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Immunotoxins (ITs), which consist of antibodies conjugated to toxins, have been proposed as a treatment for cancer and chronic infections. To develop and improve the ITs, different toxins such as ricin, have been used, aiming for higher efficacy against target cells. The toxin pulchellin, isolated from the Abrus pulchellus plant, has similar structure and function as ricin. Here we have compared two plant toxins, recombinant A chains from ricin (RAC) and pulchellin (PAC) toxins, for their ability to kill HIV Env-expressing cells. In this study, RAC and PAC were produced in E. coli, and chromatographically purified, then chemically conjugated to two different anti-HIV monoclonal antibodies (MAbs), anti-gp120 MAb 924 or anti-gp41 MAb 7B2. These conjugates were characterized biochemically and immunologically. Cell internalization was studied by flow cytometry and confocal microscopy. Results showed that PAC can function within an effective IT. The ITs demonstrated specific binding against native antigens on persistently HIV-infected cells and recombinant antigens on Env-transfected cells. PAC cytotoxicity appears somewhat less than RAC, the standard for comparison. This is the first report that PAC may have utility for the design and construction of therapeutic ITs, highlighting the potential role for specific cell targeting.
Pulchellin is a member of type II ribosome-inactivating protein (RIP) family found in the seeds of Abrus pulchellus tenuiflorus, with four isoforms (termed P I, P II, P III and P IV)1, 2. Other members of this family include abrin, volkesin, ebulin, viscumin and the most extensively studied among all RIPs, ricin3, 4. These type II RIPs, with an approximate molecular weight of 56–65kDa, are composed of an enzymatic A-chain, with the toxic rRNA-specific N-glycosidase activity5, covalently linked by a single disulfide bond to a slightly larger B chain6, 7, a lectin subunit that mediates cell entry8. The A chain of most RIPs, in combination with targeting agents, has anticancer9, antiviral10, 11 and antifungal activities12.
Many studies have been performed with separated toxin A-chain conjugated to carriers capable of delivering them to target cells9, 13. This can be achieved by linking them to monoclonal antibodies (MAbs), to form immunotoxins (IT) or other cell-binding conjugates capable of specifically killing cancer cells14–19 or some infected cells, such as HIV infected cells20, 21.
Ricin (from Ricinus communis seeds) was recognized more than a century ago, while Abrus pulchellus seeds were discovered within the last 30 years1, 22. Our previous studies showed similarities between pulchellin and ricin regarding their structural properties and biological functions1, 2, but there have not been any published reports using pulchellin in targeted therapy. To address this, here we study the use pulchellin A chain (PAC) as an anti-HIV IT. Our previous in vitro studies have shown that anti-HIV ITs based on ricin A chain (RAC) are highly effective antiviral agents, killing HIV infected T cells with great specificity23–25. The envelope glycoprotein (Env) of HIV is the only intact virus protein expressed on the surfaces of virions and infected cells26. Therefore, anti-HIV ITs must be targeted to Env27. Env consists of gp160 (precursor), gp120 (extracellular domain), and gp41 (transmembrane domain) glycoproteins.
We have conjugated recombinant PAC and RAC to two different anti-HIV monoclonal antibodies (MAbs), anti-gp120 MAb 92424 or anti-gp41 MAb 7B228. We performed a side-by-side comparison of their ability to bind, enter and kill HIV infected cells (H9/NL4–3)27, 29 or Env-transfected 293T cells30, as well as their non-specific toxicity on uninfected or non-transfected parental cells. The efficacy of anti-gp41 ITs was studied in the presence and absence of soluble CD4 (sCD4)31. In this paper we demonstrate that PAC can function within an effective and specific IT, with slightly less efficacy than RAC. An irrelevant antibody conjugated to either RAC or PAC had no effect.
PAC and RAC were produced as recombinant proteins in E. coli. After purification of 6xHis tag-removed product by Sephacryl S-200 column, fractions containing purified PAC or RAC were concentrated to 2mg/ml. Full details are described in Supplementary Information. MAbs were produced in tissue culture supernatants and purified on Protein A agarose beads. MAbs and toxin A chains were tested for purity and size by microcapillary electrophoresis (Fig. 1). Results demonstrate the appropriate size for full length MAbs (H and L chain) with approximately 150 and 157kDa for 924 and 7B2 MAbs, respectively. Both RAC and PAC are 27kDa.
We optimized the conjugations of RAC and PAC to MAbs 924 and 7B2, in parallel, by applying different concentrations of LC-SPDP bifunctional cross linker (10, 20 and 40-fold molar excess of LC-SPDP). The results of microcapillary electrophoresis analysis under reducing and non-reducing conditions of the 924-ITs and 7B2-ITs are shown in Fig. 1B. The conjugates with 40-fold molar excess of LC-SPDP biolinker gave major bands of the predicted molecular weights for one and two toxin A chains per antibody molecule (approximate MW, 180,000 and 210,000, respectively) and a minor band of MW 240,000 representing three toxin A chains per antibody molecule (see Supplementary Fig. S1). Under reducing conditions, the conjugates showed three characteristic bands corresponding to light and heavy chains, and the toxin A chains (see Supplementary Fig. S1). By comparing toxin A chains, both RAC and PAC were conjugated equally to 924, however with 7B2 we obtained a superior conjugation with PAC. Then, the conjugates with 40-fold molar excess of biolinker passed from Ultra-100K centrifugal filter. As Fig. 1C shows, by 40-fold molar excess of crosslinker, we could reach to optimum IT with almost eliminated free MAb. In Fig. 1D, the Electropherogram of ITs (40 x ones) shows the total protein mass of RAC and PAC ICs were containing only 3.9% and 2.7% free 924 MAb, respectively.
By using an indirect ELISA, we tested the ability of purified MAb 924 and 924-based ITs to bind recombinant gp120(IIIB) antigen and V3 loop peptide. In parallel, the binding ability of MAb 7B2 and 7B2-based ITs were examined by using the gp41 loop peptide antigen. In Figs Figs2A2A and and3A,3A, all the purified MAbs and conjugates bound to the appropriate antigens, while the isotype controls (MAbs and MAb-RAC) and negative control (plate coated with unrelated control ligand) did not, demonstrating that immunologic specificity of the antibodies in the ITs was unaffected by the conjugation process. Moreover, the results demonstrate that the different concentrations of biolinker did not significantly affect the function of the conjugated MAb (see Supplementary Fig. S1). Besides, we examined the ability of anti-ricin A chain MAb RAC18 to bind recombinant RAC (rRAC) and recombinant PAC (rPAC). As has previously been reported32, RAC MAb18 bound to rRAC, with no binding to the isotype control MAb 924. Interestingly, RAC MAb18 showed a binding ability to rPAC as much as rRAC (Fig. 2B).
We examined binding to native Env by flow cytometry, using FITC conjugated goat anti-human or Alexa488 conjugated goat anti-mouse IgG secondary antibody to detect IT binding. 924-based ITs bound to persistently infected H9/NL4–3 cells (Fig. 2C). 7B2-based ITs bound to H9/NL4-3 cells28 as well as to 293T cells transfected with 92UG037.8 gp160 (Fig. 3B–D). ITs did not bind uninfected H9 or 293T cells, confirming the specific cell binding of ITs. Addition of sCD4-183 enhanced binding of 7B2-based ITs to Env-transfected 293T cells (Fig. 3B), as has previously been reported for RAC-7B225, 31. We directly labeled ITs to Alexa488 for later experiments. Figure 3D shows direct fluorescence with the ITs and naked 7B2 after Alexa488 labeling.
To quantify the internalization of ITs by flow cytometry, the Env-transfected 293T cells were incubated with Alexa-labeled ITs in the presence or absence of 0.05% sodium azide (Na Az). Prior to cytometry external fluorescence was quenched with trypan blue (TB). Given that TB enters dead cells and may interfere with the fluorescent analysis, we confirmed high cell viability (96%). In the presence of NaAz, ITs cannot be internalized, they only bind to antigens on the cell surface. The addition of an increasing concentration of TB showed that 3mg/ml of TB was sufficient to quench extracellular fluorescence (Fig. 4A). However in the absence of NaAz this concentration of TB caused no quenching (Fig. 4A), indicating the Alexa-labeled ITs were internalized, although we cannot rule out a small amount was bound to the cell surface. Figure 4B demonstrates the population of cells in the absence of TB, with 7B2-PAC-Alexa488, either bound to the cell membrane or internalized. We also observed a negligible population of cells without Alexa-labeled ITs. After addition of TB, the green fluorescence emission was not quenched, signifying the 7B2-PAC-Alexa was internalized. Moreover, the upshift of cell population corresponded to the cells with damaged membrane (dead cells) and Alexa-labeled ITs adherent to the membrane which emitted red fluorescence after quenching. Figure 4C shows the same results for 7B2-RAC-Alexa488.
Internalization of ITs was confirmed by live confocal microscopy of Env-transfected cells with 7B2-PAC-Alexa488. After the addition of IT, live imaging included approximately 50 observations during the 90min period. In Fig. 4D, after 15min of incubation, the IT was observable on the cell surface, and after 30min, was identified intracellularly as small vesicles. Following 90min, the imaging of one specific region before and after TB addition demonstrated quenching of the green fluorescence on the cell surface and emitting red fluorescence (shown by white arrow in Fig. 4D).
The localizations of 7B2-PAC and 7B2-RAC were studied by non-quantitative confocal microscopy. Env-transfected 293T cells were incubated with Alexa488-ITs and BFA-bodipy under physiologic conditions, or in the cold with sodium azide to block the entry of IT into the cell. Serial vertical sections are shown in Fig. 5. In the presence of azide (Fig. 5A), ITs only bound to the cell surface, whereas under physiologic conditions 7B2-PAC or 7B2-RAC were observed on the cell surface and internalized. The areas of yellow signal demonstrate the colocalization of internalized IT (green signal) on the ER and Golgi colored by BFA-bodipy (red signal).
To test biological activity of ITs, we used a direct cytotoxicity assay in two experiments: In the first experiment, we used H9/NL4-3 infected T cells to test the cytotoxicity of 924-based ITs. In the second, we assayed the cytotoxicity of 7B2-based ITs, including Alexa-labeled and unlabeled versions, to Env-transfected 293T cells in the presence or absence of sCD4. In each experiment, the cells were incubated with differing concentrations of ITs or MAbs as control. The other controls included; no cells (background) and cells in the absence of IT. Cell viability was measured after 3 days by MTS dye reduction, with a decrease in A490 indicating cell death (Fig. 6 and S2). The results demonstrate the efficacy and specificity of each IT for the infected cells, but not uninfected cells. Although 924-PAC appeared less efficacious than 924-RAC, these results were not observed with 7B2-PAC and 7B2-RAC. The amount of LC-SPDP used for the conjugation had little effect on IT efficacy (Fig. S2). The cytotoxicity of ITs used in imaging analyses was unaffected by Alexa conjugation (Fig. 6C).
To develop improved ITs, different toxic domains have been used, aiming for higher toxic efficacy or fewer undesired effects14. Pulchellin toxin is a type II RIP, structurally similar to ricin22, 33. Moreover, the A chains of both ricin and pulchellin contain only one cysteine residue for forming an interchain disulfide bridge2, 34. In spite of the similarities in the structure of ricin and pulchellin, the anti-viral and anti-tumor activities of RAC have been studied well3, 35, 36, while there are no published data to exploit the feasibility of using PAC in targeted therapy. Here we have explored the function of PAC as an IT candidate, when coupled to MAbs to the HIV envelope, the only intact virus protein expressed on the surfaces of virions and infected cells.
We have conjugated two different anti-Env Abs to RAC and PAC, then tested their cytotoxic activity on either persistently infected or transfected cell lines. The results clearly indicate the efficacy of PAC-containing ICs. The comparative efficacy of PAC vs the well-studied toxic moiety RAC is not fully resolved, with one set of experiments using 924 MAb showing PAC to be slightly less efficacious than RAC, but the set of experiments with 7B2 ITs showing no difference. Within the range we tested, the concentration of bifunctional crosslinker did not appear to have a significant effect on the binding ability of the conjugates (see Supplementary figures S1 and S2). There is only one free cysteine on PAC (Cys247) which reacts with MAb-linker rapidly in high yield without diminishing biological activity of toxin. SPDP can crosslink with multiple alternative amino groups on the MAb37, 38. This may affect on the MAb binding ability (not the A-chain toxicity), while we have shown by ELISA and FACS which is not affected.
In this study we tested the 924 ITs on persistently infected H9/NL4-3 cells. The Env expressed by this virus is the prototypical laboratory strain IIIB, and MAb 924 binds uniquely to the tip of the V3-loop of this isolate. MAb 7B2 binds a well conserved epitope in the helix-loop-helix region of gp41. The peak table in Fig. 1D, demonstrates a stoichiometric similarity between PAC and RAC ICs, regarding in the number and percentage of the linked A-chains. This similarity of stoichiometric heterogeneity may not affect the interpretation of the cytotoxicity assay during comparison between RAC and PAC ICs. The efficacy of 7B2-RAC ITs has been studied extensively in a variety of HIV infected cells, and more recently in Env-transfected 293T cells. The efficacy of 7B2 ITs has been demonstrated in vivo 28, 39. Here we have used cells stably transfected to express fully functional envelope (gp160, gp120 and gp41) from HIV clade A clinical isolate gp160 (293T/92UG)30 and shown that 7B2-RAC and 7B2-PAC are equivalently cytotoxic. As we have observed previously31, soluble CD4 enhances epitope exposure and IT efficacy. By comparing the susceptibility of these two cell lines, as we have shown before27, 293T/92UG cells are significantly more sensitive to the IT than H9/NL4-3 cells. These differences in IT-mediated killing, between transfected 293T/92UG cells and infected H9/NL4-3 cell lines, are unrelated to the binding of the MAb to the target cells. As we have explained previously27, discrepancies among these two cell lines may reflect differences resulting from transfection versus infection and/or laboratory-adapted versus clinical isolates.
In this study, we demonstrate that PAC stands outs as feasible candidate for the design and construction of effectively specific ITs. In this case, the immunogenicity of PAC will be a matter of great interest; whereas the development of anti-pulchellin Abs will be a major limitation for pulchellin-based immunotoxins. RAC MAb 18 has a common motif of QXXWXXA on the structure of RAC40 and PAC which fold into part of the enzyme active site2. We have demonstrated that RAC MAb 18 binds to not only rRAC also rPAC (Fig. 2B). This finding helps us for our future study on the immunogenicity of PAC.
Our previous microscopy studies have revealed the intracellular localization and trafficking of whole pulchellin and ricin toxins32, 41. Herein, we have used flow cytometry and confocal microscopy to study cell binding, uptake, and intracellular localization of 7B2-PAC. We have used Env-transfected 293T cells for microscopic study, because these cells are adherent in compare to suspension H9 lymphoma cells42. We have shown that 7B2-PAC binds to the cell surface and is internalized, possibly localizing to ER and Golgi, within one hour. We are now studying the intracellular trafficking of PAC immunotoxins.
This is the first demonstration that PAC may have utility for the design and construction of therapeutic ITs, highlighting the potential role for specific cell targeting not only for AIDS also cancer treatment.
H9/NL4-3 cells are laboratory-adapted and persistently infected with the NL4-3 molecular clone of HIV27, 29 and maintain a productive infection in all cells during passage in tissue culture. Uninfected H9 cells, a human CD4+lymphoma cell line, were obtained from Dr. M. Reitz (Institute of Human Virology, Baltimore, MD). H9 and H9/NL4-3 cells were maintained at 37° in 5% CO2 in RPMI 1640 medium with 10% fetal bovine serum (Gibco Invitrogen, Grand Island NY) as described elsewhere23.
293T cell lines stably express clade A clinical isolate 92UG037.8 gp160 as native gp120/gp41trimers (293T/92UG)30. 293T cells were used as uninfected control cells. The transfected and non-transfected 293T cells were maintained at 37° in 5% CO2 in DMEM medium with 10% fetal bovine serum (Gibco Invitrogen, Grand Island NY). In this paper, Env-transfected cells refer to the 293T cells stably transfected with 92UG037.8 gp160.
MAb 924 was produced from a mouse immunized with a vaccinia virus recombinant containing a gene encoding the HIV gp160, as described elsewhere24. This IgG1 antibody reacts with the V3 loop of HIV gp120 of LAV/HTLV-IIIB isolate. MAb 7B2 (Genbank accession numbers JX188438 and JX188439) is a human IgG1 which binds HIV gp41 at AA 598–604 (CSGKLIC) in the helix-loop-helix region28, 31. HY (Genbank accession numbers JX188440 and JX188441), an affinity matured version of the anti-CD4 binding site Ab b1243. Murine and chimeric version of anti-ricin A chain MAb RAC18 and Alexa 488-conjugated RAC18 have been described elsewhere40, as has the isotype control 924 MAb32. MAbs were purified from hybridoma supernatant on Protein A agarose beads (Invitrogen) and eluted with 0.1M glycine, pH 2.5, immediately neutralized, and dialyzed vs PBS. Two types of soluble CD4 were used to observe CD4-mediated effects31; CD4-183 contains the first two domains of CD4 including the region in domain 1 that binds the HIV coat protein gp120. CD4-IgG2 is a tetrameric fusion protein comprising human IgG2 in which the Fv portions of both heavy and light chains have been replaced by the V1 and V2 domains of human CD4. Goat anti-human IgG (Invitrogen) was conjugated to either alkaline phosphatase (AP) or fluorescein isothiocyanate (FITC). Goat anti-mouse IgG (Biacore) (heavy+light chains) secondary antibody was conjugated to Alexa-488.
Recombinant pulchellin A-chain (rPAC) was generated by PCR using the pulchellin cDNA isoform PII2, accession number EU008736.1, as template. In our previous study, the rPAC had a 6xHis-tag at its N-terminal end2, 34. In this experiment, we designed a new construct containing a tobacco etch virus protease (TEV) cleavage site for proteolytic removal of the 6xHis-tag after purification. Specific primer sequences were the following: rPAC-forward (5′ CCCCATGGCTAGCGAGGACCGGCC) and rPAC-reverse (5′GTGCTCGAGTTAATTTGGCGGATTGC), including the restriction sites for NcoI and XhoI, respectively. PCR products were cloned into the pGEM-T (Promega) vector and its sequence was confirmed using an ABI Prism 377 automated DNA sequencer (Genescript). Recombinant RAC was produced in BL21(DE3)RIL cells (Novagen) from plasmid pETtrx, which encodes E. coli thioredoxin and a TEV protease-cleavable 6xHis affinity tag in frame with and N-terminal to the RAC coding sequence. The target sequences of RAC and PAC were subcloned into pET28a(+) vector (Novagen).
Expression and purification of PAC and RAC is described in supplementary data. Briefly, the recombinant PAC and RAC were produced in E. coli Rosetta (DE3), and purified by HisTrap Nickel column. The His-tag was cleaved with TEV protease, and the tag-less toxin A chain was purified on a HiPrep 26/60 Sephacryl S-200 column.
HIV MAbs 924 and 7B2 were conjugated separately to PAC and RAC by using a modification of the protocol described elsewhere23, 24. Optimization of the concentration of heterobifunctional cross-linking reagent succinimidyl 6-[3(2-pyridyldithio) propionamido] hexanoate (SPDP, Pierce) was carried out for conjugation between amino groups (on lysine and at the N-terminus) on antibody and the single free cysteine on A-chain toxin37, 38 by applying three different concentrations of LC-SPDP biolinker (10, 20, and 40X molar excess relative to MAb), as described in supplementary data, figure S1. After 2 hr of incubation at room temperature, the MAbs and SPDP were separated on a Zeba desalting column (Pierce) equilibrated with PBS.
PAC and RAC (1mg in 0.5ml), which were stored at –80°C in reduced form, were desalted on Zeba column. The RAC/PAC and MAb-SPDP were mixed separately, concentrated to 0.5ml and incubated overnight at 4°C. Individual fractions were analyzed by microcapillary electrophoresis (Agilent Bioanalyzer, GE Healthcare). After the conjugation reaction, the removal of unreacted A-chain toxin and holotoxins were achieved by using an Amicon Ultra-100K centrifugal filter (Millipore). The concentrations were measured by bicinchoninic acid protein assay (Pierce, Rockford, IL) and confirmed using OD280 reading by Nanovue UV Spectrophotometer (GE Healthcare, Piscataway, NJ), before and after passing from filter.
ELISAs were performed for Ag-binding specificity analysis and titration of purified MAbs and ITs in wells coated with antigen (1μg/ml), as described elsewhere25. The gp41 antigen was a linear peptide HIV-1 consensus clade B sequence [LGIWGCSGKLICTT] representing the epitope of 7B2. Gp120 antigen was a recombinant protein expressed in mammalian cells. Recombinant gp120 antigen represented HIV isolate IIIB (gift from Genentech, S. San Francisco, CA). The synthetic V3 loop peptide represented the V3 sequence of strain IIIB (amino acids AA 297–330; numbering according to reference 44, TRPNNNTRKSIRIQRGPGRAFVTIGKIGNMRQAH. Binding of antibody to the antigen was detected with AP-conjugated secondary antibodies: goat anti-mouse IgG (H+L chain specific) for HIV MAb 924 as well as 924 based-ITs; or goat anti-human IgG (H+L chain specific) for HIV MAb 7B2 as well as 7B2 based-ITs (all from Zymed Laboratories, South San Francisco, CA). Data are reported as optical density at 405nm and represent means of triplicate values with three independent experiments.
We used indirect immunofluorescence and flow cytometry to analyze binding of immunotoxins to either persistently infected H9/NL4-3 cells, or Env-transfected 293T cells. 8×104 cells were added to IT to reach the final concentrations of 5ng/ml to 5µg/ml. Cells were incubated 1 hr at room temperature. Cells were washed, and then stained with Alexa488-conjugated goat anti-mouse IgG secondary antibody (2μg/ml) for 924 based-ITs; or FITC conjugated goat anti-human IgG secondary antibody (2μg/ml) for 7B2 based-ITs for 1–4hr, washed twice and fixed in 100μl of 2% paraformaldehyde. After a minimum of 4hr, 150μl of PBS was added. Cells (10,000) were studied on a Becton-Dickson LSR II with HTS plate reader, analyzed by Flow-Jo software (Treestar Inc). Forward scatter (FSC) and side scatter (SSC) gated data are represented as either overlayed histograms or as graphs of mean fluorescence. The conjugates or MAbs did not bind to uninfected H9 cells nor untransfected 293T cells.
Labeling was carried out by mixing 1ml of each IT at ~1mg/ml, in sodium phosphate buffer 50mM, pH 7.5, NaCl 0.1M, with 100µg Alexa Fluor 488 as N-hydroxysuccinimide (NHS) salts (Invitrogen Molecular Probes, Eugene, OR). The reaction was maintained for one hour in the dark at room temperature with continuous stirring. Labeled protein was separated from unconjugated dye on Zeba 7KD cutoff desalting columns (Pierce, Rockford, IL). The degree of labeling was determined by measuring the A280 and A495 of the conjugates. ITs were characterized before and after labeling, with aforesaid protocols.
Env-transfected 293T cells (1.5×105) were placed in 100ml in round-bottom 96 well plates (Costar, Lowell, MA) in the presence or absence of 0.05% NaAz for studying, respectively, the binding or internalization of ITs by flow cytometry. Cells were stained with 1.0μg/ml Alexa488-labeled ITs in the presence of 1.0μg/ml sCD4-183 in serum-free medium for 4hr at 4°C. As negative controls, two wells either were stained by ChRAC18 or were left unstained. Cells were washed twice then 250µl of PBS was added, in the presence or absence of 0.05% NaAz. The percentage of cell viability was analyzed by optical microscopy by incubating with 0.4% Trypan Blue (TB, Sigma) solution diluted in PBS to perform the TB exclusion test with counting in a Neubauer chamber. In order to confirm internalization of ITs to the cells, we used a modification of the protocol described elsewhere45–47. An increasing concentration of Trypan Blue from 1 to 3mg/ml was used to quench the extracellular fluorescence. Cells were analyzed under a Becton-Dickson LSR II (BD, Franklin Lakes, NJ) both prior and 2min after TB addition. 10000 events were collected and data analyzed by Flow-Jo software (Treestar, Ashland, OR). Green fluorescence (FL1) of internalized Alexa488-labeled ITs was collected using a 530±30 band-pass filter; red fluorescence emitted from TB bound to Alexa488-labeled ITs on the cell surface (FL3) was collected by using a 650±13 band-pass filter. The data were collected using linear amplification for FSC and SSC, and logarithmic amplification for FL1 and FL3.
Live cell imaging was performed as described elsewhere32. All the images, including those used for quantitative analyses, were obtained with an inverted Zeiss LSM 510 microscope, a 63×1.4 NA oil-immersion objective, and Zeiss LSM software. Heated (37°C) stages and objectives were used on microscope. One day prior to imaging, 104 Env-transfected 293T cells were seeded into 35mm culture dishes with 0.17mm thickness glass bottom (MatTek, Ashland, MA). In parallel, 293T cells were seeded as a control. Cells were cultured at 37°C in DMEM, 10% FCS, puromycin 1µg/ml. The following day, cells were placed into 1ml incomplete RPMI w/o Phenol red at pH 7.4 with 25mM HEPES/1% BSA and transferred to the heated (37°C) stages for confocal microscopy imaging. 7B2-PAC-Alexa488 and sCD4-183 were added to final concentrations of 1µg/ml each. Taking images of different cells started after the addition of Abs, generally 50 observations during the 90min period. Pinhole settings were such that an optical slice was less than 1µm. The intracellular location of Alexa-labeled IT was confirmed by quenching the Alexa488 bound on the surface45. After 90min of imaging, one specific region was analyzed before and after adding 3mg/ml TB. The excitation was at 488nm and Alexa488 fluorescence emission was detected by 530±30 band-pass filter. TB emission was detected by 650±13 band-pass filter.
In one day before confocal experiment, 4×104 cell per well of two cell lines, 293T and Env-transfected-293T cells, were seeded on a multiple-chamber slide (Nalge Nunc International). The next day, in order to block the IT internalization, the media of two control wells were replaced with PBS/BSA/0.01% sodium azide (PBA) 400µl per well for 45min in RT. Then, cells were treated by 1µg Ab/IT in 500µl PBS or PBA, incubated 60min in RT. The antibodies were 7B2-Alexa488, 7B2-PAC-Alexa488 and 7B2-RAC-Alexa488 in the presence of 1µg sCD4-IgG2). The controls were chRAC18 and sCD4-IgG2-Alexa488. One well was left without adding antibody. BFA-bodipy (250ng/ml) was added to cells to demonstrate rapid accumulation of toxins in Golgi and ER. BFA-bodipy was tested to determine that at the concentration used there was minimal effect of the BFA on the cytotoxicity of ITs32. After 2X washing with PBA, the cells were fixed in 2% paraformaldehyde/PBS in 45min. We took out the solution, and removed the slide box, added one drop SlowFade Gold Mountant DAPI (Life Technologies) and covered it by slide glass. Images were obtained with an inverted Zeiss LSM 510 microscope, a 63×1.4 NA oil-immersion objective, and Zeiss LSM software. For each cell, a Z-stack with 1µm steps was imaged.
A cytotoxicity assay was performed to analyze the cell killing ability of ITs The target H9/NL4-3 cells or Env-transfected 293T cells (or their uninfected/untransfected parents as controls) were plated in triplicate in Complete RPMI (Supplement RPMI-1640 medium with 10% FCS and 1% sterile antibiotic) or DMEM plus 10% FCS, respectively, in 96 well flat-bottom tissue culture plates (Costar). Controls included: no cells (background) and cells in the absence of IT or in the presence of naked antibody. Serial dilutions of ITs, including the Alexa-labeled and unlabeled versions, were incubated with cells for 3 days. The incubation of 7B2-based ITs (not 924-based ITs) were in the presence or absence of 300ng/ml of sCD4. For the final 6hr of incubation, MTS/PMS substrate (Promega, Madison, WI) was added to each well and plates read hourly at 490nm. Results represent the mean and SEM of triplicate samples (representative of three independent experiments), and are plotted as A490 with the no cell background subtracted. The percentage of cell viability was quantified by calculating the ratio below:
Statistical analyses were performed using GraphPad Prism, v5.0. Data are shown as mean and SEM of the indicated number of replicate values. If no error bar appears present, the error bars are smaller than, and obscured by, the symbol. The method for statistical comparison is by unpaired two-tailed Student’s t-test, unless specifically indicated otherwise.
All data generated or analysed during this study are included in this published article and its Supplementary Information file.
Special thanks to Prof. Bing Chen from the Department of Pediatrics, Harvard Medical School for the generous gift of 293T cell lines stably transfected with 92UG037.8 gp160s. We acknowledge Children’s Hospital of New Orleans, CAPES and CNPq for the financial support to carry out this research. The authors acknowledge the support provided by: FAPESP (Sao Paulo Research Foundation) –grant numbers: 2013/07276-1(CEPOF – CEPID Program), 2009/54035-4 (EMU). S.H. Pincus was supported by NIH grant U54 GM104940 (Louisiana Clinical and Translational Science Center). We also thank NIH AIDS Research and Reference Reagent Program for supporting the reagent related to HIV.
S.H.P. and M.S. wrote the main manuscript text and prepared figures. F.E.G.G., S.H.P. and M.S. designed and performed the immunological and microscopy experiments. M.S., A.P.U.A., D.K.W. and L.L.J. performed biochemical experiments. S.H.P. and F.E.G.G. supervised the study. All authors reviewed the manuscript.
The authors declare that they have no competing interests.
Electronic supplementary material
Supplementary information accompanies this paper at doi:10.1038/s41598-017-08037-3
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Francisco E. G. Guimarães, Email: rb.psu.csfi@searamiug.
Seth H. Pincus, Email: email@example.com.