- Open Access
Characterization of the invariable residue 51 mutations of human immunodeficiency virus type 1 capsid protein on in vitro CA assembly and infectivity
© Abdurahman et al; licensee BioMed Central Ltd. 2007
- Received: 10 August 2007
- Accepted: 28 September 2007
- Published: 28 September 2007
The mature HIV-1 conical core formation proceeds through highly regulated protease cleavage of the Gag precursor, which ultimately leads to substantial rearrangements of the capsid (CAp24) molecule involving both inter- and intra-molecular contacts of the CAp24 molecules. In this aspect, Asp51 which is located in the N-terminal domain of HIV-1 CAp24 plays an important role by forming a salt-bridge with the free imino terminus Pro1 following proteolytic cleavage and liberation of the CAp24 protein from the Pr55Gag precursor. Thus, previous substitution mutation of Asp51 to alanine (D51A) has shown to be lethal and that this invariable residue was found essential for tube formation in vitro, virus replication and virus capsid formation.
We extended the above investigation by introducing three different D51 substitution mutations (D51N, D51E, and D51Q) into both prokaryotic and eukaryotic expression systems and studied their effects on in vitro capsid assembly and virus infectivity. Two substitution mutations (D51E and D51N) had no substantial effect on in vitro capsid assembly, yet they impaired viral infectivity and particle production. In contrast, the D51Q mutant was defective both for in vitro capsid assembly and for virus replication in cell culture.
These results show that substitutions of D51 with glutamate, glutamine, or asparagine, three amino acid residues that are structurally related to aspartate, could partially rescue both in vitro capsid assembly and intra-cellular CAp24 production but not replication of the virus in cultured cells.
- CAp24 Protein
- Capsid Assembly
- Turbidity Assay
- Capsid Formation
- CAp24 Antigen
The HIV-1 Pr55Gag precursor, which comprises the inner structural proteins of the virus, is sufficient for assembly of retrovirus-like particles in mammalian cells. During HIV-1 assembly and maturation, the transformation of the virus from a spherical to a conical core structure results as a consequence of substantial inter- and intra-molecular rearrangements of one of the Pr55Gag derived proteins, namely the capsid protein (CAp24). This process is initially driven by the viral protease which sequentially cleaves Pr55Gag and liberates the mature structural proteins that forms the viral core structure [1, 2]. The mature conical HIV-1 core, which is composed of approximately 1500 CAp24 molecules , is comprised of two independently folded subunits, the N- and C-terminal domains (NTD and CTD) . The N-terminal domains of CAp24 are assembled into hexameric rings  and each hexameric ring is joined to the neighbouring ring by the CTDs of CAp24 resulting in a lattice with local p6 symmetry.
Since mutation of Asp51 to alanine has shown to be critical for proper capsid formation and subsequent replication of the virus, we extended the above findings and examined amino acid substitutions of this invariable residue to asparagine, glutamate, and glutamine. All three amino acid residues closely resemble aspartate and were anticipated not to grossly interrupt the CAp24 structure. We designed the mutated Cap24 sequences in both prokaryotic and eukaryotic expression systems and studied their effects in vitro, as well as, in vivo. Two of the three mutants (D51E and D51N) were stable in vitro as was evidenced by forming highly polymerized capsid tubular structures that were closely resembling wild type structure, however, the infectivity and in vivo morphological structures of all three mutants were severely affected.
Viral protein expression of HIV-1 CAp24 mutants
In vitro CAp24 assembly
Morphological analysis of structures formed by recombinant HIV CAp24 in vitro
Analysis of virus release and infectivity
The effect of the three CAp24 mutations on virus infectivity was then assessed with culture supernatants from transfected HeLa-tat III, 293T and COS7 cells. MT4 cells were infected with equal amount of cleared and filtered culture supernatants (normalized for CAp24 antigen) and assayed for CAp24 antigen contents with a CAp24-ELISA three days post-infection (Figure 6B). While none of the three mutant viruses were able to replicate, as expected, the wild type virus replicated in this cell line. Similar results were also seen when the infectivity of mutant viruses was tested in H9 cells (data not shown). We kept the infected H9 cell cultures for more than 25 days without detecting virus replication with the mutants. No revertants to wild type virus were observed.
Single cell cycle infectivity of HIV-1 CAp24 mutant virions
Immunofluorescence analysis of viral protein expression in transfected cells
Effect of HIV-1 CAp24 mutations on virion morphology
Proper structural rearrangement of capsid (CAp24) after Pr55Gag cleavage is a highly conserved feature in most retroviruses . As a result of this process, a β-hairpin structure formed by a salt-bridge between Pro1 and Asp51 (D51) of HIV-1 is important for conformational stability of the N-terminal CAp24 structure . Thus, mutations of D51 in HIV-1 CAp24, and likewise Asp54 in murine leukemia virus (MLV) or human T-cell leukemia virus-1 (HTLV-1), has been shown to disrupt formation of this β-hairpin structure [6, 8, 12].
Structural and mutagenesis studies of D51A mutation in HIV-1 CAp24 has previously shown this invariable residue to be essential for tube formation in vitro, and for the replication and capsid formation in cultured virus . We here demonstrated that substitution of D51 with glutamate (D51E), asparagine (D51N), but not glutamine (D51Q) (three amino acids which in proteins have similar properties as aspartate; Glu > Asn > Gln) could partly restore in vitro CAp24 assembly but not the infectivity of the virus particles.
Whereas generally the total protein contents produced by transfected 293T and COS7 cells were reduced as compared to HeLa-tat or HeLa-tat III cells, similar Pr55Gag-processing patterns was repeatedly observed in all mutant and wild type proviral DNA transfected cells. However, intracellular concentrations of CAp24 protein in any of the cells transfected with D51N and D51Q were generally reduced. This could not be explained by the lack of recognition by the antibody used for immunoblotting, since detection with mouse anti-CAp24, rabbit anti-CAp24 or a pool of sera from HIV-infected patients gave similar results. Additionally, analysis with CAp24-ELISA using a different rabbit anti-CAp24-specific antibody also gave similar results. TEM analysis revealed that all mutants were assembly competent but produced virus particles with aberrant core morphology. The virus particles were also able to incorporate HIV-1 glycoprotein but the infectivity of the virus particles was severely reduced or absent suggesting that there was no defect at binding or internalization of these mutants although this was not specifically tested for. Whereas no infectivity was observed with the D51N and D51Q virions, a subtle amount was seen with the D51E viruses in a single cell cycle infectivity assay.
Further analysis of cytoplasmic versus cell membrane CAp24 distribution was also performed with indirect immunofluorescence staining using mouse anti-CAp24 antibody. This analysis revealed a strong staining pattern near or at the plasma membrane (PM) of cells transfected with the three mutants, indicating that there was no defect in intracellular transport of the Pr55Gag precursor to its steady-state destination  where activation of the viral protease takes place [14, 15]. However, all mutants displayed a decreased cytoplasmic staining as compared to the wild type CAp24 control, which showed a diffuse cytoplasmic staining of non-membrane bound Pr55Gag/CAp24. Perhaps mutated Pr55Gag trafficking and/or assembly is slowed down, or even blocked close to or at the PM in agreement with low levels of mutant particles released. It is also possible that the virus release may have been blocked as a result of inability to form the stabilizing β-hairpin structure in the N-terminal domain of CAp24 upon proteolytic maturation which is necessary for assembly and release of virions .
Self-associative properties of many viral CAp24 proteins have been previously reported [16–19]. However, depending on the protein concentration, salt, and the buffering pH [9, 20, 21], the morphology of the assembled structures or the rate of assembly may be variable. The effects of D51 mutations on in vitro CAp24 assembly was monitored spectrophotometrically, and as expected, the assembly rate of both D51N and D51E mutants were substantially reduced relative to the wild type protein, although the ability of these mutants to form tubular structures was shown by thin-section transmission electron microscopy (TEM). Thus, it seems likely that the D51N and D51E mutations impose less structural changes than the D51A mutation described earlier . Remarkably, although no tubular structure was observed with the D51Q mutant by TEM analysis, an increased optical density measurement that reflects the assembly kinetics was repeatedly observed. We cannot explain this, but, it is possible that the increased OD may result as a consequence of amorphous aggregates that are resistant for stable higher-order CAp24 tube formation.
In a recent study that was published after the present work was performed, Leschonsky et al  described the two single amino acid substitution mutations, a D183E and D183N, in an infectious provirus clone HX10. In contrast to our results, they found no effect on extracellular level of the CAp24 protein produced from H1299 cells transfected with the D183E mutant. Additionally, they found no effect on the intracellular level of the CAp24 protein in H1299 cells transfected with the D51N mutant. This may have been owing to the different cell type used. However, we analyzed the viral protein expression profiles in four different cell lines and found similar results.
Lastly, in order to correlate the lack of infectivity with morphological appearances of the viruses, electron microscopy analysis was performed. Only the D51E mutant particles were partially able to form immature- and mature-like viruses that resembled the wild type morphology. Importantly, despite the ability to form wild type-like viruses, the infectivity of D51E virions was significantly reduced, indicating the importance of optimal HIV-1 core stability . With the two other non-infectious mutants, particles with aberrant core structures, either hollow-shaped spherical structures in endosomal vesicles (D51N) or particles with distorted core morphology (D51Q) were seen.
Taken together, our data and the other previously published observations [6, 22, 24] suggest that the invariable D51 residue of HIV is crucial for formation of the β-hairpin structure in matured CAp24 protein. Additionally, even substitution of D51 with such a similar residue as with glutamate could not restore the integrity of this structure. Furthermore, although our results demonstrated that the D51N and D51E substitutions could restore the in vitro tubular formation, the infectivity of all D51 mutation were rendered non-infectious indicating that this residue is indispensable.
Cells and reagents
HeLa-tat, 293T, COS7, and TZM-bl cell lines were maintained in Dulbecco modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum (FBS), penicillin and streptomycin sulphate (Sigma, St Louis MO). H9, Jurkat-tat and MT4 cells were maintained in RPMI 1640 medium (Gibco, Grand Island, NY) supplemented with 10% fetal bovine serum (FBS; GIBCO), penicillin (100 U/ml), and streptomycin (100 μg/ml). DEAE-dextran was purchased from Sigma, rabbit polyclonal antibodies against calnexin from Santa Cruz Biotechnology (catalogue no. sc-11397). The following reagents were obtained through the AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH: All adherent cell lines, the protease inhibitor indinavir sulphate (catalogue no. 8145) and TZM-bl cells (catalogue no. 8129) contributed by Dr. John C Kappes .
Plasmid DNA construction
The polymerase chain reaction (PCR) was utilized to develop all plasmids in the study and all constructs were derivatives of the HIV-1 molecular clone pNL4-3 . The HIV-1 CA coding sequence was amplified using PCR and cloned into the prokaryotic expression vector pET11a (Novagen Inc.) essentially as described elsewhere [21, 26]. Briefly, the primer pair 5'-ATG GAT CCA TAT GCC TAT AGT GCA GAA CCT CC-3' and 5'-ATG GAT CCT ATC ACA AAA CTC TTG CTT TAT GGC C-3' containing the BamHI/NdeI and BamHI, respectively, were used for amplification of the CA sequence (BamHI/NdeI and BamHI sites are shown in bold). In addition, a translational start codon at the 5' end (ATG) and two stop codons (TGA/TAG) at the 3' end of the sequence were added. The PCR product was subcloned into the TA cloning vector (Invitrogen), transformed in DH5α E. coli (Escherichia coli), purified and confirmed by sequencing (Cybergene, Sweden). The vector was then digested with NdeI and BamHI and the DNA fragment encoding CA gene was isolated, purified and cloned directionally into the pET11a vector, digested with the same restriction enzymes. Standard procedures were used for restriction digestion. The resulting plasmid was designated pET11a-CA and verified by sequencing.
Primers used to create the D51N, D51E and D51Q CAp24 mutants
The same mutations were also introduced into the HIV-1 molecular clone pNL4-3Δenv using the same mutagenic primers described above. QuickChange II XL site-directed mutagenesis kit (Stratagene) was used to create the point mutations in the CA sequence. All plasmid DNAs were then propagated in E. coli XL10-Gold and purified by Maxiprep Purification kit (Qiagen). The identity of each mutation was confirmed by sequencing and the resulting plasmids were digested with BssHII and ApaI. The 1295 bp BssHII/ApaI DNA fragments of the mutated CA sequences were then isolated, purified and cloned directionally into the pNL4-3 vector, digested with the same restriction enzymes. The resulting plasmids were propagated in DH5α competent E. coli, purified using Maxiprep purification kit and verified by sequencing.
Capsid protein expression and purification
Competent E. coli Origami (DE3) cells were transformed with the three mutants or the wild-type pET11a-CA expression plasmid, expressed and purified essentially as described elsewhere . Briefly, a single colony from a freshly streaked plate was initially grown in 50 ml LB-medium containing 100 μl Ampicillin (stock 100 mg/ml) and cultured at 37°C shaken at 220 r.p.m. Upon reaching optical cell densities at 600 nm (OD600) ~0.6–1.0, the cells culture was saved at 4°C overnight. The following day, 10 ml of culture was added to 1 litre of LB-medium containing ampicillin and incubated with shaking at 37°C until the OD600 was ~0.7–1.0. Protein expression was then induced by addition of isopropylthio-β-D-galactoside (IPTG) to a final concentration of 1 mM. After a 4 hrs incubation period at 37°C, the cells were harvested by centrifugation at 4000 r.p.m. for 10 min (Megafuge 2.0 R, rotor #8155, Kendro). The cell pellet was resuspended in 6 M Guanidine-HCl (pH 6.5) and stirred for 3 hrs at room temperature before being centrifuged at 10000 r.p.m. for 10 min at 4°C (Beckman Avanti J30-I, rotor 25.50, Beckman Coulter). Fifty ml of nuclease-free water was slowly added to the supernatant giving a final concentration of 1 M Guanidine-HCl to the protein solution. The protein solutions were put in four 15 cm long dialysis tubings (Spectrpor, MWCO 6–8000, 1.7 ml/cm) and dialyzed against 50 mM Tris pH 8.0 overnight at room temperature. Next, the contents of the dialysis tubings were pooled and centrifuged at 10000 r.p.m. for 10 min at 4°C (Beckman Avanti J30-I, rotor 25.50, Beckman Coulter) to remove precipitated proteins. The CAp24 proteins were then precipitated by addition of saturated (NH4)2SO4 to a final concentration of 30% and incubated on ice for 1 h. The CAp24 proteins were then collected by centrifugation at 20000 r.p.m. for 20 min at 4°C (Beckman Avanti J30-I, rotor 25.50, Beckman Coulter). Finally, the protein precipitate was dissolved in a buffer containing 50 mM Tris-HCl pH 8, 30 mM NaCl and 1 mM EDTA, and purified on ÄKTA FPLC chromatography system (Amersham Biosecience). The protein samples were initially loaded onto an anion-exchange column, HiTrap DEAE 1 ml FF, with a mobile phase of 50 mM Tris pH8.0, 30 mM NaCl, and 1 mM EDTA and flow rate of 1 ml/min. The absorbance was measured at 280 nm. The peak fractions containing the CAp24 proteins were pooled and precipitated with 50% saturated (NH4)2SO4 on ice for 1 h. The solution was then centrifuged at 20000 r.p.m. for 20 min at 4°C (Beckman Avanti J30-I, rotor 25.50, Beckman Coulter) and the precipitate was resupsended in 50 mM Tris pH8.0, 30 mM NaCl, and 1 mM EDTA. The purity and integrity of each CAp24 protein was finally analyzed by SDS-PAGE. In order to increase the purity of the CAp24 protein, the samples were loaded onto a gel filtration column, HiLoad 16/60 Superdex 75 prep grade, and run with the same mobile phase and as above but with a flow rate of 1.5 ml/min. The peak fractions containing the CAp24 proteins were pooled and concentrated by Amicon Ultra Centrifugal filters (Millipore; MWCO 5 k) and saved in aliquots at -80°C. A small aliquot (10 μl) was run on SDS-PAGE gel and the protein concentration was determined with a Bio-Rad DC Protein Assay Kit.
Transfection was performed in a 6-well culture plate using the non-liposomal FuGENE 6 transfection reagent (Roche). Approximately 1 × 105 adherent cells (HeLa-tat, 293T, and COS7) were seeded one day before and transfected with 2 μg of each plasmid DNA mixed with 6 μl FuGENE 6 transfection reagent. Forty-eight to seventy-two hrs post-transfection, cells were washed in cold PBS and harvested in 1× RIPA buffer [50 mM Tris (pH 7.4), 150 mM NaCl, 1% Triton X-100, 1% Na-deoxycholate, and 0.1% SDS] supplemented with a complete protease inhibitor cocktail obtained from Roche.
Virus stock preparation
Wild type and mutant virus stocks were prepared essentially as described before . Briefly, HeLa-tat, COS7, and 293T cells were transfected as described above and three days post-transfection, culture supernatants were clarified from cell debris by centrifugation at 1200 r.p.m. for 7 min, and filtered through 0.45 μm filters. Cleared culture supernatants were then treated or not with DNase I (Roche Applied Science) at 20 μg/ml final concentrations at 37°C for 1 h and saved at -80°C until needed. The CAp24 antigen contents of each culture supernatant was determined by an in-house HIV-1 CAp24 antigen ELISA as previously described [27, 28].
HeLa-tat, COS7, and 293T cells were transfected with the wild type and mutant proviral DNAs as described above. Approximately seventy-two hrs post-transfection, virion-associated viral proteins were prepared from cell culture supernatants by removal of cellular debris by centrifugation at 1 200 r.p.m. for 7 min and filtering through a 0.45-μm-pore-size membrane. The virus particles in the culture supernatants were then concentrated by centrifugation using Viraffinity (CPC Inc.) essentially as described before . Briefly, clarified culture supernatants were mixed with Viraffinity (3:1) and the mixture was incubated at room temperature for 5 min. They were then centrifuged at 1 000 × g for 10 min and viral pellets washed twice in a buffer containing 60 mM HEPES, 150 mM NaCl, pH 6.5. Finally, the viral pellets were dissolved in 1× RIPA buffer, mixed with 2× SDS sample buffer and boiled for 5 min before being subjected to sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).
Denatured whole cell extracts or viral lysates were separated on 10–20% SDS-PAGE gels (Invitrogen), transferred onto a nitrocellulose membrane (Amersham Bioscience) overnight at 4°C and detected either with monoclonal anti-CAp24 antibody (kindly provided by Dr Hinkula J), polyclonal anti-CAp24, anti-cyclophilin A, anti-calnexin (Santa Cruz) antibodies or a cocktail of three different HIV-1 positive human sera. As a secondary antibody, appropriate horseradish peroxidase-conjugated anti-mouse (DAKO; 1:4000), anti-rabbit (Sigma; 1:40000), or anti-human (Pierce; 1:20 000) IgG antibody was used.
Viral infectivity assay
The mutant and wild type HIV-1 virus stocks were prepared as described above and 100 ng CAp24 antigen equivalents were used to infect MT4 cells. Briefly, 1 × 105 cells were infected with normalized amounts of virus for 3 hrs at 37°C. The cells were then pelleted, residual virus was removed, and the cell cultures were incubated in fresh complete medium supplemented with FBS and antibiotics at 37°C in 5% CO2. Three days post-infection, the CAp24 antigen contents in the culture supernatants were then processed for CAp24-ELISA.
Single cell cycle infectivity assay
TZM-bl cells (6 × 104 cells per 12-well plate)  were seeded one day before infection. Following day, medium was removed and cells were infected with mutant and wild type NL4-3 virus. The cells were infected with a virus stock corresponding to 50 ng CAp24 antigen per well with 20 μg/ml DEAE-dextran in a total volume of 300 μl. After adsorption period of 3 hrs, input virus was removed and cells were fed with a complete DMEM containing 10 μM indinavir and cultured for 24 hrs. Finally, culture supernatants were removed and cells were lysed with 200 μl Glo lysis buffer (Promega). One-hundred μl of the cell lysates were then assayed for luciferase activity using the luciferase assay kit obtained from Promega as recommended by the manufacturer. Measurement of the luminescence was done using the Luminoskan Ascent luminometer (ThermoLabsystem).
In vitro HIV-1 CA assembly (Turbidity assay)
Turbidity assay is a valuable technique used to study a salt-induced self-assembly process of CAp24 by monitoring polymerization of CAp24 spectrophotometrically, as the rate of CAp24 tube formation increases sample turbidity [9, 30, 31]. The assay was performed at room temperature using a BioSpec-1601E spectrometer (Shimadzu) and the absorbance was set to 350 nm wavelength. One-hundred μM of highly purified HIV-1 CAp24 protein of each mutant and the wild type control was mixed with 50 mM NaH2PO4 (pH 8.0). Tubular CAp24 assembly was then induced by addition of 2.0 M NaCl solution, and the assembly rates was monitored by a spectrophotometer as the rate of tube formation increases the sample turbidity. Absorbance measurements were made every 10 s for up to 60 min. The assembly rate was then set by plotting the absorbance versus time.
For TEM analysis, 100 μM of each mutant and the wild type CAp24 protein was mixed with 50 mM NaH2PO4 (pH 8.0) and 1.0 M NaCl solution. The mixture was then immediately transferred to a 37°C and incubated for 1 h. Finally, the samples were fixed with freshly made 2.5% formaldehyde and processed for TEM analysis.
HeLa-tat III cells (1.5 × 103 cells per well in 4-well chambered slides from Nunc) were cultured one day before and transfected with 2 μg of mutant and wild type proviral DNA constructs. Forty-eight hrs post-transfection, cells were fixed in aceton/methanol (1:1) for 5 min and washed with PBS. Slides were then incubated with primary anti-CAp24 monoclonal antibody and 4',6-diamidino-2-phenylindole dihydrochloride (DAPI) at 37°C for 1 h. DAPI was used to labell the cellular DNAs. Cells were washed three times in PBS and further incubated with secondary antibody for 1 h. FITC-conjugated rabbit anti-mouse IgG antibody (DAKO) was used as secondary antibody. After the final wash, slides were mounted and flourescent images were aquired by using a Nikon Eclipse E600 phase-contrast fluorescent microsope.
Transmission electron microscopy analysis
Cells were prepared for electron microscopy essentially as described elsewhere . Briefly, transfected HeLa-tat cells and virus infected Jurkat-tat cells (data not shown) were fixed by freshly made 2.5% glutaraldehyde in phosphate buffer and post-fixed in 1% OsO4. The cells were embedded in epon and post-stained with 1% uranyl acetate. Epon sections were cut at approximately 60 nm thick to accommodate the volume of the core structure parallel to the section plane. Duplicate sample preparations were done, which were then analyzed by electron microscope.
Additionally, in vitro assembled CAp24 proteins were negatively stained with 2% ammonium molybdate at pH 8.0 to study the CAp24 tubular formation.
We thank Alireza Padjand for help with the cloning and initial characterization of the prokaryotic expression plasmids. This work was supported by grants from the Swedish Medical Research Council (grant no. K2000-06X-09501-10B), Swedish International development Cooperation Agency, SIDA (grant no. 2006-0011786) and Tripep AB.
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