Volume 3, Issue 1, Pages (January 2013)

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Volume 3, Issue 1, Pages 30-35 (January 2013) Structure of a Pestivirus Envelope Glycoprotein E2 Clarifies Its Role in Cell Entry  Kamel El Omari, Oleg Iourin, Karl Harlos, Jonathan M. Grimes, David I. Stuart  Cell Reports  Volume 3, Issue 1, Pages 30-35 (January 2013) DOI: 10.1016/j.celrep.2012.12.001 Copyright © 2013 The Authors Terms and Conditions

Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure 1 Overall Fold of BVDV1 E2 (A) Cartoon representation of the crystal structure of BVDV1 E2 obtained at pH8. A dimer of BVDV1 E2 is seen in the crystal. Domains of monomer A starting from the N terminus are colored in blue, green, yellow and red, respectively. The sugars are shown as magenta sticks and disulfide bridges are represented as cyan spheres. (B) Linear representation of BVDV1 E2 showing the four domains DA, DB, DC and DD with their domain boundaries. Coloring as in a. (C) Cartoon representation of the crystal structure of BVDV1 E2 obtained at pH5. Domains DA of monomers A and B are disordered (the transparent surface rendered shows the position of the domains when ordered at higher pH). See also Figures S1, S2, S3, and S4. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure 2 Mapping of Epitopes of Classical Swine Fever Virus E2 onto the Structure of BVDV E2 (A) Cartoon representation of a monomer of BVDV1 E2 colored by domain as in Figure 1. (B) Positions of the antigenic regions A and B/C. (C) Location of the linear epitopes LFDGTNP (orange) and TAVSPTTLR (cyan). LFDGTNP is at the border of the two antigenic regions, whereas TAVSPTTLR is located in the antigenic region A. See also Figure S1. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure 3 Interactions of BVDV1 E2 and Their Locations (A) Location of histidine (H70) of domain DA, which is conserved among pestiviruses and that may trigger an order-disorder transition of this domain at low pH. (B) The potential host cell receptor binding site in domain DB colored in pink. Domain DB is rotated as shown. (C) The interface of monomers A (shown colored) and B (shown in gray) contains a strand swap and hydrophobic residues such as phenylalanines, tyrosines and tryptophanes drawn as sticks. Domains DD of molecules A and B are linked by a disulfide bridge (cyan sphere) to form a covalent homodimer. See also Figure S1. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure 4 Proposed Model of the Fusion Mechanism of Pestiviruses A covalently linked E1-E2 heterodimer is present on the viral membrane. E2 binds to the host receptor (possibly CD46, shown in light blue) through domain DB prior to endocytosis. As CD46 is not internalized, a putative secondary receptor (transparent) presumably replaces CD46. Throughout this process the putative fusion loop of E1 (magenta), is concealed by domain DA of E2. At low pH, domain DA of E2 becomes disordered and exposes the fusion loop that will then be able to insert into the endosome membrane and trigger membrane fusion. It is as yet unknown whether E1 forms trimers as seen for other fusion proteins. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure S1 Amino Acid Conservation between Pestiviruses E2 Glycoprotein, Related to Figures 1, 2, and 3 (A) Sequence alignment of BVDV1 E2 with E2 proteins from other pestiviruses: BVDV2, BVDV3, Classical Swine Fever virus (CSFV), Border Disease virus (BDV), Pestivirus of giraffe (gir) and Bungowannah virus (bung). Conserved residues are drawn in red boxes, similar residues in red type. The secondary structure assignment for BVDV1 E2 is shown at the top and domains DA, DB, DC and DD are colored in blue, green, yellow and red, respectively. Cysteines involved in intra-chain disulfide bridges are marked by a green number, the single cysteine involved in the inter-chain disulfide bridge is marked by a green square, the four glycosylation sites of BVDV1 E2 are marked with magenta squares and the conserved histidine is marked with a cyan square. (B) Surface representation of a monomer of BVDV E2 colored according to sequence conservation from white (non-conserved) to red (conserved). Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure S2 Domains DA and DB Have Ig-fold, Related to Figure 1 (A) Domain DA of BVDV1 E2 (neutral pH form) is colored in blue and is superimposed on a T cell receptor alpha chain (PDB: 2Z31, Z = 5.3, rmsd = 2.8Å) colored in orange. (B) Domain DB is colored in green and is superimposed on the C-terminal domain of semaphorin 4D (PDB: 1OLZ, Z = 6.7, rmsd = 2.3Å) colored in pink. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure S3 Stability of BVDV1 E2 Domains over pH, Related to Figure 1 (A) domain DA stability depends on pH, the results would suggest that domain become less stable when moving from physiological pH (7.4) to the endosome pH 5. (B) For comparison, domain DB, a similarly sized Ig-like domain to domain DA, would not be destabilized by a change of pH from 7.4 to 5. (C) Domains DB-DC-DD would not be destabilized by a change of pH from 7.4 to 5. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions

Figure S4 Structural Comparison of Pestivirus and Alphavirus E2 Glycoproteins at High and Low pH, Related to Figure 1 (A) Cartoon representation of the crystal structures of BVDV E2 at high (left) and low pH (right) colored as defined in Figure 1. (B) Cartoon representation of the crystal structures of CHIKV E2 obtained at high pH (left) and sindbis virus E2 obtained at low pH (right). The Ig domains A, B, C are colored in blue, green and yellow respectively. The linker domain is colored in gray. Cell Reports 2013 3, 30-35DOI: (10.1016/j.celrep.2012.12.001) Copyright © 2013 The Authors Terms and Conditions