnetic resonance (EPR) studies to determine the insertion depth of MARCKS-ED into differently curved membrane bilayers. Next, studies with varied lipid compositions revealed their influence on curvature sensing by MARCKS-ED, suggesting contributions from membrane fluidity, rigidity, as well as various lipid structures. Finally, we demonstrated that the curvature sensing by MARCKS-ED is configuration independent. In summary, our studies have shed further light to the understanding of how MARCKS-ED differentiates between membrane curvatures, which may be generally applicable to protein curvature sensing behavior.
弯曲膜是细胞中常见且重要的特征。已知蛋白质和肽曲率传感器可激活信号通路、引发囊泡出芽、触发膜融合并促进分子跨细胞膜运输。然而,对于这些蛋白质和肽如何实现对不同膜曲率的优先结合却知之甚少。当前的研究旨在阐明曲率传感所需的特定因素。作为一个模型系统,我们采用了一种最近鉴定出的肽曲率传感器MARCKS - ED,它源自富含肉豆蔻酰化丙氨酸的蛋白激酶C底物蛋白的效应结构域,用于这些生物物理研究。原子分子动力学(MD)模拟表明MARCKS - ED内苯丙氨酸残基的插入起着重要作用。为了验证我们计算模拟中的这些观察结果,我们进行了电子顺磁共振(EPR)研究,以确定MARCKS - ED插入不同曲率膜双层的深度。接下来,对不同脂质组成的研究揭示了它们对MARCKS - ED曲率传感的影响,表明膜流动性、刚性以及各种脂质结构都有贡献。最后,我们证明了MARCKS - ED的曲率传感与构型无关。总之,我们的研究进一步阐明了MARCKS - ED如何区分膜曲率,这可能普遍适用于蛋白质曲率传感行为。