ToxT

The crystal structure of ToxT is resolved in monomeric form, after isolation from Vibrio cholerae strain O395.

Introduction

ToxT is a molecule at the end of a transcriptional cascade that autoregulates the transcription of the primary virulence factors of Vibrio cholerae[3] and itself. ToxT is a cytoplasmic protein that is activated in turn by ToxR, which is itself activated by ToxS in response to environmental stimuli. These two factors, cholera toxin (CT)[4] and the toxin co-regulated pilus (TCP), are instrumental in causing the disease cholera[5]. This is an intestinal infection resulting in massive water loss in the affected individual, causing extreme dehydration.[6]

spinqualitylabelsall models ToxT, 1.9 Angstrom resolution crystal structure Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural Features DNA-binding. ToxT belongs to a family of transcriptional regulators headed by and known as AraC. The AraC family is characterized by a 100 amino acid region of sequence similarity that forms a DNA-binding domain with two helix-turn-helix motifs (one on either side of the black linker). The two HTH regions are linked by a very polar alpha helix (shown in black). The overall domain is located at the C-terminus. Assuming ToxT is similar in mechanism to other AraC proteins, helix six from HTH1 and helix nine from HTH2 become aligned with the help of helix seven (the polar linking region) to allow binding to major consecutive grooves of target DNA (specific promoters for virulence genes).[1]. The conformation of helix seven is dependent on the ligand bound. Ligand-binding. A nine-stranded beta sheet sandwich or "jelly-roll" with three other alpha helices (overall making up the N-terminus) contain a binding pocket. This is made from several residues from the N-terminus (Y12, Y20, F22, L25, I27, K31, F33, L61, F69, L71, V81, and V83), and a few from the C-terminus (I226, K230, M259, V261, Y266, and M269). The pocket is highly hydrophobic, and has a known volume of 780.9 Angstroms. This pocket contains a ligand: cis-palmitoleate which appears to have a negative effect on virulence when present in vitro. The cis-palmitoleate forms salt bridges with residues K31 and K230 (for detail, see Figure 1B of: [2]). This unsaturated fatty acid, like other UFAs,[3] tend to inhibit genes under the control of ToxT. Specifically, the cis-palmitoleate (PAM) appears to change ToxT's conformation, and thus lower its ability to bind DNA and form dimers. The presence of UFAs is associated with being in the lumen of the intestine during the bacterial infection. PAM brings K31 and K230 together from either end of the protein, and essentially closes off ToxT. K230 is at the end of helix seven, and binding to K31 causes helix six to be pulled into an unfavorable conformation that deters DNA binding. In lower concentration of fatty acids, ie: after penetrating the intestine's mucus, PAM is in lower concentration and tends subsequently not to be bound, and the two lysine residues repel each other to give ToxT an open conformation. The freedom of helices six and seven to find a favorable configuration allows DNA binding to occur. Dimerization. Though the structure shown is a monomer with two overall domains (N-terminal and C-terminal), ToxT tends to form a dimer. The preferred state of ToxT varies between promoters, but binding to the ctx promoter to generate cholera toxin appears to be possible only in the dimer form.ToxT binds to thirteen base pair sequences (can be single, direct, or inverted repeats) called toxboxes in order to activate their respective promoters.[4] Ligand In this resolved structure, cis-palmitoleate[5] is shown, which can be bound in the beta sheet barrel (as discussed above). This unsaturated fatty acid reduces virulence expression in Vibrio cholerae.

Further Study

Conclusive results about what activates ToxT itself has not yet been found. The varying activity of ToxT dependent on the presence of cis-palmitoleate or other unsaturated fatty acids represents a detailed method of effective pathogenicity in humans, but may not be a reasonable target for drug treatment. By restricting transcription (and thus translation and protein production) of virulence genes until the bacterium is determined to be in a favorable location for infection, Vibrio cholerae avoids wasting energy producing virulence factors that will just be cleared by the intestine. This is a specific mechanism to ensure that the bacterium also injects CT and TCP where they will do the most damage, perpetuating the infection.

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Ingrid Youngworth, Yang Yang, Michal Harel, Jaime Prilusky, Alexander Berchansky