INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

The production of lentivirus particles from infected cells involves multiple steps, including viral protein transport to and association with the plasma membrane, assembly of the structural proteins, encapsidation of the genomic RNA, and particle release (for reviews, see references 11 and 49). The Gag polyprotein precursor plays a central role in these events and, in fact, is both necessary and sufficient for the assembly and release of immature viruslike particles (VLPs). The human immunodeficiency virus type 1 (HIV-1) Gag precursor, Pr55^Gag, is composed of four major domains: matrix (MA or p17), capsid (CA or p24), nucleocapsid (NC or p7), and p6. Two spacer peptides are also present within Pr55^Gag: p2, located between CA and NC, and p1, located between NC and p6. Pr55^Gag is cleaved by the viral protease (PR) during or immediately after virus budding from the cell to produce the mature Gag proteins.

The primary determinants of Gag membrane binding appear to lie within MA. This domain contains a signal for N-terminal myristylation, and it is well established that the covalent modification of Gag with myristic acid is essential for efficient membrane binding of Pr55^Gag (11). Accumulating evidence suggests that not only the presence but also the degree of exposure of this fatty acid is important for Gag membrane binding and that the latter may be controlled by the conformation of MA. This hypothesis, referred to as the myristyl switch model, originally derived from studies involving cellular proteins (e.g., recoverin) that bind membrane in a reversible manner (3, 34). The myristyl switch model has been applied to HIV-1 Gag to explain the observation that membrane binding of mature p17(MA) is much weaker than that of Pr55^Gag. According to this model, the myristate moiety is highly exposed in the context of Pr55^Gag but is sequestered within p17(MA) following proteolytic cleavage of the precursor by PR (21, 48, 63). We have shown that single amino acid substitutions in MA can increase or decrease membrane binding of Pr55^Gag in a manner dependent on myristylation, perhaps by changing the degree of myristate exposure (37).

Although the myristic acid moiety attached to the N terminus of the MA domain is clearly critical for Gag membrane binding, thermodynamic considerations suggest that the myristate alone cannot provide sufficient binding energy to anchor Pr55^Gag at the lipid bilayer (41). It therefore seems likely that domains elsewhere in the protein contribute to Gag membrane binding. Indeed, structural (22, 32) and biochemical (62) data have implicated a highly basic domain spanning MA amino acids 17 to 31 in membrane binding. However, seemingly contradictory results have been reported from deletion mutagenesis studies in which Gag proteins lacking most or all of MA are able to efficiently produce virus particles (29, 46, 53, 55). We recently reported that mutations in the MA basic domain influence both membrane binding and the targeting of Gag to the plasma membrane and that the roles of MA in membrane binding and Gag targeting are genetically separable (38).

Multiple domains in Pr55^Gag have been proposed to mediate Gag multimerization. Based on X-ray crystallography studies, both HIV-1 and simian immunodeficiency virus (SIV) MA were reported to form trimers (22, 44), and biochemical assays utilizing MA expressed in bacteria or in a baculovirus system also suggested the ability of MA to trimerize (35, 36). Although mutations that disrupted MA trimerization impaired virus particle assembly in a baculovirus overexpression system (36), the biological relevance of MA trimerization in virus replication remains in question since, as mentioned above, deletion mutants lacking most or all of MA are able to efficiently assemble and release virus particles. A number of studies utilizing various expression systems have suggested a role for Gag domains spanning CA, p2, and NC in virus assembly (for a review, see reference 11). However, the relative contribution of each of these domains in promoting Gag-Gag interactions is unclear. Bacterially expressed CA has been shown to assemble in vitro (10, 20, 51), and the C-terminal domain of CA dimerizes in the crystal structure in the absence of other domains (16). Mutations affecting the C-terminal domain of HIV-1 CA have also been shown to disrupt virus assembly (8, 26, 45, 50, 54, 59). In contrast, mutations in the N-terminal domain of CA generally do not disrupt virus assembly but rather perturb proper virion maturation (45, 52). In some reports, the p2 spacer peptide was observed to play a major role in VLP assembly (1, 25, 28, 35, 53), although another study observed a role for p2 in virion morphogenesis but not in Gag assembly itself (42). It has been proposed that basic domains in NC are essential for retroviral Gag-Gag interaction (4-6), and data from several groups have suggested that HIV-1 NC promotes efficient virus particle assembly (7, 9, 17, 23, 53, 60, 61). In some cases, however, NC appears to be dispensable for efficient VLP assembly and release (25, 35). The latter studies were performed using a high-level baculovirus overexpression system in which Gag concentrations are likely to substantially exceed physiological levels.

In addition to its proposed role in promoting Gag-Gag interactions, it has also been reported that NC is critical for high-level binding of Gag to membrane (43, 47). Together with the reports implicating NC in Gag multimerization, these findings suggested the possibility that Gag multimerization is a prerequisite for efficient membrane binding.

In this study, we examine the relationship between Gag multimerization and membrane binding by analyzing C-terminally truncated Gag proteins for their ability to form VLPs when singly expressed, to copackage into VLPs when coexpressed with full-length Gag, and to bind membrane. Since some of the discrepancies in previous studies regarding the mapping of Gag multimerization domains likely resulted from the use of different expression systems, we expressed the Gag mutants under relatively physiological conditions, i.e., in human (HeLa) cells in the context of HIV-1 proviral clones. We demonstrate, in vivo, that strong interactions between Gag proteins are promoted by multiple determinants within the C-terminal region of CA, p2, and the N-terminal region of NC. Significantly, we observe that a truncated Gag protein lacking these sequences, and containing only MA and the N-terminal domain of CA, binds membrane at levels comparable to those of full-length Pr55^Gag. These results indicate that neither NC nor other strong Gag multimerization domains are required for efficient binding of HIV-1 Gag to membrane.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Cell culture and transfection. HeLa cells were maintained as previously described (12). Transfection of HeLa cells was performed by the calcium phosphate precipitation method as reported before (13).

Plasmids, mutagenesis, and DNA cloning. Construction of the derivative of the HIV-1 proviral molecular clone pNL4-3 (2) containing a GlyAla change at MA amino acid 1 (the 1GA mutant) has been reported previously (13). The pNL4-3/PR molecular clone, which contains a PR active-site mutation (AspAsn change at PR amino acid 25), has been described previously (24). The pNL4-3 derivatives pNL4-3/p41stop and pNL4-3/MAstop, which contain stop codons in the sequences encoding p2 amino acid 1 and CA amino acids 1 and 2, respectively, have been described previously (37). Construction of the double mutants pNL4-3/1GA/MAstop, pNL4-3/1GA/p41stop, and pNL4-3/1GA/PR has been detailed previously (37).

VLP incorporation assay and Western blotting. HeLa cells were cotransfected with pNL4-3 derivatives expressing truncated Gag proteins and pNL4-3/PR (expressing full-length Pr55^Gag) at a DNA ratio of 1:1. Two days posttransfection, virions were pelleted from culture supernatants; VLP and cell lysates were prepared as detailed previously (12, 57). Cell and VLP lysates were analyzed by Western blotting essentially as previously described (27). Gag proteins were detected with a mixture of three mouse monoclonal antibodies against MA (from Advanced Biotechnologies, Columbia, Md.; Cellular Products, Buffalo, N.Y.; and Capricorn, Scarborough, Maine) as primary antibodies and horseradish peroxidase-conjugated anti-mouse immunoglobulin (Ig; Amersham) as a secondary antibody. Detection was performed with enhanced chemiluminescence Western blotting reagents (Amersham). To avoid overexposure of blots of cell-associated material, eightfold less lysate was loaded for cell- than for VLP-associated material. For quantification of Gag proteins, alkaline phosphatase-conjugated anti-mouse Ig (Amersham) was used as a secondary antibody; detection with enhanced chemifluorescence Western blotting reagents (Amersham) was performed in accordance with the manufacturer's instructions using a Fuji FLA-2000 image analyzer.

Confocal microscopy. The methods used to examine transfected HeLa cells by confocal microscopy have been described recently (38). Briefly, HeLa cells were cultured in chamber slides (Nunc) and transfected by the calcium phosphate precipitation method without glycerol shock. Two days posttransfection, cells were fixed with 3.7% formaldehyde, permeabilized with phosphate-buffered saline (PBS) containing 0.1% Triton X-100, and incubated with anti-p17 monoclonal antibody (Cellular Products, Inc.) and Texas red-conjugated anti-mouse IgG. Cells were mounted with Fluoromount G (Virotech International) and examined with a Zeiss LSM410 laser scanning microscope.

Analysis of VLP density. VLPs were pelleted from the culture supernatant of transfected HeLa cells and resuspended in 0.4 ml of PBS. Resuspended VLPs were placed onto a sucrose gradient composed of 20, 30, 40, 50, and 60% sucrose layers in PBS (0.95 ml each). The gradients were centrifuged at 100,000 × g for 16 h at 4°C in a Beckman SW55Ti rotor. Eleven fractions were collected from the top of the centrifuge tubes. Fractionated samples were analyzed as described above.

Membrane-binding assay. Membrane flotation centrifugation was performed as detailed previously (37, 38). Briefly, HeLa cells were collected in PBS, washed once with 10 mM Tris-HCl (pH 7.5) containing 1 mM EDTA and 1 mM EGTA, and resuspended in 10 mM Tris-HCl containing 1 mM EDTA, 6% (wt/vol) sucrose, and Complete protease inhibitor cocktail (Boehringer Mannheim). Postnuclear supernatants obtained after sonication of cell suspensions were mixed with 85.5% (wt/vol) sucrose and placed on the bottom of a centrifuge tube. On top of this postnuclear supernatant-containing 73% (wt/vol) sucrose mixture was layered 65 and 10% (wt/vol) sucrose. The gradients were centrifuged at 100,000 × g for 18 h. Ten fractions were collected from the top of the centrifuge tube. Fractionated samples were analyzed by Western blotting as previously described (27). Quantitation of Western blotting data was performed by densitometry scanning. Similar results were obtained when Pr55^Gag-expressing cells were disrupted by homogenization rather than sonication (unpublished results).

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Construction of HIV-1 Gag truncation mutants. To examine the relationship between Gag-Gag interaction and membrane binding, we constructed a series of C-terminal Gag truncation mutants (Fig. 1). To minimize the disruption of native Gag conformation, stop codons were introduced either immediately following Pr55^Gag cleavage sites or adjacent to known structural domains. The NC35stop mutant is truncated just before the second NC zinc finger and thus includes the two highly basic domains of NC (located at the NC N terminus and between the two zinc finger motifs). The p43stop mutant is truncated immediately after the p2/NC cleavage site to produce an MA-CA-p2 Gag protein. p41stop contains all of MA and CA, while CA146stop is truncated at CA amino acid 146 (in the linker region between the N- and C-terminal domains of CA [15, 58]) and therefore contains MA and the N-terminal domain of CA. The MAstop mutant expresses only p17(MA). These mutations were introduced into the HIV-1 molecular clone pNL4-3 (2). All Gag proteins were synthesized in the absence of PR; to express full-length Pr55^Gag, we used a PR version of pNL4-3, pNL4-3/PR (24). The truncated clones were also PR, since the stop codons in Gag prevented the synthesis of Pr160^Gag-Pol.

View larger version (16K): [in this window] [in a new window]   FIG. 1.   Schematic representation of HIV-1 Gag C-terminal truncation mutants. The domain structure of the Gag precursor Pr55Gag is shown at the top. The regions expressed in the truncation mutants analyzed in this study are indicated. The two heavy lines over CA represent the two structural domains of this protein. The zinc finger motifs (Zn) of NC are represented by stippled boxes.

Sequences within the NC domain of HIV-1 Gag are essential for efficient VLP assembly. We first tested the ability of the Gag truncation mutants to form VLPs. HeLa cells were transfected with pNL4-3/PR or pNL4-3 derivatives expressing the Gag truncation mutants. Cell and VLP lysates prepared 2 days posttransfection were analyzed by Western blotting with a mixture of monoclonal antibodies against MA (Fig. 2). Approximately 28% of the total amount of full-length Gag expressed was VLP associated. Relative to full-length Gag, pNL4-3/NC35stop-transfected cells produced a reduced but readily detectable amount (12%) of VLP-associated Gag protein. Approximately 2% of p43 Gag was recovered in the medium in a pelletable form. Less than 1% of p41 and CA146 Gag proteins were found in the pelleted medium. We observed a low level (approximately 2%) of pelletable material released into the medium of cells expressing MA alone (MAstop). These results are in agreement with studies (7, 9, 60) suggesting that domains within HIV-1 NC play an important role in VLP assembly and release.

View larger version (40K): [in this window] [in a new window]   FIG. 2.   VLP production of singly expressed truncation mutants. (A) HeLa cells were transfected with pNL4-3/PR or pNL4-3 derivatives expressing the indicated truncated Gag proteins. VLPs were pelleted from the supernatant of transfected cells by ultracentrifugation. Cell-associated (assoc., left panel) and VLP-associated (middle and right panels) material was analyzed by Western blotting with a mixture of three monoclonal antibodies against MA. As a percentage of total material recovered, eightfold more VLP-associated than cell-associated material was loaded onto the gels. The rightmost panel shows a longer exposure (exp.) (12-fold) of the middle panel. The positions of the full-length Gag precursor Pr55Gag, NC35, p43, p41, CA146, and MA proteins are shown. The positions of molecular size markers are indicated at the right (in kilodaltons). (B) Percentage of total Gag expressed that is released from the cell in a pelletable form. Data represent averages of three experiments; standard deviations are indicated by error bars.

Gag multimerization is promoted by the C-terminal domain of CA and by p2 and NC. To analyze Gag-Gag interaction further, we next assessed the ability of the truncated Gag mutants to be assembled into VLPs when coexpressed with full-length Gag. HeLa cells were transfected with a 1:1 ratio of pNL4-3/PR and pNL4-3 derivatives expressing the truncated Gags. Cell and VLP lysates were analyzed by Western blotting using a mixture of monoclonal antibodies against MA (Fig. 3). Release of VLP-associated Pr55^Gag was not affected by coexpression of any of the truncated Gag proteins, indicating that, at least at a 1:1 DNA ratio, the truncated Gag molecules did not transdominantly interfere with wild-type assembly and release. When NC35, p43, and p41 were coexpressed with full-length Gag, approximately 27, 21, and 12%, respectively, of the total amount of truncated Gag expressed was incorporated into VLPs. In contrast, only a very small amount of CA146 and MA were VLP associated (approximately 3 and 4%, respectively). Consistent with data obtained using similar constructs in an in vitro binding assay (6), these results suggest that the CA146 and MA proteins lack domains involved in promoting strong Gag-Gag interactions in vivo.

View larger version (33K): [in this window] [in a new window]   FIG. 3.   Coexpression of full-length Gag with the myristylated (WT) forms of the truncated Gag proteins. (A) HeLa cells were singly transfected with pNL4-3/PR (lanes -) or cotransfected with pNL4-3/PR and pNL4-3 derivatives expressing the indicated truncated Gag proteins. Cell- (left panel) and VLP- (right panel) associated material was analyzed as described in the legend to Fig. 2. The positions of the full-length Gag precursor Pr55Gag, NC35, p43, p41, CA146, and MA proteins are shown. (B) Percentage of total truncated Gag expressed that is released from the cell in a pelletable form. Data represent averages of three experiments; standard deviations are indicated by error bars.

View larger version (54K): [in this window] [in a new window]   FIG. 4.   VLP density analysis. HeLa cells were singly transfected with pNL4-3/PR (top panel) or pNL4-3/p41stop (second panel) or cotransfected with both pNL4-3/PR and pNL4-3/p41stop (bottom panel). VLPs recovered from the transfected cell supernatants were loaded onto 20 to 60% sucrose gradients. In the third panel, VLPs derived from pNL4-3/PR-transfected cells were mixed with those from a fourfold-greater number of pNL4-3/p41stop-transfected cells before sucrose gradient centrifugation. The second and third panels were intentionally overexposed to allow visualization of the low-level p41 VLP-associated material. Gag proteins were detected as described in the legend to Fig. 2. Pr55Gag and p41 are shown.

View larger version (33K): [in this window] [in a new window]   FIG. 5.   Coexpression of full-length Gag with nonmyristylated (1GA) forms of the truncated Gag proteins. (A) HeLa cells were singly transfected with pNL4-3/PR (lanes -) or cotransfected with pNL4-3/PR and pNL4-3 derivatives expressing the indicated truncated Gag proteins. Cell- (left panel) and VLP- (right panel) associated material was analyzed as described in the legend to Fig. 2. The positions of the full-length Gag precursor Pr55Gag, NC35, p43, p41, CA146, and MA proteins are shown. (B) Percentage of total truncated Gag expressed that is released from the cell in a pelletable form. Data represent averages of three experiments; standard deviations are indicated by error bars.

View larger version (113K): [in this window] [in a new window]   FIG. 6.   Confocal microscopy of Gag-expressing cells. HeLa cells were transfected with pNL4-3/PR (A), pNL4-3/1GA/PR (B), pNL4-3/1GA/NC35stop (C), or pNL4-3/1GA/CA146stop (D) and examined by confocal microscopy as described in Materials and Methods.

Strong Gag-Gag interaction domains are not necessary for efficient binding of HIV-1 Gag to membrane. To examine the relationship between Gag-Gag interaction and membrane binding, we next measured the ability of the truncated Gag proteins to bind membrane. We performed membrane flotation centrifugation (Fig. 7), which we and others have previously used to analyze steady-state HIV-1 Gag membrane binding (37, 39, 48). This method can distinguish oligomeric, non-membrane-bound Gag complexes from membrane-bound Gag, a separation that cannot be achieved by conventional subcellular fractionation techniques. In a previous study, we used this approach to confirm that MA binds membrane much less efficiently than does full-length Gag and to demonstrate that mutations near the N terminus of MA impair Gag membrane binding without affecting the addition of myristate (37). HeLa cells were transfected with pNL4-3/PR or pNL4-3 derivatives expressing the C-terminal Gag truncation mutants. Postnuclear supernatants of cell homogenates were subjected to membrane flotation centrifugation, followed by Western blotting analysis of the fractions derived from the centrifugation (Materials and Methods). Fractions 3 and 4 contain membrane-bound material; non-membrane-bound proteins are recovered in fractions 9 and 10 (37) (see Materials and Methods). Consistent with previous data obtained in HeLa cells (37, 39) approximately 40% of full-length Pr55^Gag was recovered in the membrane-containing fractions (Fig. 7), whereas approximately 3% of MA floated to fractions 3 and 4. NC35, p43, and p41 showed approximately 75, 50, and 25% membrane binding, respectively. Interestingly, CA146 was recovered in membrane fractions to the same extent as full-length Pr55^Gag (approximately 40%). These results, together with the data presented in Fig. 2, 3, and 5, indicate that strong Gag-Gag interaction domains are not required for HIV-1 Gag to achieve a high level of membrane binding.

View larger version (58K): [in this window] [in a new window]   FIG. 7.   Effects of C-terminal truncation on Gag membrane (memb.) binding. HeLa cells were transfected with pNL4-3/PR (Pr55Gag) or its derivatives expressing the indicated truncated Gag proteins. Postnuclear supernatants were prepared and subjected to equilibrium flotation centrifugation (Materials and Methods), during which membrane-bound material floated to the interface between 10 and 65% sucrose (fractions 3 and 4). Gag proteins were detected as described in the legend to Fig. 2.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

In this study, we demonstrate that the region of HIV-1 Gag spanning the C-terminal domain of CA, p2, and the N-terminal 35 amino acids of NC promotes strong Gag-Gag interaction (Fig. 2, 3, and 5). Extension of Gag from amino acid 146 of CA (CA146) to residue 35 of NC (NC35) incrementally increases truncated Gag incorporation into VLPs through interaction with full-length Pr55^Gag. It is therefore likely that multiple sequences act cooperatively to promote Gag multimerization during assembly, either by contributing directly to Gag-Gag interaction or by influencing the conformation of interacting sequences. Although truncations that remove the C-terminal domain of CA and downstream sequences block the ability of truncated molecules to interact with full-length Pr55^Gag and become packaged into VLPs, a truncated version of Gag containing only MA and the N-terminal domain of CA (CA146) is capable of high-level membrane binding (Fig. 7). These results indicate that strong Gag-Gag interaction domains are not required for efficient binding of Gag to membrane.

It is well established that MA binds membrane quite weakly relative to full-length Pr55^Gag (21, 37, 48, 63). It has been proposed that after Pr55^Gag cleavage, MA undergoes a conformational transition that results in the sequestration of the N-terminal myristate moiety and a reduction in membrane-binding potential (see Introduction). The difference between MA and CA146 in membrane-binding ability can also be explained by this conformational switch model: the addition of the N-terminal domain of CA to MA may induce a conformational change in the MA domain that exposes membrane-binding determinants, including the N-terminal myristate. We consider it unlikely that the N-terminal domain of CA itself functions directly in promoting membrane binding, since cryoelectron microscopy of immature HIV-1 particles suggests that Gag sequences C-terminal to MA are oriented away from the membrane in a rod-like fashion (14). The hypothesis that efficient membrane binding of CA146 is highly dependent on its conformation is supported by our observation that the addition of a short polypeptide sequence (the FLAG epitope tag) to the C terminus of CA146 significantly reduces its membrane-binding ability (A. Ono and E. O. Freed, unpublished data). In an attempt to define further the amount of CA sequence necessary to obtain high-level membrane binding, we constructed Gag truncation mutants which terminated at CA residue 14 (CA14) or 93 (CA93). However, poor detection or instability of these truncated molecules hampered our efforts to definitively determine their membrane-binding properties (unpublished data).

Although the MA and CA146 Gag proteins are unable to coassemble with full-length Gag into VLPs, we cannot exclude the possibility that they may retain some ability to form low-order multimers. It has been reported that p17(MA) as well as p41 (MA-CA) Gag proteins can form trimers in a baculovirus overexpression system (35), and SIV MA is reportedly capable of forming VLPs (18, 19). HIV-1 MA has also been observed by some (56) but not by others (18) to form low-density particles. We find a low level of pelletable material produced by expression of MA. Nevertheless, it is clear that the determinants for strong Gag-Gag interaction (as defined by the ability to promote copackaging with full-length Gag in VLPs) are located downstream of the sequences present in CA146. Consistent with these results, Gag molecules truncated after MA or between the N- and C-terminal domains of CA did not interact with full-length Gag in an in vitro multimerization assay (6), and a truncated Gag molecule (p41) lacking NC was unable to form high-molecular-weight, detergent-resistant complexes in Gag-expressing cells (30). We also observed that 1GA/NC35 was recruited into membrane fractions much more efficiently than 1GA/MA or 1GA/CA146 when coexpressed with full-length Pr55^Gag (Ono and Freed, unpublished data). This intracellular interaction assay confirms the data obtained with the VLP incorporation studies and supports the conclusion that the region of Gag spanning the C terminus of CA to the N terminus of NC promotes strong Gag-Gag interactions.

The inability of myristylated or nonmyristylated MA and CA146 to become incorporated into VLPs upon coexpression with full-length Gag does not appear to be due to differential subcellular localization of the truncated and full-length molecules. Examination by confocal microscopy of cells expressing 1GA/NC35 (which is readily incorporated into VLPs) and 1GA/CA146 (which is not efficiently incorporated) revealed no differences in subcellular localization (Fig. 6). In addition, several lines of evidence suggest that Gag multimerization may occur efficiently between two Gag molecules which, when expressed alone, are differentially targeted. (i) As demonstrated here and previously (6), nonmyristylated HIV-1 Gag readily interacts with myristylated Gag and becomes packaged into VLPs despite the fact that the nonmyristylated protein displays a diffuse, cytoplasmic localization pattern, whereas the myristylated protein shows a punctate, largely plasma membrane-associated distribution (Fig. 6) (38). (ii) We recently demonstrated that mutant Gags that are retargeted to the Golgi as a result of substitutions in MA are efficiently rescued into VLPs when coexpressed with the wild type (38). (iii) A study of the incorporation of HIV-1 Gag--galactosidase fusion proteins into VLPs indicated that the ability of various truncated molecules to become incorporated did not correlate with their patterns of subcellular localization (54). Together, these results suggest that Gag-Gag interactions may take place early after synthesis before sorting to different subcellular compartments takes place.

It is noteworthy that incorporation of truncated Gag proteins, especially NC35, p43, and p41, into VLPs is higher for myristylated than for nonmyristylated forms of the truncated molecules (Fig. 3 and 5). This observation suggests that membrane binding may facilitate Gag-Gag interaction by concentrating Gag molecules on the cytoplasmic surface of the plasma membrane. Thus, although membrane binding is clearly not required for Gag multimerization to occur (Fig. 5) (6, 31), it may enhance the efficiency of Gag-Gag interaction. The higher levels of VLP-associated Gag observed with myristylated forms may also reflect the passive incorporation of molecules solely due to their presence on the plasma membrane where virus particle formation occurs.

It has been reported that sequences in the HIV-1 NC known to promote Gag-Gag interaction (6, 7; this study) are required for HIV-1 Gag to bind membrane at levels observed for full-length Pr55^Gag (43, 47). These results led to the proposal that NC is essential for efficient membrane binding or for the stable retention of Gag at the membrane (43, 47). However, our finding that the CA146 Gag protein, which lacks NC sequences, was recovered in membrane fractions to the same extent as full-length Pr55^Gag (Fig. 7) clearly indicates that strong Gag-Gag interactions promoted by NC are not necessary for Gag to achieve a high level of membrane binding. The discrepancy between these results in terms of a requirement for NC in Gag membrane binding can be explained by two major differences in the studies: (i) a Gag truncation mutant analogous to CA146stop was not analyzed in the studies that observed a low membrane-binding ability of Gag molecules lacking NC sequences (43, 47), and (ii) we used membrane flotation centrifugation instead of traditional fractionation techniques to measure membrane binding. As we have demonstrated previously (37), membrane flotation centrifugation can separate membrane-bound material from non-membrane-bound Gag complexes, whereas standard fractionation techniques fail to achieve this separation. Since NC promotes the formation of Gag complexes, it increases the amount of pelletable Gag in fractionation assays. While CA146 binds membrane at levels comparable to those of Pr55^Gag, the increased membrane-binding ability of p43 versus p41 and NC35 versus p43 (Fig. 7) suggests that Gag multimerization may enhance membrane-binding potential to some extent.

During the course of HIV-1 replication, Gag membrane binding and virus assembly are driven not by the mature Gag proteins but by the Pr55^Gag precursor. Thus, information relating to the structure of the MA domain of Pr55^Gag would be highly informative for the understanding of the late stages of the virus replication cycle. At this time, the structure of only the mature, nonmyristylated MA protein is available (22, 32, 33, 44). Because of its large size, attempts to obtain nuclear magnetic resonance spectroscopy or X-ray crystallography data with full-length Pr55^Gag would be a technically daunting task. However, since it binds membrane at levels comparable to full-length Pr55^Gag, the myristylated CA146 protein may prove useful in solving the structure of the membrane-binding-competent form of HIV-1 MA.