INTRODUCTION

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Assembly of progeny virions is an essential stage in the life cycle of every virus. For double-stranded DNA viruses such as bacteriophages (4), adenoviruses (7, 9), and herpesviruses (10, 28), capsid subunits initially form a precursor capsid that is packaged with DNA and subsequently matures into an infectious particle. Assembly of the procapsid frequently requires additional proteins, termed scaffolding proteins, that are not present in the mature capsid.

The mature herpes simplex virus type 1 (HSV-1) capsid is an icosahedral shell that is 125 nm in diameter and 15 nm thick (26, 28, 29). Its major structural features are 162 capsomers (150 hexons and 12 pentons) that lie on a T=16 lattice. The capsomers associate at their proximal ends to create a 3-nm-thick floor layer. The capsomer protrusions project radially to a distance of 11 nm from the floor layer, and each capsomer has an axial channel. The major capsid protein, VP5, is the structural subunit of both the hexons and the pentons (22, 23, 38). Hexons are found on the faces and edges of the icosahedron, while one penton is found at each of the 12 capsid vertices. Two minor capsid proteins, VP19C and VP23, make up trigonal nodules called triplexes (320 in all) found just above the capsid floor layer at the local three-fold positions between adjacent capsomers (22). Triplexes may vary somewhat in composition, but on average they are heterotrimers containing one copy of VP19C and two copies of VP23 per triplex. A third minor capsid protein, VP26, is located at the outer tips of the hexons (3, 37, 40).

Assembly of the HSV-1 capsid requires an internal scaffolding protein called pre-VP22a. The major capsid protein interacts with 25 amino acids in the carboxy-terminal domain of pre-VP22a; these residues are cleaved upon release of the scaffold (14, 16, 25, 34). Although the major capsid protein and the scaffolding protein comprise the majority of the protein mass of the capsid as it is assembled, capsid assembly will not occur in the absence of the triplex proteins (6, 33, 35, 39). The triplex proteins interact with major capsid-scaffold protein complexes, forming arc- or dome-like structures called partial capsids (20). The joining of additional subunits allows partial capsids to grow into a spherical procapsid, which undergoes a morphological transition to the mature icosahedral capsid and is packaged with DNA. Three-dimensional reconstructions computed from cryoelectron micrographs of the procapsid show that it is a spherical structure that appears to be open and porous, unlike the mature capsid, which is angular and tightly sealed (20, 36). In the procapsid, the hexons are asymmetric and only loosely formed, as opposed to the symmetric, highly regular hexons in the mature capsid. In addition, the capsid floor layer, which is smooth and continuous in the mature capsid, is rudimentary and incomplete in the procapsid. Triplexes, which are visible at sites between capsomers in the procapsid, appear to be the only substantial connection between adjacent capsomers when observed at a resolution of 26 Å (36).

As described above, analysis of the procapsid structure has suggested an important role for the triplex proteins in capsid assembly. Although the triplex proteins make up a relatively small percentage of the total capsid protein, the triplexes appear to provide essential support for the capsid shell as it is formed. Here we describe use of an in vitro system comprised of insect cell extracts containing recombinant baculovirus-expressed capsid proteins to examine the role of the triplex proteins in capsid assembly. We asked whether the triplex proteins interact with the nascent capsid as separate polypeptides or as preformed structural units. In addition, we employed deletion analysis to identify domains required for triplex formation and for attachment of the triplex proteins to major capsid-scaffold protein complexes. The results shed new light on the essential role of the triplex proteins in HSV capsid assembly.

	MATERIALS AND METHODS

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Cell lines. Thomsen et al. (35) described the construction of the four recombinant baculoviruses containing the HSV-1 UL18 (encoding VP23), UL19 (VP5), UL26.5 (pre-VP22a), and UL38 (VP19C) genes employed in this study. The nonessential UL35 gene (VP26) was not included in assembly reactions. Suspension cultures of Spodoptera frugiperda (Sf9) cells were infected with individual recombinant baculoviruses (multiplicity of infection of 5), and at 64 h postinfection the cells were harvested, frozen, and diluted for use in the in vitro system as previously described (20).

In vitro capsid assembly. Cell-free capsid assembly was performed by a modification of the procedure of Newcomb et al. (21). Assembly-competent reaction mixtures contained aliquots of each of the four cell suspensions described above. Cells were lysed by five repeated cycles of freezing and thawing, and then the cellular debris was removed by centrifugation at 16,000 × g for 5 mins. The supernatant was decanted, and then EDTA (50 mM), dithiothreitol (10 mM), and protease inhibitors (20 mM phenylmethylsulfonyl fluoride, aprotinin [20 µg/ml], 10 µM leupeptin, and trypsin inhibitor [100 µg/ml]) were added. The extracts were incubated at 37°C for 30 min and clarified by centrifugation as described above. Capsids or partial capsid structures were isolated by precipitation with the VP5-specific monoclonal antibody 6F10 as described previously (20).

Construction of VP19C mutants. Deletions were made in the UL38 gene by using pAc-UL38 (35) as a template for PCRs. Upstream oligonucleotide primers were complementary to the noncoding strand and contained a BamHI restriction site. Downstream oligonucleotide primers were complementary to the coding strand and contained a KpnI restriction site. The UL38 gene was truncated by placing primers at various increments in from the 5' or 3' end of the gene. The pAc-373 vector was digested with BamHI and KpnI, gel purified, ligated to PCR products that had been digested with the same enzymes, and transformed as described previously (30). Plasmid DNA from positive clones was purified and cotransfected to generate recombinant baculoviruses (35).

Electron microscopy. Cell pellets containing capsid assembly products were prepared for electron microscopy by fixation in 2% glutaraldehyde, embedding in Epon 812, and sectioning as previously described (20). All micrographs were recorded on a JEOL 100CX transmission electron microscope operated at 80 keV.

Sucrose density gradient analysis. Sucrose gradients (5 to 20% sucrose in phosphate-buffered saline) were prepared and equilibrated to 4°C (11). Extracts containing single capsid proteins or combinations of capsid proteins were loaded onto the gradients and immediately subjected to centrifugation at 115,000 × g for 18 h at 4°C. Centrifugation was performed in a Beckman L5-50 Ultracentrifuge by using an SW50.1 rotor at 35,000 rpm, and gradients were fractionated with a Buchler Polystaltic Pump into 40 fractions of approximately 115 µl each (4 drops). Fractions were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting to identify capsid proteins. Coomassie blue-stained gels and X-ray films were digitized with a Molecular Dynamics personal densitometer, and Imagequant software was used to quantitate the capsid proteins in each lane.

Sedimentation coefficient and molecular weight determination. The calculation of sedimentation coefficients was carried out by comparison with a protein standard by the method of Martin and Ames (17). Residual bovine serum albumin (BSA) from each of the cell cultures served as an internal standard for each gradient. The position of BSA in the gradient was determined by SDS-PAGE and Western blotting. Sedimentation coefficients for capsid proteins were determined by a ratio of distance traveled by the capsid protein to distance traveled by BSA. Molecular weights were approximated from the sedimentation coefficients as described previously (17).

SDS-PAGE and Western immunoblotting. Gels were prepared with a 4% stacking gel and a 12.5% resolving gel as described previously (22). Gels were either stained with Coomassie blue or electrophoretically transferred to a nitrocellulose membrane for Western immunoblotting (30). Immunoblots were stained either with polyclonal antisera specific for VP19C and/or VP23 or with a pool of monoclonal antibodies (3N-5, 3C-16, 2-11, and 1N-11) specific for BSA. HSV-1 B capsids, used as a standard for gel electrophoresis and immunoblotting, were prepared as previously described from BHK-21 cells infected with the 17MP strain of HSV-1 (23).

	RESULTS

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In vitro assembly reactions were performed to determine whether the triplex proteins can associate with the nascent capsid independently of each other or whether the capsid assembly requires the presence of preformed triplexes. Previous studies have shown that VP5 associates with pre-VP22a in the absence of triplex proteins to form distinct structures (16). The structures are spherical, but they vary slightly in size, averaging 60 nm in diameter. These major capsid-scaffold protein complexes can be precipitated with the VP5-specific monoclonal antibody 6F10 (13). Therefore, even in the absence of capsid formation, it is possible to determine whether triplex proteins have associated with the major capsid-scaffold protein complex by examining the immunoprecipitate. Figure 1 shows SDS-PAGE and Western immunoblot analysis of assembly reaction mixtures consisting of cell extracts containing HSV-1 capsid proteins.

View larger version (48K): [in this window] [in a new window]   FIG. 1.   Protein compositions of products formed in the in vitro assembly system. Cell extracts containing recombinant VP5, pre-VP22a, VP23, and VP19C (ALL) were combined and assembly products were precipitated with the VP5-specific monoclonal antibody 6F10. The precipitate was analyzed by SDS-PAGE, and the gel was stained with Coomassie blue (a). In some reactions individual capsid proteins were omitted. Lane 1 contains HSV-1 capsids isolated from infected BHK cells as a protein standard, and lane 2 contains a reaction mixture with all four recombinant proteins. Control HSV-1 capsids from infected cells contain processed scaffolding protein (VP22a), while in vitro assembly reactions contain uncleaved scaffolding protein (pre-VP22a). Lane 3 contains ALL minus VP23, lane 4 contains ALL minus VP19C, and lane 5 contains ALL minus VP23 and VP19C. Two identical gels were blotted and probed with polyclonal antiserum specific for VP19C (b) or VP23 (c). One additional band is visible just below VP19C (panel c, lane 2); this band likely represents a breakdown product resulting from protease activity in the insect cell extract.

Control reaction mixtures contained all four baculovirus-expressed capsid proteins (VP5, pre-VP22a, VP19C, and VP23) and yielded capsids, as viewed by electron microscopy (data not shown). SDS-PAGE analysis revealed that all four capsid proteins were present in the precipitate (Fig. 1, lane 2). Western blot analysis was used to show specifically whether triplex proteins were present in each precipitate (Fig. 1b and c). VP19C, which has a molecular weight of 50,000, migrates to approximately the same position as the antibody heavy chain on the SDS gel, and thus the presence of VP19C could be detected only by immunoblotting (Fig. 1b, lane 2). A band appearing just below the antibody heavy-chain band (Fig. 1a, lanes 2 to 5) does not correspond to VP19C, as shown by the immunoblotting results (Fig. 1b), and probably represents a contaminating cellular protein. In in vitro assembly reactions, VP19C was observed to be very sensitive to proteolysis by enzymes in the cell extract, and even in the presence of protease inhibitors a breakdown product, slightly smaller than the full-length protein, is visible (Fig. 1b, lane 2). In the reaction in which VP23 was omitted, only trace amounts of VP19C were detected in the precipitate (Fig. 1b, lane 3). When VP19C was omitted from the reaction mixture, VP23 was not detected in the pellet (Fig. 1c, lane 4). Omission of both triplex proteins (lane 5) yielded a result that appeared to be identical to that observed when one protein or the other was omitted, suggesting that the triplex proteins are unable to bind to the major capsid-scaffold protein complex independently of each other.

Formation of triplexes in the absence of other capsid proteins. The possibility that triplex proteins would associate in the absence of other capsid proteins was tested by sucrose density gradient analysis. Insect cells expressing recombinant HSV proteins were lysed and clarified to obtain cell extracts containing VP19C and VP23. The cell extracts were combined and layered on top of 5 to 20% sucrose gradients prepared in phosphate-buffered saline. Cell extracts containing each protein individually were also layered onto separate gradients, and residual BSA from each cell culture served as an internal standard to ensure that differences in protein migration were not due to differences in gradient composition. Gradients were centrifuged at 115,000 × g for 18 h at 4°C. Forty fractions of 115 µl each (4 drops) were collected for each gradient. The fractions were analyzed by SDS-PAGE and Western blotting, and densitometry was used to determine the relative protein intensity for each fraction. Optical density values were normalized for each gradient and plotted versus distance from the meniscus in the gradient, as shown in Fig. 2.

View larger version (17K): [in this window] [in a new window]   FIG. 2.   Sedimentation analysis of triplex proteins and protein complexes. Cell extracts containing VP19C, VP23, or VP19C and VP23 were placed on top of 5 to 20% sucrose gradients and centrifuged for 18 h at 115,000 × g. Each gradient was fractionated, and the fractions were analyzed by SDS-PAGE and Western blotting. Protein intensity was determined with Imagequant; the values were normalized, and the relative intensity values were plotted against distance from the meniscus. BSA was included in each gradient as a standard. , VP19C;  .  . , VP23; ... ..., BSA.

Deletion analysis of VP19C. Subsequent experiments were designed to identify protein-protein interactions required for capsid assembly. The VP19C protein was truncated from either the N terminus or the C terminus by using PCR to generate shortened versions of the UL38 coding sequence. Amino acids were removed in increments of 45, 90, and 105 from the N terminus, as shown by the schematic illustration in Fig. 3a. The C terminus was shortened by 15 amino acids. Truncated proteins were expressed by using the recombinant baculovirus system, and the expression of each deletion mutant was verified by Western blotting with polyclonal antiserum specific for VP19C (Fig. 3b). Extracts containing these proteins were then substituted for extracts containing full-length VP19C in the assembly reactions described previously. The reaction mixtures contained VP5, pre-VP22a, VP23, and one of the VP19C deletion mutants. Products of assembly reactions were precipitated with the VP5-specific monoclonal antibody 6F10, and the immunoprecipitate was analyzed by Western blotting to detect the presence of VP19C mutants (Fig. 3c). Deletion of the N-terminal 45 amino acids did not affect the ability of the VP19C protein to associate with the major capsid-scaffold protein complex (Fig. 3b, lane 3). The nd90 protein was present in the precipitate; however, the amount of this protein relative to the full-length and nd45 proteins was significantly decreased (Fig. 3b, lane 4). The nd105 protein did not precipitate with the VP5-VP22a complexes, indicating that a loss of 105 amino acids from the N terminus was too great to support interaction with the assembly complex. In addition, the cd15 protein failed to precipitate (Fig. 3b, lane 6), suggesting that deletion of just 15 amino acids from the C terminus prevents interaction of VP19C with the major capsid-scaffold protein complex.

View larger version (43K): [in this window] [in a new window]   FIG. 3.   Schematic diagram illustrating the deletions made in the VP19C protein (a) and Western blot detection of VP19C deletion mutants from insect cell extracts (b) or immunoprecipitated assembly complexes (c). VP19C deletion mutants were constructed by cloning truncated genes into baculovirus vectors as described in the text. Proteins that contained deletions at the N terminus or C terminus were expressed in Sf9 cells. Whole-cell lysates were analyzed by SDS-PAGE followed by Western blotting with polyclonal antiserum specific for VP19C (b). Mutants were tested in assembly reactions that included VP5, pre-VP22a, VP23, and either full-length VP19C or one of the deletion mutants. Assembly products were precipitated with monoclonal antibody 6F10 and analyzed by Western blotting as described above (c).

View larger version (84K): [in this window] [in a new window]   FIG. 4.   Electron micrographs of capsids formed by coinfection of Sf9 cells with recombinant baculoviruses expressing VP5, pre-VP22a, VP23, and either wild-type VP19C or one of the deletion mutants. Cell pellets were fixed and thin sectioned. Capsids (arrows) were observed only in coinfections containing wild-type VP19 (a), nd45 (b), or nd90 (c). Aberrant structures (double arrows) were also seen in infections containing nd90 (c). Bar, 250 nm.

View larger version (25K): [in this window] [in a new window]   FIG. 5.   Sedimentation analysis of VP19C deletion mutants and complexes containing mutant proteins. Cell extracts containing mutant cd15 (a), nd105 (b), cd15 and VP23 (c), or nd105 and VP23 (d) were placed on top of 5 to 20% sucrose gradients and centrifuged for 18 h at 115,000 × g. Each gradient was fractionated and analyzed as described previously, with protein intensity plotted versus distance from the meniscus to show the location of protein peaks. BSA was included in each gradient as a standard. , cd15;  .  . , nd105; ... ..., BSA.

	DISCUSSION

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HSV-1 capsid assembly is a complex process in which many proteins are organized into a highly structured shell that houses and protects the viral genome. We have employed a cell-free system to demonstrate that protein interactions required for capsid assembly occur in a specific sequence. Our studies show that assembly products from reaction mixtures containing the major capsid protein, scaffold protein, and one of the two triplex proteins consist only of major capsid and scaffold protein. The triplex proteins, VP19C and VP23, are unable to associate with major capsid-scaffold protein complexes independently of one another, suggesting that VP19C and VP23 must interact with each other prior to binding to major capsid-scaffold protein subunits for capsid assembly. This indicates that the protein interactions are ordered such that the major capsid and scaffolding proteins first interact to form small subunits, as shown in Fig. 6. Heterotrimeric triplexes probably bind to these subunits, connecting them to form arc-shaped or dome-shaped partial capsids. The addition of more subunits results in formation of first a partial capsid and later a spherical procapsid, which is subsequently transformed into the mature icosahedral shell (20). While this proposed pathway is derived from observations in an in vitro system, it seems unlikely that the in vivo pathway would be unrelated.

View larger version (20K): [in this window] [in a new window]   FIG. 6.   Proposed sequence of events in the HSV-1 capsid assembly pathway, based on intermediates observed in the in vitro assembly system. The major capsid protein and the scaffold protein interact in the cytoplasm, forming VP5-pre-VP22a complexes that are localized to the nucleus (16). VP19C and VP23 interact to form triplexes, which then move to the nucleus. Assembly occurs by interaction of the two types of protein complexes, forming arc-like partial capsids that grow into a procapsid shell. Finally, the spherical procapsid matures by transformation into the icosahedral capsid. In vivo, this transformation would be expected to be accompanied by packaging of viral DNA.

In addition, immunofluorescence studies have shown that in transfected BHK cells expressing HSV capsid proteins, VP5 is transported to the nucleus through interaction with the scaffolding protein pre-VP22a (24). Another study demonstrated that VP23 is transported to the nucleus by VP19C (27), suggesting that such pairwise interactions may be required for all of the assembly components to translocate to the nucleus, where capsid assembly occurs. Studies using the two-hybrid system failed to detect direct interactions between either triplex protein and VP5 or pre-VP22a (5), further supporting the model that the triplex as a unit, rather than individual polypeptides, binds to VP5 and pre-VP22a.

Physical properties of the triplexes. Although interaction between the triplex proteins, VP19C and VP23, has previously been demonstrated by immunofluorescence (27) and in the two-hybrid system (5), sucrose density gradient analysis was useful for the physical characterization of the triplex. Gradient analysis showed that both proteins had an increased sedimentation coefficient when incubated together compared to the sedimentation coefficient for each protein when incubated alone. Therefore, VP19C and VP23 must come together to form a larger, more rapidly sedimenting protein complex. While immunoprecipitation might have been an easier method for detecting an interaction between the two proteins and determining stoichiometry, precipitating antibodies are not available for either VP23 or VP19C. However, molecular weight estimations based on the sedimentation coefficient are consistent with a heterotrimer composed of one VP19C monomer and one VP23 dimer (the expected molecular weight was 118,796; the observed molecular weight was 129,000). The protein peaks observed were not consistent with a complex composed of one VP19C monomer and one VP23 monomer, which would be predicted to have a molecular weight of 84,528, nor were the derived values consistent with a complex composed of two homodimers (expected molecular weight of 169,056). A complex containing one VP19C dimer and one VP23 monomer would have a molecular weight of 134,788, a value that is close to the calculated molecular weight of 129,000 in this experiment. However, considering the copy number for each protein, as determined by scanning transmission electron microscopy (375 for VP19C and 572 for VP23), this arrangement is unlikely to account for the majority of the triplexes (22). In addition, gradients containing only VP23 indicated that this protein exists as a dimer in solution, which supports the model of the triplex as a heterotrimer. Finally, recent studies of human cytomegalovirus triplex proteins mCP (minor capsid protein) and mC-BP (mCP-binding protein) have shown that these proteins form an mCP-BP-mCP₂ heterotrimer and that mCP (VP23 homolog) exists as a dimer when expressed alone (2). These results are consistent with our observations for HSV-1 triplex proteins.

Protein interactions. Deletion of 15 amino acids from the C terminus of VP19C resulted in a protein that was inactive in capsid assembly. Gradient analysis, however, showed that the truncated protein was still capable of interacting with VP23. Based on this result, it seems likely that the sequence at the C terminus of VP19C (451-LEGVVWRPGGWRACA-465) may be involved in specific interactions required for attachment of the triplex to the major capsid-scaffold protein complex. On the basis of the 1979 report by Zweig et al. (42) of a disulfide linkage between VP19C and VP5, it was hypothesized that the C-terminal cysteine residue might participate in a disulfide bond that links the triplex to the major capsid-scaffold protein complex. However, a single amino acid substitution changing the cysteine to an alanine (C464A) did not inhibit capsid assembly (31), suggesting that another element of the sequence may be important.

Deletion analysis of VP23. In this study deletion analysis was performed only on the VP19C triplex protein. A similar analysis performed on VP23 demonstrated that the loss of 10 residues from the C terminus or 77 amino acids from the N terminus of VP23 inhibited capsid assembly in insect cells infected with recombinant baculoviruses expressing each of the capsid proteins (12). In addition, sites of interaction with VP19C were mapped by using the two-hybrid system. These studies showed that deletion of the N-terminal 77 residues of VP23 prevents interaction with VP19C. Similarly, the loss of 71 residues from the C terminus also inhibited the interaction between the two proteins, although deletion of just 10 C-terminal residues did not. Because the two-hybrid system detects single protein interactions, it is not clear whether deletions that disrupted interaction with VP19C were due to the loss of sequences that mediate binding to VP19C or the loss of sequences that mediate the dimerization of VP23, which may be essential in order for interaction with VP19C to occur. Self-association of VP23 has not been observed in the two-hybrid system (5, 12), indicating that there are limitations to this method, particularly for the analysis of structural proteins.

Triplex structure in the capsid. In high-resolution studies of the capsid shell, Zhou et al. (41) observed that triplex structure was influenced by the local environment. Six distinct types of triplex based on the type of surrounding capsomers were described. Of particular interest are the triplexes located at the threefold axes of symmetry of each triangular face, between three central hexons. Due to symmetry imposed during reconstruction methods, the structures of these triplexes are in question. While it is interesting to speculate that a homotrimer, rather than a heterotrimer, would likely occupy these sites, no evidence for structures with that stoichiometry was observed during gradient analysis in the experiments reported here.