Hagen Christoph, Dent Kyle C, Zeev-Ben-Mordehai Tzviya, Grange Michael, Bosse Jens B, Whittle Cathy, Klupp Barbara G, Siebert C Alistair, Vasishtan Daven, Bäuerlein Felix J B, Cheleski Juliana, Werner Stephan, Guttmann Peter, Rehbein Stefan, Henzler Katja, Demmerle Justin, Adler Barbara, Koszinowski Ulrich, Schermelleh Lothar, Schneider Gerd, Enquist Lynn W, Plitzko Jürgen M, Mettenleiter Thomas C, Grünewald Kay
Oxford Particle Imaging Centre, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
Oxford Particle Imaging Centre, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK; Diamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot OX11 0DE, UK.
Cell. 2015 Dec 17;163(7):1692-701. doi: 10.1016/j.cell.2015.11.029.
Vesicular nucleo-cytoplasmic transport is becoming recognized as a general cellular mechanism for translocation of large cargoes across the nuclear envelope. Cargo is recruited, enveloped at the inner nuclear membrane (INM), and delivered by membrane fusion at the outer nuclear membrane. To understand the structural underpinning for this trafficking, we investigated nuclear egress of progeny herpesvirus capsids where capsid envelopment is mediated by two viral proteins, forming the nuclear egress complex (NEC). Using a multi-modal imaging approach, we visualized the NEC in situ forming coated vesicles of defined size. Cellular electron cryo-tomography revealed a protein layer showing two distinct hexagonal lattices at its membrane-proximal and membrane-distant faces, respectively. NEC coat architecture was determined by combining this information with integrative modeling using small-angle X-ray scattering data. The molecular arrangement of the NEC establishes the basic mechanism for budding and scission of tailored vesicles at the INM.
囊泡核质运输正逐渐被视为一种将大分子货物转运穿过核膜的普遍细胞机制。货物被招募,在内核膜(INM)处被包裹,并通过外核膜处的膜融合进行递送。为了理解这种运输的结构基础,我们研究了子代疱疹病毒衣壳的核输出,其中衣壳包裹由两种病毒蛋白介导,形成核输出复合体(NEC)。使用多模态成像方法,我们在原位观察到NEC形成了特定大小的被膜小泡。细胞电子冷冻断层扫描显示,在其膜近端和膜远端表面分别有一层呈现两种不同六边形晶格的蛋白质层。通过将这些信息与使用小角X射线散射数据的整合建模相结合,确定了NEC被膜结构。NEC的分子排列建立了在内核膜处形成定制小泡并进行出芽和分裂的基本机制。