Bahl Kriti, Naslavsky Naava, Caplan Steve
Department of Biochemistry and Molecular Biology, the Fred and Pamela Buffett Cancer Center, The University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
PLoS One. 2015 Apr 15;10(4):e0123710. doi: 10.1371/journal.pone.0123710. eCollection 2015.
The C-terminal Eps 15 Homology Domain proteins (EHD1-4) play important roles in regulating endocytic trafficking. EHD2 is the only family member whose crystal structure has been solved, and it contains an unstructured loop consisting of two proline-phenylalanine (PF) motifs: KPFRKLNPF. In contrast, despite EHD2 having nearly 70% amino acid identity with its paralogs, EHD1, EHD3 and EHD4, the latter proteins contain a single KPF or RPF motif, but no NPF motif. In this study, we sought to define the precise role of each PF motif in EHD2's homo-dimerization, binding with the protein partners, and subcellular localization. To test the role of the NPF motif, we generated an EHD2 NPF-to-NAF mutant to mimic the homologous sequences of EHD1 and EHD3. We demonstrated that this mutant lost both its ability to dimerize and bind to Syndapin2. However, it continued to localize primarily to the cytosolic face of the plasma membrane. On the other hand, EHD2 NPF-to-APA mutants displayed normal dimerization and Syndapin2 binding, but exhibited markedly increased nuclear localization and reduced association with the plasma membrane. We then hypothesized that the single PF motif of EHD1 (that aligns with the KPF of EHD2) might be responsible for both binding and localization functions of EHD1. Indeed, the EHD1 RPF motif was required for dimerization, interaction with MICAL-L1 and Syndapin2, as well as localization to tubular recycling endosomes. Moreover, recycling assays demonstrated that EHD1 RPF-to-APA was incapable of supporting normal receptor recycling. Overall, our data suggest that the EHD2 NPF phenylalanine residue is crucial for EHD2 localization to the plasma membrane, whereas the proline residue is essential for EHD2 dimerization and binding. These studies support the recently proposed model in which the EHD2 N-terminal region may regulate the availability of the unstructured loop for interactions with neighboring EHD2 dimers, thus promoting oligomerization.
C末端Eps 15同源结构域蛋白(EHD1 - 4)在调节内吞运输中发挥重要作用。EHD2是该家族中唯一晶体结构已被解析的成员,它包含一个由两个脯氨酸 - 苯丙氨酸(PF)基序组成的无结构环:KPFRKLNPF。相比之下,尽管EHD2与其旁系同源物EHD1、EHD3和EHD4具有近70%的氨基酸同一性,但后三者仅包含一个KPF或RPF基序,而没有NPF基序。在本研究中,我们试图确定每个PF基序在EHD2的同源二聚化、与蛋白伴侣结合以及亚细胞定位中的精确作用。为了测试NPF基序的作用,我们构建了一个EHD2 NPF突变为NAF的突变体,以模拟EHD1和EHD3的同源序列。我们证明该突变体失去了二聚化和与Syndapin2结合的能力。然而,它仍主要定位于质膜的胞质面。另一方面,EHD2 NPF突变为APA的突变体表现出正常的二聚化和与Syndapin2的结合,但核定位显著增加,与质膜的结合减少。然后我们推测EHD1的单个PF基序(与EHD2的KPF对齐)可能负责EHD1的结合和定位功能。事实上,EHD1的RPF基序对于二聚化、与MICAL - L1和Syndapin2的相互作用以及定位于管状循环内体是必需的。此外,回收实验表明EHD1 RPF突变为APA无法支持正常的受体回收。总体而言,我们的数据表明EHD2的NPF苯丙氨酸残基对于EHD2定位于质膜至关重要,而脯氨酸残基对于EHD2的二聚化和结合必不可少。这些研究支持了最近提出的模型,即EHD2的N末端区域可能调节无结构环与相邻EHD2二聚体相互作用的可用性,从而促进寡聚化。