User:Demétrio Speckhort/Sandbox 1

The SPPV14

The elimination of infected cells through programmed cell death (apoptosis) is the most common response against infectious agents, acting as a primary defense mechanism. In order to prevail in face of such mechanisms, several viruses express inhibitors that prevent apoptosis, combating the host's innate defenses. Sheeppox virus expresses SPPV14, an inhibitor that intervenes in the pro- or anti-apoptotic pathways mediated by the Bcl-2 protein family, exhibiting a high inhibitory capacity for apoptosis in virus-infected cells. Unlike most viral strategies, which target the production of Bcl-2 homologs (anti-apoptotic)^[1], SPPV14 is a potent inhibitor of Hrk, Bax and Bak (pro-apoptotic)^[2]. This protein shares high similarity with DPV022 (deerpox), which is structurally the closest to SPPV14.

Structure and Function

In the crystal structures of SPPV14 bound to BH3 peptide motifs, it is observed that SPPV14 is a monomeric structure. The possibility of it being a homodimer in a cellular context cannot be excluded, but the data show that its active form is monomeric. SPPV14 is a prosurvival protein that utilizes the canonical ligand-binding grove to engage BH3 motif peptides of proapoptotic Bcl-2 proteins^[2]. binds to through specific interactions, which are essential for the formation of the heterodimeric complex AB between SPPV14 and the BH3 peptide.

SPPV14 has a globular form, consisting of a surrounded by , thus forming the classical structure and fold of Bcl-2. The canonical binding site of SPPV14 is formed by the Ⲁ2-Ⲁ5 helices. The action of the SPPV14 is by sequestering BH3-only proteins including Bim, Bid, Bmf, Hrk, and Puma as well as Bak and Bax; SPPV14 strongly binds with Hrk and Bax, and the interactions are primarily mediated by the 4 hydrophobic canonical sites present in SPPV14, as well as numerous ionic interactions and hydrogen bonds. Unlike other vBcl-2, SPPV14 forms or with Bax D68, reminiscent of a highly conserved ionic bond between Arg in the BH1 region, pro-survival motif of mammals, and the Bcl-2 protein that retains the Asp of the functional BH3 motif^[1].

Interactions with Bax

The interaction between SPPV14 and Bax relies on hydrophobic interactions as well as hydrogen bonds. The conserved hydrophobic residues fit into the corresponding four hydrophobic pockets of the SPPV14-binding groove. Moreover, the Bax residue (in pink) occupies a fifth pocket formed by residues C38, V41, I42, F133, and N137 (in blue) of SPPV14-binding groove, in addition to the four canonical hydrophobic residues. between the hydroxyl (OH-) group of SPPV14 S81 and the lysyl group ((CH2)4NH2) of Bax K64 are also observed, between the main chain carbonyl (in grey) of SPPV14 I74 and the hydroxyl group (highlight in red) of Bax S60^[2]. The interaction between SPPV14 and Bax relies on hydrophobic interactions as well as hydrogen bonds. The conserved hydrophobic residues L59, L63, I66, and L70 from Bax fit into the corresponding four hydrophobic pockets of the SPPV14-binding groove. Moreover, the Bax residue M74 occupies a fifth pocket formed by residues C38, V41, I42, F133, and N137 of SPPV14-binding groove, in addition to the four canonical hydrophobic residues. Hydrogen bonds between the hydroxyl group of SPPV14 S81 and the lysyl group of Bax K64 are also observed, as well as between the main chain carbonyl of SPPV14 I74 and the hydroxyl group of Bax S60.