posted on 2019-11-14, 14:42authored byKhoa N. Pham, Ariel Lewis-Ballester, Syun-Ru Yeh
Indoleamine 2,3-dioxygenase 1 (hIDO1) and tryptophan
dioxygenase
(hTDO) are two of the only three heme-based dioxygenases in humans.
They have recently been identified as key cancer immunotherapeutic
drug targets. While structures of hIDO1 in complex with inhibitors
have been documented, so far there are no structures of hTDO-inhibitor
complexes available. Here we use PF-06840003 (IPD), a hIDO1-selective
inhibitor in clinical trials, as a structural probe to elucidate inhibitor-selectivity
in hIDO1 versus hTDO. Spectroscopic studies show that IPD exhibits
400-fold higher inhibition activity toward hIDO1 with respect to hTDO.
Crystallographic structures reveal that the binding pocket of IPD
in the active site in hIDO1 is much more flexible as compared to that
in hTDO, which offers a molecular explanation for the superior inhibition
activity of IPD in hIDO1 with respect to hTDO. In addition to the
IPD bound in the active site, a second IPD molecule was identified
in an inhibitory site on the proximal side of the heme in hIDO1 and
in an exosite that is ∼40 Å away from the active site
in hTDO. Taken together the data provide new insights into structure-based
design of mono and dual inhibitors targeting hIDO1 and/or hTDO.