Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
Centre for Statistical Data Analysis, European Molecular Biology Laboratory, Heidelberg, Germany.
Mol Syst Biol. 2017 Dec 18;13(12):962. doi: 10.15252/msb.20177608.
Nuclear transport receptors (NTRs) recognize localization signals of cargos to facilitate their passage across the central channel of nuclear pore complexes (NPCs). About 30 different NTRs constitute different transport pathways in humans and bind to a multitude of different cargos. The exact cargo spectrum of the majority of NTRs, their specificity and even the extent to which active nucleocytoplasmic transport contributes to protein localization remains understudied because of the transient nature of these interactions and the wide dynamic range of cargo concentrations. To systematically map cargo-NTR relationships , we used proximity ligation coupled to mass spectrometry (BioID). We systematically fused the engineered biotin ligase BirA* to 16 NTRs. We estimate that a considerable fraction of the human proteome is subject to active nuclear transport. We quantified the specificity and redundancy in NTR interactions and identified transport pathways for cargos. We extended the BioID method by the direct identification of biotinylation sites. This approach enabled us to identify interaction interfaces and to discriminate direct versus piggyback transport mechanisms. Data are available via ProteomeXchange with identifier PXD007976.
核转运受体 (NTRs) 识别货物的定位信号,以促进它们穿过核孔复合体 (NPCs) 的中央通道。大约 30 种不同的 NTRs 在人类中构成不同的运输途径,并与多种不同的货物结合。由于这些相互作用的瞬时性质和货物浓度的广泛动态范围,大多数 NTRs 的精确货物谱、它们的特异性甚至主动核质转运对蛋白质定位的贡献程度仍未得到充分研究。为了系统地绘制货物-NTR 关系图,我们使用了与质谱相结合的邻近连接 (BioID)。我们系统地将工程化的生物素连接酶 BirA* 融合到 16 个 NTRs 中。我们估计人类蛋白质组的相当一部分受到主动核转运的影响。我们量化了 NTR 相互作用的特异性和冗余性,并确定了货物的运输途径。我们通过直接鉴定生物素化位点扩展了 BioID 方法。这种方法使我们能够识别相互作用界面,并区分直接和搭便车运输机制。数据可通过 ProteomeXchange 获取,标识符为 PXD007976。