INTRODUCTION

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The genomes of spumaretroviruses (or foamy viruses [FV]) include the classical gag, pro-pol, and env genes that are the hallmark of the retrovirus family (9). Despite the familial relationship implied by their genome organization, FV differ from retroviruses such as oncoviruses or lentiviruses in basic aspects of replication and gene expression (30-32, 39, 53). The differences between FV and the more widely studied retroviruses, such as human immunodeficiency virus (HIV) or murine leukemia virus, provide an opportunity to identify the fundamental mechanisms of processes such as particle assembly and maturation.

The shared gene order of the FV genomes and those of other retroviruses allows the identification of common structural proteins. Unfortunately, this relationship does not extend to the structure and function of FV Gag proteins, since no obvious homologies are detectable between FV Gag and MA, CA, and NC domains of other retroviruses for which structures have been determined to high resolution (10, 43). Furthermore, the proteolytic processing of Gag that produces the familiar mature proteins in other retroviruses is unusual, incomplete, and/or delayed in FV (12, 23, 29, 37).

The available data indicate that the morphology and morphogenesis of FV are distinct from those of other retroviruses. FV Gag proteins preassemble to form in the cytoplasm spherical capsids that bud through cellular membranes (55). This process contrasts with what occurs with lentiviruses and C-type retroviruses that assemble their capsids at the site of budding but is similar to what occurs with B- and D-type retroviruses (40). Budding of human foamy virus (HFV) is strictly dependent upon the presence of Env proteins (4, 38), while budding of the other retroviruses occurs in the absence of Env. Recent results indicate that the Env leader protein (Elp) of HFV is the region that supports budding (D. Lindemann, personal communication). Electron microscopy (EM) of thin sections did not reveal the condensation of the ring-like capsids in FV particles after budding which is characteristic for the maturation of other retroviruses. Rearrangements of the FV capsids were rarely observed (34) or may not occur (14, 55). This lack of morphological maturation has been attributed to the incomplete processing of FV Gag proteins described above.

Cleavage of Gag in other retroviruses is believed to modulate its affinity for the membrane by altering the exposure of an amino-terminal acyl moiety and other motifs in MA (16, 57). The lack of complete proteolytic cleavage and the absence of basic sequence and myristylation motifs in MA that mediate membrane targeting in other retroviruses suggest that FV must bind to membranes by other mechanisms.

We combined cryoelectron microscopy (cEM) studies of HFV and feline foamy virus (FFV) particles with biosensor surface plasmon resonance (SPR) analyses of FV proteins to address the issues of Gag-membrane interaction. cEM has previously been used to demonstrate the lack of icosahedral symmetry and presence of local order in HIV and murine leukemia virus (20, 52), and it has revealed the radial arrangement of the Gag polyproteins and allowed the mapping of the positions of individual domains in HIV type 1 Gag (48, 49). In FV particles, Gag proteins are radially arranged inside the virions, and lateral interactions of Gag domains result in the formation of the MA layer and the FV capsid shell. An intimate association of the Gag MA layer and the viral membrane was detected in 20% of FFV particles. SPR technology demonstrated a direct and specific physical interaction of the FFV Elp with the N terminus of Gag. This result and the detection of the 16.5-kDa FFV Elp in released virions suggest a putative transient interaction of the MA layer and Elp during particle morphogenesis of FV.

	MATERIALS AND METHODS

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Cells and virus. Crandell feline kidney (CRFK) and HEL299 cells were grown as reported previously (50). FFV isolate FUV and the prototypic HFV were propagated as described previously (33, 50).

Purification of released FV particles. Cell culture supernatants from HFV-infected HEL299 or FFV-infected CRFK cells were harvested 4 to 6 days after infection, when the infected cells displayed strong virus-induced cytopathic effects. Cell culture supernatants were cleared by centrifugation at 400 × g for 7 min and then at 3,000 × g for 30 min (46). Supernatants were filtered through 440-nm-pore-size filters and centrifuged through 5 ml of 20% (wt/vol) sucrose in TEN (150 mM NaCl, 10 mM Tris/HCl [pH 8.0], 1 mM EDTA) for 2 h at 24,000 rpm in an SW27 rotor (Beckman, Munich, Germany). The resulting pellet was gently resuspended in phosphate-buffered saline. For further purification, the enriched particles were separated on sucrose gradients (48) or banded in a preformed 10 to 32% iodixanol (Optiprep; Nycomed Pharma, Oslo, Norway) gradient in TEN run for 16 h at 32,000 rpm in an SW41 rotor (Beckman) (3).

cEM, image analysis, and contrast transfer function correction. cEM was performed as described previously using a Philips CM200FEG operated at 200 kV at a magnification of ×38,000 (20, 49). The images were digitized on a Zeiss (Oberkochen, Germany) SCAI scanner at a step size of 14 µm. The measurements shown in Fig. 4 were performed using the SPIDER image analysis program (15). The particle diameter was measured from the outer leaflet of the membrane and thus excludes the contribution of the projection domains of the viral glycoproteins.

Expression and purification of recombinant FFV Gag and Elp. FFV Gag residues 1 to 154 were bacterially expressed in the pET16b (Novagen, Madison, Wis.) vector as described previously (5). The FFV Gag residues 1 to 154 were flanked at the N terminus by the vector-encoded His tag and 16 unrelated residues at the C terminus. Induced Escherichia coli BL21 cells were lysed in IMAC buffer in the absence of urea or other denaturing agents by sonification (5). The soluble recombinant FFV Gag 1 to 154 was purified to more than 95% homogeneity using Ni affinity chromatography, dialyzed against phosphate-buffered saline, and stored at 70°C before use. Elp residues 1 to 65 were amplified by PCR with primers 5'-GCTCATGATGGAACAAGAACATGTG-3' (the introduced BspHI site is underlined) and 5'-GGAATTCTCATCTAGTAGAAGTAGCACA-3' (the introduced EcoRI site is underlined) as described previously (55). The amplicon was digested with BspHI and EcoRI and inserted into the NcoI- and EcoRI-digested vector pET32c (Novagen). The resulting thioredoxin-Elp fusion protein of 25 kDa and the pET32c-derived thioredoxin control protein were purified to about 90% homogeneity under nondenaturing conditions by His tag affinity chromatography as described above.

Immunoblotting and induction of an Elp-specific antiserum. Immunoblotting of proteins separated on denaturing gels and detection of specifically bound antibodies by enhanced chemiluminescence and diamino-benzidine staining were done as described previously (1, 37). Synthesis of authentic and mutant Elp-derived peptides was as recently described (37). A synthetic peptide encompassing the authentic FFV Env residues 1 to 30 was directly used for immunization of guinea pigs by Eurogentec, Seraing, Belgium. The FFV MA and Env surface (SU) antisera and cat antiserum 8014 were as described previously (1, 5, 56).

Binding analysis by SPR. Protein interactions were identified and characterized by SPR technology using the BIAcore 3000 instrument (BIAcore, Freiburg, Germany) and methodology (26, 27). Coupling reagents were used according to protocols developed by the supplier.

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5

	RESULTS

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cEM of released enveloped and nonenveloped HFV particles. HFV particles released into the supernatant of infected cells were harvested and concentrated by sedimentation through sucrose. This protocol isolated enveloped HFV particles that were heterogeneous in size and shape together with some cell debris. The virions ranged in size between 55 and 250 nm and displayed a mean membrane-included diameter of 106.9 ± 8.3 nm (mean ± standard deviation) (n = 48) (Table 1). The particles were covered with spikes 15.6 ± 2.1 nm long (n = 83) that formed clusters on the virion surfaces (46). Capsid structures with diameters of 60 nm were present within the enveloped particles. The enveloped capsids were neither completely spherical nor regular but appeared angular without any apparent symmetry.

Organization of HFV particles. HFV particles purified by an additional sucrose centrifugation step (see Materials and Methods) banded at a density of approximately 1.16 g/ml, similar to that described for other retroviruses (45). Spherical HFV particles with tightly packed spikes (Fig. 1B) inserted into the viral membrane (Fig. 1A) predominated in this purified material (for a schematic presentation, see Fig. 1C and 2D). The projecting region of the spike displayed a layered appearance that was most apparent within the spike clusters, suggesting that the structural features of the Env complexes were laterally aligned in the clusters (Fig. 1B). A fraction of the particles displayed a distorted membrane and an asymmetric distribution of Env proteins and even contained two capsids as discussed below in detail for FFV.

View larger version (117K): [in this window] [in a new window]   FIG. 1.   Ultrastructure of released HFV particles (A to C) and schematic alignment of HFV and FFV Gag proteins (D). cEM of HFV reveals closely packed envelope proteins with distinct layers of density within the glycoproteins (pair of black arrows in B) covering the surface of the budded virion. A separation between the viral membrane (pair of white arrows) and the broad MA layer (white bracket and white arrowhead) is clearly visible and characteristic for budded FV particles. The MA layer width of about 8 nm is characteristic for HFV. The prominent margin of the angular HFV capsid is marked with a black arrowhead. The capsid in panel A has a central position in contrast to the off-center position of the capsid shown in panel B. The scale bar in panel B represents 50 nm. (C) Schematic presentation of structural features of HFV particles analyzed by cEM. (D) Schematic alignment of HFV and FFV Gag proteins. The presence of the C-terminal p3 cleavage site (arrow), the p3 protein, and the N-terminal, Pro-rich (P-rich), and central and C-terminal subdomains of FV Gag proteins is shown. For details, see the text.

The width of the MA layer is characteristic for different FV. Enveloped FFV particles measured 109.1 ± 11.2 nm (n = 55) in diameter and banded at a density of 1.16 g/ml. Surface staining of isolated FFV particles showed tightly packed glycoprotein complexes (data not shown) similar to those described previously for HFV (46). cEM analysis showed the spikes as projections 14 ± 2 nm (n = 103) long, with strong lateral interactions resulting in the formation of clusters as also observed in HFV. FFV particles contained an angular capsid of 63.5 ± 7.8 nm (n = 90) (Table 1 and Fig. 2D). Capsids were always separated from the viral membrane by a protein layer resembling the MA layer of HFV (Fig. 1 and 2). The thickness of the MA layer between the capsid and the viral envelope was the only consistent difference between HFV and FFV particles. Close examination of a large number of virions revealed an MA layer consistently thinner in FFV (3.8 ± 0.7 nm [n = 65]) than in HFV (8.2 ± 0.9 nm [n = 62]) (Table 1). This difference in the sizes of the MA layers may correspond to 130 additional residues in the N-terminal region of HFV compared with FFV (Fig. 1D) (42, 50).

View larger version (184K): [in this window] [in a new window]   FIG. 2.   Ultrastructure of released FFV particles (A to C) and schematic diagram of FFV particles (D). The MA layer (white arrowheads) follows the shape of the capsids in particles with central (A) and off-center (B) capsids as schematically shown in panel D. Many particles in the population show the internal angular capsid (the edge of the capsid is marked by black arrowheads) displaced from the center of the particle (B). Views in which the capsid appeared to be almost in the center of the particle were also observed (A). Occasionally, two capsids were surrounded by an almost perfect spherical viral membrane (pair of white arrows), resulting in particles with a greater diameter (B and C).

Localization of the MA layer in distinct classes of FFV particles. In 25% of the FFV particles analyzed, the isometric, angular capsid was positioned in the center of the particle (Fig. 2A). The MA layer appeared to follow the edge of the capsid, resulting in a variable distance between the MA layer and the viral membrane. That the FFV MA layer followed the shape of the capsid and was not associated with the viral membrane was more obvious when the capsid was displaced from the center of the particle (Fig. 2B). Such particles with off-center capsids represented 50% of the virus population. The ratio of central to off-center capsid locations suggests that they arise from the same particle morphology (i.e., an off-center capsid) viewed from different directions in cEM. About 5% of the particles contained two displaced capsids. In these particles, the MA layer maintained a relatively fixed distance to the body of the capsid with no obvious physical interaction with the viral membrane (Fig. 2C). In both particle types described above, the MA layer appeared to be separated from the viral membrane but was consistently localized next to the angular viral capsid as schematically shown in Fig 2D.

View larger version (220K): [in this window] [in a new window]   FIG. 3.   Features of FFV particles with a distended morphology. Particles with a distended morphology (A to D) show tight interaction of the MA layer (white arrowheads) with the viral membrane (pair of white arrows). The two opposed arrows mark the stalk of cellular membrane which is still attached to the particle (B). The pairs of black arrows mark spike proteins, and the black arrowheads point to the margin of the capsid. The scale bar in panel D represents 50 nm.

View larger version (20K): [in this window] [in a new window]   FIG. 4.   Relative localization of the MA layer in FFV particles. Arrangement of the MA layer in FFV particles with central capsids (diamonds), off-center capsids (squares), and distended morphology (triangles). The plots show the distribution of distances between the MA layer and the edge of the capsid structure (A) and between the MA layer and the inner leaflet of the viral membrane (B). The distances in nanometers are plotted against the position of the measurement on the circumference of the MA layer and were measured at 1-nm intervals. A typical result is shown for each particle type. No significant difference is seen between the mean distances from the capsid to the MA layer of the three particle types (A). In contrast, only the distended FFV particles showed a constant and close juxtaposition between the MA layer and the membrane, with a distance of 6.0 ± 0.8 nm (mean ± standard deviation) (n = 83) (B). The mean distances from the membrane to the MA layer were 8.8 ± 1.4 nm (n = 85) for central capsids and 18.3 ± 11.4 nm (n = 133) for off-center capsids.

The FFV Elp is virus associated. Recent results demonstrate that the N terminus of HFV Env is required for particle budding and that this domain is cleaved off as a protein of about 148 residues by an unknown protease (D. Lindemann, personal communication). We analyzed whether a corresponding Elp is present in FFV, since this domain may be responsible for the Gag-envelope interaction seen in cEM of distended FFV particles. FFV particles enriched by centrifugation through sucrose and FFV antigen from infected CRFK cells were subjected to immunoblotting using the FFV Env SU antiserum directed against Env residues 101 to 402 and the FFV Elp serum directed exclusively against Env residues 1 to 30 (Fig. 5). The Elp antiserum detected exclusively FFV proteins of about 16.5 kDa in virion-associated antigens, which corresponds in size to the expected FFV Elp protein (Fig. 5B, lane 4). In extracts from FFV-infected cells, the Elp antiserum specifically detected the unprocessed Env precursor of 130 kDa and the 16.5-kDa Elp (Fig. 5B, lane 2) besides an unspecific band also present in mock-infected cells (lane 3). The FFV Env SU serum detected the 16.5-kDa Elp and the 70-kDa Env SU bands in enriched FFV virions (Fig. 5A, lane 4). At the antigen concentration used, the Env SU serum did not allow detection of the FFV Elp protein in FFV-infected cells (lane 2) whereas the Env precursor and the Env SU proteins were recognized in addition to a few weak and unspecific bands.

View larger version (28K): [in this window] [in a new window]   FIG. 5.   Detection of FFV Elp in released FFV particles and FFV-infected cells. FFV particles were enriched from the cell culture supernatant from FFV-infected CRFK cells by centrifugation through sucrose as described in Materials and Methods, lysed, separated on a denaturing gel, and analyzed by immunoblotting (lanes 4). In parallel, proteins from FFV-infected (lanes 2) and mock-infected CRFK cells (lanes 3) were analyzed. The blots were reacted with the FFV SU antiserum (A) (56) and the FFV Elp antiserum (B) and specific proteins were detected by diamino-benzidine staining (A) and enhanced chemiluminescence (B). The positions of Elp, Env-SU, and the gp130Env precursor are marked. Two different prestained molecular mass markers were used in lanes 1. The gel in panel A contained 16% polyacrylamide, and that in panel B contained 14% polyacrylamide.

View larger version (35K): [in this window] [in a new window]   FIG. 6.   Cosedimentation of FFV Elp with FFV particles. FFV particles enriched by centrifugation through 20% sucrose were analyzed on preformed 10 to 32% iodixanol gradients as described in Materials and Methods. Regular aliquots of the gradient fractions (as indicated) were directly analyzed by immunoblotting using the FFV-specific cat antiserum 8014 (A) and the FFV Elp antiserum (B). Proteins were detected by enhanced chemiluminescence. The positions of the p52 and p48 Gag and the FFV Elp proteins are marked. In lanes M, prestained molecular mass markers were separated in parallel.

Specific interaction of the N-terminal domains of FFV Gag and Elp determined by SPR. The close association between the MA layer and Env-bearing membrane regions described above for distended FFV particles may reflect a specific interaction between defined regions in Gag and Env. We used SPR to identify and characterize putative interactions between a portion of the N-terminal FFV Elp and the N-terminal region of the Gag polyprotein.

View larger version (13K): [in this window] [in a new window]   FIG. 7.   Interaction of FFV Elp-derived peptides with FFV Gag 1-154. SPR analysis of the binding of FFV Elp-derived peptides to the recombinant N-terminal FFV Gag 1-154 domain bound to the sensor surface. Each peptide solution (50 µg/ml) was passed over the FFV Gag sensor surface at a flow rate of 10 µl/min for 3 min. The peptide representing the wt FFV (Elp residues 1 to 30) is designated WW, AW represents the single W12A, WA represents the W15A exchange, and both Trp residues have been replaced by Ala in peptide AA. A human collagen-derived peptide (unrelated peptide) served as an additional control. The signals for binding were automatically recorded after the binding reaction reached equilibrium and are presented as relative response units.

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View larger version (39K): [in this window] [in a new window]   FIG. 8.   (A) Kinetic analyses of the interaction of the authentic Elp-derived peptide with FFV Gag 1-154 coupled to the CM5 sensor. The peptide WW was passed over the sensor chip at a flow rate of 10 µl/min for 2.5 min at concentrations ranging from 2.08 × 107 to 1.33 × 105 M as shown in the inset. The fast associations and dissociations are graphically expressed as relative response over time in minutes. Regeneration of the sensor surface was complete and achieved by changing to HBS buffer. Arrow, start of the binding reaction; asterisk, beginning of the washing with HBS buffer. (B) Kinetic analyses of the interaction of the FFV MA antiserum with FFV Gag 1-154 coupled to the CM5 sensor. Defined dilutions of the FFV MA antisera ranging from 1:500 to 1:8,000 were passed over the sensor chip at a flow rate of 10 µl/min for 2.5 min corresponding to immunoglobulin G concentrations from 14 to 0.88 µg/ml as shown in the inset. The slow association of the polyclonal antiserum at concentrations reaching saturation and the very low dissociation of the bound antibodies are graphically expressed as relative response over time in minutes. (C) Kinetic analyses of the interaction of the FFV Gag 1-154 protein coupled to the CM5 sensor with the purified thioredoxin-Elp 1-65 fusion protein. Defined concentrations of the recombinant thioredoxin-Elp 1-65 fusion protein ranging from 62 to 15.5 µg/ml were passed over the sensor chip at a flow of 15 µl/min for 3 min. The slow and specific association of the thioredoxin-Elp 1-65 and the slow dissociation of the bound Elp protein are graphically expressed as relative response over time in minutes. The thioredoxin protein without the FFV Elp domain did not show any specific binding. Arrow, start of the binding reaction; asterisk, beginning of the washing with HBS buffer.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

We have used cEM of FFV and HFV to address the relationship of FV structure to that of better characterized retroviruses such as B, C, and D types and lentiviruses. FV share the heterogeneous size of released retroviral particles, the lack of icosahedral symmetry, and the radial arrangement of defined Gag domains with the other retroviruses that have been examined (20, 47, 49, 52).

Comparative cEM of HFV and FFV revealed the FV MA layer, a novel structural feature which was not visible in EM of thin sections. In analogy to other retroviruses, the FV MA layer is considered to consist primarily of the N-terminal Gag domain. This assumption is supported by the difference in the sizes of the HFV and FFV MA layers, a difference which likely corresponds to 130 additional residues in the N-terminal region of HFV compared with FFV (Fig. 1D). In contrast, the central and C-terminal Gag domains of the known FV are similar in size (Fig. 1D) (42, 50), corresponding to the almost identical dimensions of FFV and HFV capsids (Table 1). It is assumed that the central and C-terminal regions of FV Gag are primarily involved in capsid formation and genome binding (54). The size and shape of the FV capsid structures do not match those of the hepadnaviruses despite their functional similarities with retroviruses and FV (2).

The second feature that distinguishes FV particles from those of other retroviruses is the fact that the N-terminal domain of the Env precursor Elp, about 16.5 kDa in size, is a virion-associated protein. A similar observation has been previously reported for HFV (D. Lindemann, personal communication), whereas the much smaller N-terminal signal peptides of other retroviruses are not part of the virion (24).

Whereas the function of the classical signal peptide is considered to be the targeting of Env into the lumen of the endoplasmatic reticulum (24), the FV Elp appears to have additional functions. Our present biosensor SPR work reveals a specific interaction of the N-terminal sequences of the Elp with the N-terminal region of the FFV Gag protein in vitro. Two conserved Trp residues in Elp were required for binding. Corresponding interactions have not been shown for any other retrovirus. The data obtained with the substitutions of Ala for Trp in the FFV Elp peptides complement the results of genetic experiments on HFV budding with the same amino acid substitutions (D. Lindemann, personal communication).

The on and off rates and affinities observed in the SPR studies with the Elp peptides and the recombinant N-terminal Elp domain are expected to yield specific and possibly even reversible interactions (25, 41). Virus morphogenesis and the formation of other higher-order protein complexes rely upon concerted effects of many specific interactions. These generate the metastable protein assemblies that support the efficient disassembly that is required for infection (7).

The secondary structure of the Elp peptide is predicted by the computer program DSC for discrimination of protein secondary structure classes (28) to be identical to that in the full-length Env. The part of Elp which had been altered in the mutant peptides is predicted to form a stable helix even when both Trp residues have been replaced with Ala. Due to this intrinsic stability of the secondary structure, the Elp peptides used for the assays may adopt a conformation comparable to that in the viral particle. The significantly stronger binding of Elp residues 1 to 65 in the context of the fusion protein compared to the 30-mer Elp WW peptide indicates that flanking residues and/or the overall folding of the cytoplasmic domain of Elp are important for binding. By analogy, Elp-Gag binding may be further modulated by the conformation and/or processing of the Gag and Env precursor molecules.

Our data indicate that the N-terminal domain of Elp has an intrinsic morphogenetic function in directing specific Env-MA interactions. Such a function would require that the N terminus of Elp be located at the cytoplasmic side of those membranes where FV budding takes place. Consistently, subtilisin digests of purified FFV particles actually showed that the N terminus of Elp is located inside the particle (data not shown). Thus, the direct interaction of FV Elp with Gag may subsume the role played by the membrane binding subdomain of other retrovirus MA proteins. Detailed studies of the HIV-1 MA domain in the context of the Gag precursor have shown that binding of MA to membranes involves at least several domains of the MA protein (17).

The Elp-Gag interaction appears to be unique to FV, since heterologous leader peptides in other retroviruses support the formation of infectious particles. It is conceivable that the specificity of the FV Elp-Gag interactions is the reason for the inability to pseudotype HFV particles (38). Evidence for Env-Gag interactions has been previously reported for other retroviruses; however, the interactions involve the C-terminally located cytoplasmic tail of Env rather than the leader peptide (17, 35, 44, 51).

Morphological evidence for an Env-Gag interaction was obtained only in the FFV particles with distended morphology (Fig. 3 and Table 2). The morphology of these particles clearly resembled that of the budding forms of other retroviruses including FV (4, 6, 21, 22, 36, 38, 55). The envelope of the distended particles was incompletely closed, and the particles were composed of a spherical portion and a protruding tail (Fig. 3). We interpret them as FFV budding intermediates that coisolated with the properly budded spherical FFV particles. An alternative explanation that they represent disrupted particles or fusion intermediates cannot be ruled out. Nevertheless, the distended forms reveal structural features that may be present transiently during morphogenesis even if these particles are dead-end or abortive assemblies.

Provided that the distended FFV particles represent budding intermediates, the Elp-MA layer interaction could serve the morphogenetic role of targeting preformed FV capsids to the membrane and/or concentrating Env trimers at the site of budding. The FV Elp-MA interaction may interfere with the cytoplasmic Gag targeting and retention of preassembled capsids. Such targeting and retention have been shown to exist for Mason-Pfizer monkey virus Gag and are probably mediated by the interaction of MA sequences with cellular proteins (8). In other retroviruses, membrane targeting and binding are attributed to the MA shell located directly under the viral membrane (17). In FV, lateral Env-Env interactions seen in cEM (Fig. 1 to 3) may provide the driving force that leads to budding of FV particles, explaining the Env dependency of this process in FV (4, 38). After budding is completed, the FV MA layer should need to dissociate from the viral membrane as it remains covalently linked to the capsid. This process may be modulated by proteolysis, which would implicate that the mature Elp may have functions different from those in the uncleaved Env precursor. Additional experiments are required to determine the function of the Elp-Gag interactions during morphogenesis and maturation.

In summary, the combination of cEM, immunoblotting, and SPR allowed us to determine the structural features of FV particles, to identify the virion-associated FFV Elp protein, and to characterize the molecular basis of the FV Gag-Env interactions.