Photochemical Probe Identification of a Small‐Molecule Inhibitor Binding Site in Hedgehog Acyltransferase (HHAT)**

Abstract The mammalian membrane‐bound O‐acyltransferase (MBOAT) superfamily is involved in biological processes including growth, development and appetite sensing. MBOATs are attractive drug targets in cancer and obesity; however, information on the binding site and molecular mechanisms underlying small‐molecule inhibition is elusive. This study reports rational development of a photochemical probe to interrogate a novel small‐molecule inhibitor binding site in the human MBOAT Hedgehog acyltransferase (HHAT). Structure‐activity relationship investigation identified single enantiomer IMP‐1575, the most potent HHAT inhibitor reported to‐date, and guided design of photocrosslinking probes that maintained HHAT‐inhibitory potency. Photocrosslinking and proteomic sequencing of HHAT delivered identification of the first small‐molecule binding site in a mammalian MBOAT. Topology and homology data suggested a potential mechanism for HHAT inhibition which was confirmed by kinetic analysis. Our results provide an optimal HHAT tool inhibitor IMP‐1575 (K i=38 nM) and a strategy for mapping small molecule interaction sites in MBOATs.

Abstract: The mammalian membrane-bound O-acyltransferase (MBOAT) superfamily is involved in biological processes including growth, development and appetite sensing. MBOATs are attractive drug targets in cancer and obesity; however, information on the binding site and molecular mechanisms underlying small-molecule inhibition is elusive. This study reports rational development of a photochemical probe to interrogate a novel small-molecule inhibitor binding site in the human MBOAT Hedgehog acyltransferase (HHAT). Structure-activity relationship investigation identified single enantiomer IMP-1575, the most potent HHAT inhibitor reported to-date, and guided design of photocrosslinking probes that maintained HHAT-inhibitory potency. Photocrosslinking and proteomic sequencing of HHAT delivered identification of the first small-molecule binding site in a mammalian MBOAT. Topology and homology data suggested a potential mechanism for HHAT inhibition which was confirmed by kinetic analysis. Our results provide an optimal HHAT tool inhibitor IMP-1575 (K i = 38 nM) and a strategy for mapping small molecule interaction sites in MBOATs.

Members of the membrane-bound O-acyltransferase
(MBOAT) superfamily of proteins are involved in several critically important biological pathways. [1] In humans, these include Wnt acyltransferase (Porcupine; PORCN), [2] Hedgehog acyltransferase (HHAT) [3] and ghrelin O-acyltransferase (GOAT) [4] which regulate Wnt and Hedgehog signaling, and appetite sensing, respectively. These MBOATs are attractive therapeutic targets in cancer and obesity, [1] and structural information for mammalian MBOATs is highly sought after. The membrane topology of various mammalian MBOATs has been experimentally determined, supporting a conserved arrangement of multiple transmembrane helices and catalytic residues. [1a] Recent determination of the structure of a bacterial MBOAT, DltB, provided the first insights into MBOAT architecture and mechanism, [5] revealing that DltB forms a transmembrane pore-like structure with the active site in the centre of the pore, and providing a rationale for how MBOATs can combine substrates present on opposite sides of biological membranes. [5] De novo computational predictions suggest GOAT may adopt a similar structure, [6] and the first cryo-EM structures of a human MBOAT, diacylglycerol O-acyltransferase 1 (DGAT1), [7] confirmed the pore-like architecture of MBOATs and provided insights into the catalytic mechanism. However, the mechanism of small molecule MBOAT inhibition remains largely unknown.
Hedgehog signaling drives growth during development and is reactivated in certain cancers, making HHAT an attractive therapeutic target to block aberrant signaling. [1] HHAT S-acylates Hedgehog signaling proteins, which then undergo S,N-acyl shift to yield the final amide-linked product. [3] HHAT predominantly attaches palmitic (C16:0) fatty acid, using palmitoyl-Coenzyme A (Pal-CoA) as the lipid donor substrate (Figure 1 A). [3] N-acylation of Sonic Hedgehog protein (SHH) by HHAT and C-terminal auto-Ocholesterylation [10] is required for signaling function. We previously determined the membrane topology of HHAT, which consists of ten transmembrane helices, two reentrant loops, and one palmitoylation-tethered reentrant loop (Figure 1 B). [8] Remarkably these experimental analyses undertaken in live cells placed the MBOAT signature residues His379 and Asp339 on opposite sides of the membrane, raising questions regarding the potential role of these residues in the catalytic mechanism. There is one known series of small-molecule inhibitors of HHAT, [11] with RUSKI-201 (1, Figure 1 C) the only molecule in this class with proven ontarget cellular activity over a non-cytotoxic concentration range. [9] 1 contains two undefined stereocenters, with further scope for exploration of the structure-activity relationship (SAR) to generate higher potency inhibitors. There is also currently no information about this series binding mode at HHAT, or indeed the binding site of any inhibitor of a mammalian MBOAT. Photocrosslinking of ligands to proteins followed by proteomic mass spectrometry-based sequencing is a powerful method to identify binding sites. [12] However, mass spectrometry studies remain technically challenging for integral membrane proteins. [13] Here, we report a SAR investigation leading to discovery of the most potent single-enantiomer HHAT inhibitor to date, and rational design of a photochemical probe that was applied to identify the small-molecule inhibitor binding site in HHAT, providing the first insights into the mechanism of HHAT inhibition.
The amide-linked side chain of 1 was selected for SAR investigation. The 4,5,6,7-tetrahydrothieno[3,2-c]pyridine core (2) was synthesized by Bischler-Napieralski cyclization, [14] or via a shorter and higher yielding Pictet-Spengler cyclization (Scheme S1). Acetylated derivative 3 was prepared to investigate the importance of the aminoalkyl chain. Amide-linked sidechain derivatives 4-6 were prepared via Nbenzyl-protected intermediates to enhance handling of the amines by decreasing volatility (Scheme S2). 1 contains two undefined stereocenters, in the central ring system and in the 2-methylbutylamino chain. To investigate the stereochemical requirements for inhibition, (S)-2-methylbutylamine was used to prepare 4 with defined sidechain stereochemistry. 3-Methylbutylamine (5) and 2-methylpropylamine (6) derivatives were prepared to remove the stereocenter. To investigate the importance of the sidechain secondary amine, tertiary amine 7 and cyclic derivative 8 were prepared from N-methyl isobutylamine and 3-methyl piperidine, respectively. To further probe the role of the secondary amine, urea derivative 9 was prepared from isopentylamine (Scheme S2).
Collectively, SAR data demonstrated the amide carbonyl was critical for HHAT binding, whereas the secondary amine improved potency but was not essential and alteration of the alkyl chain was well-tolerated. These new insights led to design of photocrosslinking chemical probes 10 and 11 to investigate the small-molecule binding site in HHAT (Figure 2 A). In probe 10 the secondary amine moiety was exchanged for a diazirine group, and the terminal alkyl chain replaced with an alkyne; probe 11 contains an additional carbon between the carbonyl and diazirine. The diazirine allows photoactivated chemical crosslinking to nearby residues in HHAT, with the alkyne allowing biorthog-onal functionalization via copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC, "click chemistry") for subsequent analysis. In silico SAR analysis using the inhibitory potency of compounds 1-9 as a training set predicted both probes to be active HHAT inhibitors ( Figure S6). The sidechains were synthesized and coupled to 2 (Scheme S4,5). Pleasingly, probes 10 and 11 retained inhibitory activity against HHAT (IC 50 = 16 mM, 95 % CI = 12-20 mM and IC 50 = 2.4 mM, 95 % CI = 1.8-3.3 mM, respectively, Figure 2 B) demonstrating the key functional groups were tolerated. Probe photoactivation by UV irradiation (365 nm) was monitored by LC/MS, demonstrating an activation half-life of 3.3 min for probe 10 and 32 s for 11 ( Figure S7). Protein crosslinking was next investigated through CuAAC functionalization with a fluorophore and in-gel fluorescence readout. As an integral membrane protein, HHAT presents substantial challenges in sample handling and cannot be precipitated to remove excess fluorophore which otherwise binds non-specifically (data not shown). Fluorogenic azide CalFluor-647 (Figure S8) [18] was therefore used to reduce background fluorescence from dye that had not reacted with alkyne probe. 10 or 11 (10 mM) were incubated with purified HHAT with or without UV irradiation (1 min). Functionalization with Cal-Fluor-647 by CuAAC followed by in-gel fluorescence analysis indicated crosslinking of probe 11 to HHAT promoted by UV irradiation (Figure 2 C), whereas probe 10 showed minimal crosslinking under these conditions ( Figure S8). Competing probe 11 binding with 40-fold excess IMP-1575 reduced crosslinking to near background levels (Figure 2 C).
Having identified suitable conditions for photocrosslinking of 11 to HHAT, identification of the small-molecule binding site was sought through crosslinking with protease digestion and tandem LC-MS/MS analysis. To achieve maximum sequence coverage purified HHAT (1 mg) was digested with trypsin, Glu-C, Proteinase K, chymotrypsin, combinations of Lys-C and trypsin, or ProteaseMAX and trypsin. Filter-aided sample preparation (FASP) [19] was used to remove n-dodecyl-b-D-maltopyranoside (DDM) detergent used to solubilized HHAT, and reduce and alkylate peptides prior to analysis. Moderate-to-low sequence coverage was achieved with all proteases (Table S1), with chymotrypsin having greatest coverage (51 %). Combined, chymotrypsin, Proteinase K (41 %), and trypsin (35 %) gave 68 % overall sequence coverage ( Figure S9). Purified HHAT and 11 (25 mM) were irradiated for 3 min, followed by FASP processing and digestion with trypsin, chymotrypsin, or Proteinase K. LC-MS/MS identified two peptides with increased mass consistent with crosslinking to 11, and MS/ MS fragmentation indicated modification of residues Pro212, Val213, His215, Glu399 and Val402 ( Figure S10). Aliphatic diazirines have a general preference for crosslinking to larger polar amino acids, [20] indicating the probe-modified residues detected in HHAT may be directed by specific interactions with 11.
which is positioned near the cytosolic face of the membrane, or immediately following transmembrane helix 8 (Glu399 and Val402), which is also positioned on the cytosolic membrane face. These residues are distant in the HHAT primary sequence from the signature MBOAT catalytic residues (Asp339 and His379), therefore a structural model for HHAT was generated based on sequence homology to DltB [5] (Figure 2 E). Phyre2, SwissModel and Robetta (old and new) servers were used to generate homology models of HHAT. Models were initially screened based on agreement with previous topology data. [8] Interestingly, all models shared the same fold between residues 94-206, with greater variability in the final two predicted transmembrane helices at the N-and C-termini. A final model was selected based on optimal hydrophobic packing of the terminal membranespanning helices (Figure 2 E). Predicted transmembrane regions from topology studies were arranged around a central pore (Figure 2 E, shown in grey). Signature MBOAT His379 was located at the center of the pore in close proximity to the catalytically essential Asp339, suggesting a central catalytic site. Inhibitor-binding residues Pro212, Val213, and His215 were located adjacent to the proposed catalytic site, whereas residues Glu399 and Val402 were not located in proximity to the proposed catalytic site in this model (Figure 2 E).
Collectively, this analysis suggested that there may be a small-molecule inhibitor-binding site in HHAT located on the cytosolic side of the ER membrane in proximity to the catalytic site. As Pal-CoA is expected to approach HHAT from the cytosolic side of the membrane, this suggested compounds from this series, such as IMP-1575 (Figure 3 A), may bind in competition with Pal-CoA. IMP-1575 (50-0.023 mM) was therefore analyzed for effects on HHAT kinetics at varying Pal-CoA concentrations (50-0.19 mM, Figure 3 B,C). Analysis using a mixed model equation for inhibition [21] generated a = 470 (95 % CI = 320-620), indicative of a competitive mode of inhibition for IMP-1575 with respect to Pal-CoA (K i = 38 nM, 95 % CI = 29-46 nM). Taken together, these data support identification of a small-molecule binding site in HHAT that competes with Pal-CoA binding to disrupt enzymatic function with high affinity.
We present here a new paradigm in rational development of photocrosslinking chemical probes for MBOATs that can identify small-molecule binding sites on these very challenging but important targets. Probe 11 was designed based on new SAR insights into known inhibitor 1, which retained required HHAT inhibitory activity (Figure 2). Probe 11 was used here to identify a small-molecule inhibitor binding site in an MBOAT for the first time. Other mammalian MBOATs, such as PORCN and GOAT, have known inhibitors and their investigation may be expedited by technical advancements reported here, including use of fluorogenic click regents for SDS-PAGE analysis, and FASP processing in combination with multiple proteases to increase sequence coverage. Photochemical tools based on substrates may further allow mapping of key functional sites in HHAT and other MBOATs. The limitations of biochemical topology analysis and homology models for inhibitor design are significant, therefore direct structural information for MBOATs remains an important goal for future inhibitor development. We further disclose IMP-1575, a single enantiomer small molecule, as the most potent HHAT inhibitor reported to date that competes with Pal-CoA (K i = 38 nM, Figure 3). Previous studies of this chemical series suggested it is noncompetitive with Pal-CoA (for RUSKI-43, K i = 6.9 mM); [11] however, these experiments did not test inhibitor concentrations below 10 mM, preventing accurate mechanistic determination. Future studies of HHAT enzymology could take advantage of IMP-1575, with the inactive enantiomer serving as an ideal control. In this regard, the improved synthetic routes to HHAT inhibitors (Schemes S1-3) presented here will significantly accelerate future development of this series. In summary, we present chemical tools and methodology to provide insight into HHAT which may expedite future studies and drug discovery efforts against this important target class.