- Open Access
Homonuclear 1H NMR and circular dichroism study of the HIV-1 Tat Eli variant
© Watkins et al; licensee BioMed Central Ltd. 2008
- Received: 30 April 2008
- Accepted: 22 September 2008
- Published: 22 September 2008
The HIV-1 Tat protein is a promising target to develop AIDS therapies, particularly vaccines, due to its extracellular role that protects HIV-1-infected cells from the immune system. Tat exists in two different lengths, 86 or 87 residues and 99 or 101 residues, with the long form being predominant in clinical isolates. We report here a structural study of the 99 residue Tat Eli variant using 2D liquid-state NMR, molecular modeling and circular dichroism.
Tat Eli was obtained from solid-phase peptide synthesis and the purified protein was proven biologically active in a trans-activation assay. Circular dichroism spectra at different temperatures up to 70°C showed that Tat Eli is not a random coil at 20°C. Homonuclear 1H NMR spectra allowed us to identify 1639 NMR distance constraints out of which 264 were interresidual. Molecular modeling satisfying at least 1474 NMR constraints revealed the same folding for different model structures. The Tat Eli model has a core region composed of a part of the N-terminus including the highly conserved Trp 11. The extra residues in the Tat Eli C-terminus protrude from a groove between the basic region and the cysteine-rich region and are well exposed to the solvent.
We show that active Tat variants share a similar folding pattern whatever their size, but mutations induce local structural changes.
- Nuclear Magnetic Resonance
- Circular Dichroism
- Circular Dichroism Spectrum
- Nuclear Magnetic Resonance Study
- Circular Dichroism Signal
The human immunodeficiency virus type 1 (HIV-1) trans-activator protein Tat is essential for the activation and expression of HIV genes . Tat interacts with a RNA hairpin-loop structure called the trans-activation-responsive region (TAR) located at the 5' end of all nascent viral transcripts and interacts with an RNase suppressing the processing of small RNAs [2, 3]. However, Tat differs from other HIV-1 regulatory proteins due to its early secretion from HIV-1-infected CD4+ T cells . Extracellular Tat can traverse cellular membranes and induce apoptosis preventing the immune system from eliminating HIV-1-infected cells . Tat is encoded by two exons. The first exon encodes amino acids 1–72 and the second exon encodes amino acids 73–86/101 that contribute to viral infectivity and other functions such as the induction of CD4+ T cell apoptosis .
A vaccine targeting Tat could help restore cellular immunity in HIV-1-infected patients . A recent study using autologous dendritic cells, loaded with exogenous simian immunodeficiency virus peptides that spanned the overlapping reading frames within Tat successfully induced cellular immune responses in rhesus macaques . However, no successful phase II clinical trial targeting Tat has so far been reported . This might be due to the variability of Tat variants, as Tat can tolerate up to 38% sequence variation that modifies its immunological epitopes without a loss in trans-activational activity . Moreover, until now, most Tat vaccine approaches have used the European Tat Bru or HXB2 variant that have 86 residues , while Tat variants found in clinical isolates are predominantly 99 to 101 residues in length and have greater trans-activational activity [2, 6, 12].
All Tat variants with proven biological activity display similar circular dichroism (CD) spectra, while inactivation due to chemical cysteine modification dramatically changes the CD spectrum of Tat . Tat is usually divided into six different regions : region I (residues 1–21) is a proline-rich region and has a conserved Trp 11, region II (residues 22–37) has seven conserved cysteines at positions 22, 25, 27, 30, 31, 34 and 37 (no other cysteines are found in the sequence), region III (residues 38–48) has a conserved Phe 38 and the conserved sequence LGISYG from residues 43 to 48, region IV (residues 49–59) is rich in basic residues and has the conserved sequence RKKRRQRRRPP, region V (residues 60–72) is a glutamine-rich region, and region VI constitutes the C-terminus of Tat encoded by the second exon, but its size depends on the HIV-1 isolates. The nuclear magnetic resonance (NMR) structure of two active Tat variants of 86 and 87 residues (Tat Bru and Tat Mal respectively) showed a similar folding, while amino acid sequence variation led to local structural dissimilarities notably in region V [14, 15]. A part of region I involving the strictly conserved Trp 11 constituted the core region, with the other regions packing around it while being well exposed to solvent. Recently, an NMR study of a peptide corresponding to the first exon of Tat (residues 1–72) showed that no structure could be identified in this peptide .
In this study, we report a complete NMR assignment and structural characterization of a long Tat variant (99 residues) called Tat Eli. HIV-1 Eli is a subtype D primary isolate identified during the 1980's in what was then Zaire . Tat Eli was obtained from solid-phase peptide synthesis and has biological activity as demonstrated in a trans-activation assay. Circular dichroism (CD) experiments indicate that Tat Eli is not a random coil at 20°C. 2D NMR spectra of Tat Eli and molecular modeling revealed a folding similar to Tat Bru and Tat Mal for the first 86 residues. The C-terminal extension is exposed to solvent and is packed between the basic region and the cysteine-rich region.
Synthesis and biological activity of Tat Eli
CD Spectra of Tat Eli
NMR Resonance Assignments
Conserved folding among Tat variants
Tat Eli structure
This is the first NMR study of a long Tat variant (99 residues) with biological activity. CD data show that the synthetic Tat Eli used in our 2D NMR study is not a random coil. We observed similar chemical shifts with the two previous NMR studies of biologically active Tat variants [14, 15] suggesting a common folding for Tat. This is characterized by a central location of the N-terminal region around the highly conserved Trp 11 that is part of a hydrophobic pocket that contains well-conserved aliphatic and aromatic residues.
Our results are different from the NMR study of a peptide corresponding to the first exon of Tat suggesting that Tat is a natively unfolded protein . This study was remarkably well done from the point of view of NMR; however, it was carried out on a peptide that does not correspond to a real Tat protein. Moreover, the sequence used does not correspond to a primary isolate, as a viable HIV-1 strain that expresses only the first exon of Tat has never been observed, and it has been shown that both exons of Tat are necessary for integrated proviruses . Furthermore, the second exon of Tat has important functions for replication in vivo  and is involved in CD4+ T cell apoptosis . We were able to identify long-range NMR constraints with our Tat variants involving the second exon. This could indicate that both exons of Tat are necessary to have stable folding. The first NMR study on Tat was also carried out with an inactive form of Tat due to the reducing conditions used, but long-range NMR constraints were identified with this protein that had both exons .
Previous studies have examined the effect of Zn2+ binding on the structure of Tat with different results [20–22]. We observed no change in the CD spectra in the presence of Zn2+ confirming the results by Frankel et al.  that Zn2+ does not affect Tat folding. However, we proffer no evidence that supports the metal-linked dimer form of Tat. Furthermore, monomeric forms of Tat variants are recognized by antibodies from HIV-1-infected patients [27, 28].
The C terminus of Tat Eli is packed between the basic region and the cysteine-rich region (Figure 6). The second exon of Tat is composed of three β-turns and is well exposed to solvent. Conformational epitopes exist in Tat variants that influence the magnitude and breadth of antibody response against Tat . These mutations do not prevent the biological activity but dramatically change its immunogenic properties . For instance, antibodies raised against Tat Eli have weak avidity against other Tat variants . Interestingly, a Tat variant called Oyi identified in patients who did not progress to AIDS has a 3D epitope that raised antibodies capable of recognizing all Tat variants. Therefore, the humoral immune response against different Tat variants suggests, as our NMR studies suggest, that a conserved folding exists among Tat variants .
Tat Eli has fewer long-range NMR constraints compared to Tat Bru (Figure 5A) and Tat Mal [14, 15]. It is possible that some long-range NMR constraints were not detected due to chemical shift overlaps such as for the rings of Trp 11 and Phe 38 (additional file 1). However, Tat Eli has greater trans-activational activity than both Tat Bru and Tat Mal , which could be due to greater flexibility compared with these two Tat proteins. This may explain the lower number of long-range NMR constraints.
The exact mechanism by which Tat enters cells remains unknown. The high flexibility and high activity of Tat Eli make it a good candidate to study this mechanism. The core of Tat Eli is mainly composed of 10 aromatic residues organized in a hydrophobic cluster. This core region might be involved during Tat internalization, as the mechanism certainly requires a structural change for this hydrophobic environment. Therefore, it might be interesting to study the structure of Tat Eli or fragments of this protein using solid-state NMR  in a hydrophobic environment similar to biological membranes. This, however, is still an ambitious task as it will require uniform (or extensive) 13C, 15N-labelling and thereby the establishment of appropriate systems for large-scale recombinant expression.
In conclusion, this study suggests that biologically active Tat variants share a common folding. This study should help to understand how some antibodies neutralize Tat activity and aid the development of an AIDS vaccine targeting Tat. Tat Eli is one of the most active Tat variants that we have synthesized but this variant does not have the capacity to induce a broad immune response against other Tat variants as Tat Oyi does. Therefore, it would be interesting to determine the NMR structure of Tat Oyi (101 residues) and compare it with Tat Eli. Finally, this NMR study of Tat Eli in solution constitutes the basis for a future study that will determine the structural changes required for Tat to traverse cellular membranes using solid-state NMR.
Protein synthesis, purification and characterization
The primary sequence of Tat Eli is MDPVDPNLEPWNHPGSQPRTPCNKCHCKKCCYHCPVCFLNKGLGISYGRKKRRQRRGPPQGGQAHQVPIPKQPSSQPRGDPTGPKEQKKKVESEAETDP. Tat Eli was synthesized in solid phase using Fast Fmoc (9-fluoenylmethoxy carbonyl) chemistry by the method of Barany and Merrifield  using 4-hydroxymethyl-phenoxymethyl-copolystyrene-1% divinylbenzene preloaded resin (0.65 mmol) (Perkin Elmer) on an automated synthesizer (ABI 433A, Perkin Elmer) as previously described . Purification was carried out using a Beckman high-pressure liquid chromatography (HPLC) apparatus with a Beckman C8 reverse phase column (10 × 150 mm). Buffer A was water supplemented with 0.1% (v/v) trifluoroacetic acid (Sigma) and buffer B was acetonitrile (Merck) supplemented with 0.1% (v/v) trifluoroacetic acid. Gradient was buffer B from 15–35% in 40 minutes with a 2 ml/min flow rate. HPLC analysis was carried out using a Merck Chromolith™ Performance RP-8e (4.6 × 100 mm) with similar buffers but using a gradient from 10–50% in 15 minutes with a 1.8 ml/min flow rate. Purity of the protein was up to 95%. Amino-acid analyses were performed on a model 6300 Beckman analyzer and mass spectrometry was carried out using an Ettan matrix-assisted laser desorption ionization time-of-flight apparatus (Amersham Biosciences). The synthetic Tat HXB2(86) was previously described . Recombinant Tat was obtained through the NIH AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH from Dr. John Brady and DAIDS, NIAID .
Trans-activation assay with HIV-1 long terminal repeat transfected HeLa cells
The trans-activation activities of the synthetic Tat proteins were analyzed by monitoring the production of β-galactosidase after activation of lacZ expression in HeLa-P4 cells  using a previously described protocol [6, 10]. Briefly, 2 × 105 cells per well were incubated in 24-well flat-bottomed plates (Falcon) at 37°C, 5% CO2, in Dulbecco's Modified Eagles Medium (DMEM) supplemented with 10% (v/v) heat-inactivated fetal bovine serum and 100 μg/ml neomycin (all Invitrogen) After 24 h, cells were washed with phosphate-buffered saline. Tat protein was directly mixed with DMEM supplemented with 0.01% (w/v) protamine (Sigma) and 0.1% (w/v) bovine serum albumin (BSA; Sigma) and added to the cells. After 16 hours at 37°C, 5% CO2, cells were washed with phosphate-buffered saline, lysed and the β-galactosidase content was measured with a commercially available antigen capture enzyme-linked immunosorbent assay (β-galactosidase ELISA, Roche Diagnostics). Results were normalized using the Bradford reagent (Sigma). Control corresponds to the background β-galactosidase expressed by HeLa-P4 cells in DMEM supplemented with 0.01% (w/v) protamine and 0.1% (w/v) BSA with vehicle and without Tat. Concentrations of Tat used are noted in the figure legend.
CD spectra were measured with a 100 μm path length from 260–178 nm at 10–70°C on a JASCO J-810 spectropolarimeter. Data were collected at 0.5 nm intervals using a step auto response procedure (JASCO). CD spectra are presented as Δε per amide. Protein concentration was 1 mg/ml in 20 mM pH 4.5 phosphate buffer for the three proteins: BSA, protamine, and Tat Eli and in 20 mM pH 7 phosphate buffer for Tat Eli with 0 to 16 molar equivalents of ZnCl2. The CD data were analyzed with VARSELEC to determine the secondary structure content according to the method of Manavalan and Johnson  using a set of 32 reference proteins and an average of 4960 calculations.
Tat samples for NMR (1 mM) were prepared in H2O/D2O [9:1] 100 mM phosphate buffer at pH 4.5. The homonuclear 1H NMR spectra were recorded on a Varian Inova 800 MHz NMR spectrometer operating at 799.753 MHz. 1H TOCSY spectra [33, 34] with 80 ms mixing, and NOESY spectra  with 50, 100, 150, and 200 ms mixing, were recorded at 20°C with a spectral width of 10999.588 Hz. The water signal was suppressed using weak presaturation (2 s). Data were processed with the Felix 2002 from Accelrys (San Diego, CA).
Molecular modeling was performed using the Insight II 2002 package including Biopolymer, Discover, Homology and NMR-refine software (Accelrys, San Diego, CA). High temperature simulated annealing was carried out according to Nilges et al. .
We thank Drs Anna S Svane, Anders Malmendal and Niels C. Nielsen for fruitful discussion. We thank Claude Villard and Dr Daniel Lafitte for technical assistance. We acknowledge the Danish Center for NMR of Biological Macromolecules at the Carlsberg Laboratory for the use of the Varian Inova 800 MHz spectrometer. This research was funded by the Conseil Régional Provence Alpes Côte-d'Azur, Conseil Général des Bouches-du-Rhône, Ville de Marseille, Faire Face Au SIDA, the Danish National Research Foundation, The Danish Biotechnological Instrument Centre (DABIC), The Danish Natural Science Council, and Carlsbergfondet. JW has a scholarship from the Conseil Régional Provence Alpes Côte-d'Azur and SynProsis. EPL thanks the Université de la Méditerranée and INSERM for their support of this work.
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