The First Small-Molecule Inhibitors of Members of the Ribonuclease E Family

The Escherichia coli endoribonuclease RNase E is central to the processing and degradation of all types of RNA and as such is a pleotropic regulator of gene expression. It is essential for growth and was one of the first examples of an endonuclease that can recognise the 5′-monophosphorylated ends of RNA thereby increasing the efficiency of many cleavages. Homologues of RNase E can be found in many bacterial families including important pathogens, but no homologues have been identified in humans or animals. RNase E represents a potential target for the development of new antibiotics to combat the growing number of bacteria that are resistant to antibiotics in use currently. Potent small molecule inhibitors that bind the active site of essential enzymes are proving to be a source of potential drug leads and tools to dissect function through chemical genetics. Here we report the use of virtual high-throughput screening to obtain small molecules predicted to bind at sites in the N-terminal catalytic half of RNase E. We show that these compounds are able to bind with specificity and inhibit catalysis of Escherichia coli and Mycobacterium tuberculosis RNase E and also inhibit the activity of RNase G, a paralogue of RNase E.

T he rapid turnover of RNA is central to the regulation of gene expression in all forms of life 1 . It ensures, for example, that translation closely follows programming at the level of transcription. In Escherichia coli, a valuable model system, it has been found that a single-strand-specific endoribonuclease called RNase E is required for rapid turnover of mRNA and in addition the processing of many RNAs including those of the translational machinery 2,3 . E. coli RNase G, a paralogue of RNase E, cooperates with RNase E in the maturation of 16S ribosomal RNA 4,5 and is also involved in the normal degradation of many mRNAs 6,7 . RNase E is a potential target for developing new antibiotics, which are increasingly needed given the rising tide of resistance emerging in bacteria of clinical importance. It is essential for the growth of E. coli 8,9 and homologues have been found in about half of the bacteria whose genomes have been sequenced, including important pathogens, such as Salmonella species, Yersinia pestis, Mycobacterium tuberculosis, and Vibrio cholerae [10][11][12][13] . Furthermore, no homologues of RNase E have been identified in humans or animals.
The N-terminal catalytic half (NTH) of RNase E is a tetramer, which is best described as a dimer of dimers 14,15 . Each dimer contributes a pair of equivalent antiparallel channels that include the sites of catalysis. Each channel binds a single-stranded RNA segment and has an adjacent pocket for binding 59 termini that are both monophosphorylated and unpaired (Fig. 1a-c) 16 . Such termini are found on the downstream products of cleavage and may provide a means of prolonging contact such that additional cleavages can occur 17 . Each single-stranded RNAbinding channel 16 is formed on one side by a domain that closely resembles the RNA-binding domain of S1 18 and on the other side by one that resembles the catalytic domain of DNase I 19 . The latter reveals an unexpected link in the evolution of RNA and DNA nucleases. Aspartic acid residues at 303 and 346 in the DNase I domain may act as general bases to activate the hydroxyl group of a water molecule coordinated to the magnesium to attack the scissile phosphate 16 . The scissile phosphodiester bond in the RNA is the point at which cleavage occurs (the bases 39 to the site of RNA cleavage are defined as 11, 12..., and those 59 are 21, 22...). The contacts between RNase E and bound RNA are described in the legend to Fig. 1a-c. Recent evidence suggests that simultaneous recognition of two or more unpaired regions may provide a sufficiently stable interaction for efficient cleavage by RNase E to occur 6,20,21 . However, it is also clear that the efficient cleavage of some substrates requires them to be 59 monophosphorylated 17,22,23 . A simple explanation for these observations is that because of structural constraints not all RNAs present a combination of unpaired regions that can cooperate in binding RNase E, but for some of these RNAs a 59-monophosphorylated end provides an additional foothold for RNase E that allows binding and cleavage of a co-accessible unpaired region 6,21 .
The study of RNA processing and decay in E. coli has made extensive use of two mutants of RNase E that are temperature sensitive 8,9,24,25 and have amino acid substitutions in the S1-like domain 26 . However, the interpretation of whether specific steps require the endonucleolytic activity of RNase E has been complicated by reports that residual activity is retained at non-permissive temperatures in vivo 27,28 and the observation that for at least one of these mutants aggregation is associated with thermal inactivation in vitro (McDowall, K. J. & Stead, J. A., University of Leeds, unpubl. data). The latter has ramifications because RNase E forms the platform for the assembly of the degradosome complex, which includes other components known to play key roles in RNA processing and turnover 29,30 . Thus, a method of blocking RNase E activity efficiently without consequence on the structural integrity of the degradosome would be of considerable value in assigning cellular functions to RNase E. Although, for the purpose of studying RNA processing and turnover, it is desirable to be able to block RNase E activity in vivo, the ability to do so in cell extracts and preparations of purified components would itself be of considerable value for biochemical studies.
Small molecules that bind within the active sites of essential enzymes have proved to be a source of potent inhibitors and drug leads 31 . In the case of an endoribonuclease, assays can be developed to screen libraries of small molecule inhibitors, that provide a fluorescence output when cleavage of the RNA substrate releases a quencher 32,33 . However, when structure(s) of a target protein is available, such as for RNase E, another option is virtual high-throughput screening (VHTS) 34,35 . VHTS is a computer-based method that provides a score that reflects the likelihood that individual compounds in a library will be able to bind a target receptor 36 . Herein, we report the combined use of SPROUT 37 and eHiTS 38 , VHTS computer packages, to identify small molecules that are predicted to target the NTH of E. coli RNase E. We also report their activity with regard to binding, inhibition and specificity.

Results
Selection of small molecules targeting E. coli NTH-RNase E by VHTS. The site of catalysis and the 59 monophosphate-binding pocket ( Fig. 1b and c) within the single-stranded RNA-binding channel were chosen as targets for VHTS. Two high-resolution Xray crystal structures of E. coli NTH-RNase E as a trapped intermediate with oligoribonucleotide substrates (2BX2 and 2C0B) 16 were first superimposed using SWISS-PDB Viewer 39 . There were no significant differences in the position of amino-acid residues within the chosen targets of the two X-ray structures (data not shown). Thus, we chose arbitrarily to use the coordinates of the 2C0B entry (3.2 Å resolution) for the 59 end-binding pocket and the 2BX2 entry (2.8 Å resolution) for the site of catalysis. Within the CAnGAROO module of SPROUT, the 59 nucleotide of the RNA was used to define a 'cavity' (i.e. the space available for ligand generation) for the 59 monophosphate-binding pocket, while the nucleotides immediately 59 and 39 to the phosphodiester bond that is normally cleaved were used to define a cavity for the site of catalysis. Next, amino acid residues within an envelope that extends 10 Å in radius from the segments of RNA used to derive the cavities were chosen to form the actual receptors for VHTS. 58,833 compounds in the Maybridge database were screened against the '59 monophosphatebinding pocket' and 'catalytic site' receptors using eHiTS. Compounds with an eHiTS score of #24.0 were then analysed further using SPROUT. Those with log p, eHiTS and SPROUT values of #5.0, #24.0 and #24.9, respectively, were viewed -using the SDF file generated by eHiTS -to manually identify those with drug-like properties. The final selection criterion was that compounds should be predicted to form at least one hydrogen bond with RNase E. This was done using the 'Explore' function of the HIPPO module in SPROUT. This produced a list of 23 compounds against the 59 end-binding pocket (designated 'P' compounds) and 10 compounds against the catalytic site (designated 'M' compounds). Of these only 21 and 9 could be supplied commercially to us, respectively (Supplementary Table S1). The predicted docking of small molecules, described further below, into the catalytic site and 59 sensor are provided ( Fig. 1d and e, respectively). An alignment indicating the residues from E. coli RNase E that formed the cavities for docking of small molecules is provided ( Supplementary Fig. S1).
Small molecule binding and inhibition of E. coli NTH-RNase E. The ability of the compounds from VHTS to bind and inhibit a recombinant polypeptide of RNase E, used in previous structural and functional studies [14][15][16]40,41 , was assayed using Surface Plasmon Resonance (SPR) and a discontinuous cleavage assay, respectively. Eleven compounds were found to bind RNase E and are described below. Seven compounds (M3, M5, M8, M9, P6, P11, and P16) produced binding curves consistent with targeting of specific sites, i.e. binding began to plateau at higher concentrations. Of these seven, M5, M8, P6, and P11 clearly inhibited catalysis under the conditions used. Compound M9 also inhibited catalysis but much less efficiently. Three other compounds inhibited RNase E (P10, P14 and P21); however, P10 appeared to bind at sites other than the intended target (i.e. binding did not plateau and was seen to be non-specific), while assaying the binding of P14 and P21 was precluded due to their low solubility. The final compound, M2, did not inhibit RNase E under the conditions used and also appeared to bind but at sites other than the intended target. The SPR and inhibition assay results for M5 and P11, which showed the best inhibition of E. coli RNase E and bind with specificity, are shown along with P10, providing an example of a compound that inhibits but which appears to bind at sites other than the intended target (Fig. 2). Apparent dissociation constants estimated from the SPR experiments, along with nominal IC 50 values are included in Table 1.
Binding and inhibition of Mycobacterium tuberculosis RNase E and E. coli RNase G. A sequence alignment of the catalytic domain of E. coli RNase E with a homologue from M. tuberculosis and RNase G, a paralogue of E. coli RNase E, show high conservation of residues ( Supplementary Fig. S1). The value of compounds that inhibit RNase E, whether as leads for developing new antimicrobials or investigating RNA processing and degradation, is increased if they target homologues in other species as well as the E. coli enzyme. Thus, we assayed the ability of a selection of compounds to bind and inhibit RNase E from M. tuberculosis, a pathogenic bacterial species of significant clinical relevance 42,43 . As found for E. coli RNase E, P11 and M5 produced SPR binding curves consistent with specific targeting (data not shown). Compound P11 showed clear inhibition of M. tuberculosis RNase E, while M5 inhibits activity but appears to be less efficient than with the E. coli enzyme, but most likely reflects the different concentrations of compound used ( Fig. 3a and Fig. 2a). It may also reflect subtle differences in the structure of the active site between the M. tuberculosis and E. coli enzymes and the residues used for docking ( Supplementary Fig. S1).
The compounds shown to inhibit catalysis by E. coli RNase E (P6, P10, P11, M5 and M9) were also found to be able to inhibit the activity of RNase G with comparable IC 50 values ( Fig. 3b and Table 1). The 'P' compounds were slightly less effective with RNase G and, as above, may reflect differences in the 59-monophosphate binding pocket between RNase E and G and in the residues used for docking ( Supplementary Fig. S1). The value of the compounds will be increased further if they can be used in conjunction to target the two different sites (59 sensor and catalytic site) simultaneously to enhance inhibition of RNase E catalysis. When compound M5 (representing targeting of the catalytic site) was incubated with P11 (targeting of the 59 sensor) at their IC 50 concentrations (expect to observe 50% inhibition with the single compound), enhanced inhibition of E. coli RNase E was observed to a level of almost  coli RNase E with bound RNA (green). The dimer is shown as a surface representation with the two protomers superimposed as a cartoon diagram. Red, blue, gold and grey colouring identifies the DNase I, S1, 59 sensor and RNase H domains, respectively. The zinc and magnesium ions are shown as grey and magenta spheres, respectively. (b) The catalytic site. The DNase I side of each of the two channels presents a magnesium ion that is co-ordinated by the carboxylates of aspartic acid residues 303 and 346. The base of the nucleotide at the 12 position relative to the site of RNA cleavage is partitioned into a recess on the surface of the S1 domain. The nucleotide base is held by hydrophobic interactions with a phenylalanine at position 67 and the aliphatic portion of a lysine at position 112. The exocyclic oxygen of the base of the nucleotide immediately 59 forms a hydrogen bond with a lysine at position 106, also in the S1 domain.   (Fig. 4). Whether this enhancement of inhibition is additive or synergistic remains to be determined, but warrants further investigation. To gauge the specificity of inhibition, we found that the compounds shown to inhibit E. coli RNase E catalysis did not inhibit the activity of RNase A, an unrelated ribonuclease (Fig. 5).

Discussion
New and effective antimicrobials are needed to combat the growing number of antibiotic resistant bacteria. The essential enzyme RNase E represents a potential target for the generation of new antimicrobial leads. We have described herein, a method for the selection of small molecule inhibitors against RNase E, which is possible when the structure of the target protein is available. The 59 sensor and the site of catalysis were chosen as targets in the NTH of E. coli RNase E and compounds that were predicted to bind at these sites were selected using VHTS with the combined application of eHiTS 38 and SPROUT 37 . At least some of the selected compounds were shown to specifically bind and inhibit catalysis by E. coli RNase E with K D and IC 50 values in the low millimolar range ( Fig. 2 and Table 1). Furthermore, some of these same compounds can specifically bind and inhibit a homologue from M. tuberculosis and inhibit catalysis by E. coli RNase G, a paralogue of RNase E (Fig. 3), demonstrating a wider application for these compounds. In addition, inhibition of catalysis is specific for the RNase E family (Fig. 5). Although the K D and IC 50 values are relatively high, the approach has been validated and the compounds described here can be used as the starting material for developing better, higher affinity inhibitors. It may also be possible to use them in combination (Fig. 4). The best leads from this study for the development of specific small molecule inhibitors of RNase E would include M5, P6 and P11 (compound M8 became Surface plasmon resonance was used to monitor compound binding to immobilized NTH-RNase E. The concentrations of compound used were 0-2.5 mM for P11, 0-5 mM for M5 and 0-1.5 mM for P10. PBS with 5% DMSO was used as the running buffer. The binding data for each compound concentration at equilibrium is shown (red data points). The steady state fit to the data (black line) gives a K D of ,1.5 mM for P11, ,3 mM for M5 and shows non-specific binding to NTH-RNase E for P10. Compounds P11 and M5 show evidence of beginning to plateau at higher concentrations indicating specific binding, whilst P10 does not.  Table S1), although essentially used in this study as tool compounds in order to probe the ability of small molecules to modulate RNase E function, do indicate the potential 'druggability' of this system in terms of compliance with the Lipinski guidelines for drug likeness. Specifically, they are either sulfonamido (e.g. P6 and P11) or heterocyclic (e.g. M5), and have molecular weights under 500 (e.g. for P6, P11 and M5, molecular weight 5 423, 394, and 420, respectively) with acceptable H-bond donor/acceptor patterns within their structures. The hydrophobic interactions that are usually formed between RNase E and the RNA are mimicked by the inhibitor molecules. For compound M5, the 3-chloro-5-trifluoromethyl pyridine ring is predicted to make hydrophobic interactions with F67 of RNase E and the pyrimidine-2, 4-dione ring is predicted to make hydrophobic interactions with the aliphatic part of K112 analogous to the contacts made to the RNA base immediately 39 to the cleavage site. There is also the possibility of a hydrogen bond between the ester linkage of the acetylcarbamate and the side chain of K106 analogous to the hydrogen bond formed between the exocyclic oxygen of the base of the nucleotide 59 to the cleavage site and K106 (Fig. 1d). The trimethylbenzene ring of compound P11 is predicted to make hydrophobic interactions with V128 analogous to the contacts made to the base of the 59 end nucleotide. There are no obvious hydrogen bonding interactions between RNase E and the tosyl azanecarboxamide group of P11 that are analogous to those formed between T170, R169 and the RNA (Fig. 1e). Modifying this molecule to reintroduce these interactions could improve affinity and inhibition.
In addition to providing leads for new antimicrobials, the inhibitors can be used as part of chemical genetics strategies to dissect the contribution of members of the RNase E family. Finally, the approach described can be extended to identify inhibitors of other families of ribonucleases. For example, it has been recently used in work that will be reported elsewhere to select antibacterials that target 39 to 59 exonucleases.

Methods
Compound-Enzyme inhibition assays. The NTH of E. coli RNase E (residues 1-529) and RNase G were purified as described previously 21,40 . The compounds were obtained from Maybridge and re-suspended in 100% DMSO. Discontinuous cleavage assays were done using a 39 fluorescein-labelled, 59-monophosphorylated version of BR13, a well-characterised substrate of RNase E, with the sequence 59-GGGACAGU#AUUUG 44 . E. coli NTH-RNase E was pre-incubated with and without the compounds at 37uC for 20 min before the addition of substrate in a buffer containing 25 mM Bis-Tris Propane (pH 8.3), 100 mM NaCl, 15 mM MgCl 2 , 0.1% Triton X-100, 1 mM DTT and 20% DMSO. The enzyme monomer and substrate concentrations at the start of the reaction were 0.5 and 62 nM, respectively. The inhibition assays with RNase G and RNase A (Sigma) were carried out as above. Reaction products were analysed by electrophoresis using a denaturing 15% polyacrylamide, sequencing-type gel. Detection was via a FLA-5100 scanner (Fuji). Substrate and product were quantified using AIDA software (Raytest Isotopenmessgerate GmbH). Initial rates of reaction at increasing compound concentrations were obtained by establishing the slope representing percentage product generated over time during the initial, linear phase of the reaction. IC 50 values were calculated by plotting the percentage inhibition of initial rate against compound concentration.
For M. tuberculosis RNase E (a kind gift from Prof. B. Luisi, University of Cambridge), 1 mM 39 fluorescently-labelled, 59 monophosphorylated BR13 was incubated with 50 nM RNase E with and without the compounds in buffer containing 25 mM Tris-HCl (pH 7.5), 100 mM NaCl, 15 mM MgCl 2 , 1 mM DTT and 5% DMSO at room temperature. Reactions were analysed by electrophoresis using denaturing 20% polyacrylamide gels and visualised using a UV transilluminator.
Binding studies by SPR analysis. E. coli and M. tuberculosis RNase E were immobilized covalently using amine coupling to the surface of a Biacore CM5 sensor chip (GE Healthcare). Immobilization levels were approximately 1500 RUs. Assessment of compound binding were conducted by injecting varying compound concentrations in PBS containing 5% DMSO at flow rates of 30-90 ml/min for ,60 s over the reference and test flow cells. A Biacore T100 instrument was used and the data collected was reference and buffer subtracted prior to steady state analysis using data fitting functions provided in the Biacore T100 Evaluation Software. eHiTS and SPROUT. The eHiTS program has been described by Zsoldos et al 38 .
Briefly, eHiTS takes compounds from a library and calculates the optimal conformation each of these ligands can adopt in a cavity of a protein target. The eHiTS approach breaks each ligand into rigid fragments and flexible connecting chains and docks each rigid fragment into every possible place in the cavity. A score is calculated for each structure based upon the geometries of the ligand and the complementarity of surface points on the receptor and ligand: complementary surface points receive a positive score, while repulsive surface points receive a negative score. Other factors are also used to calculate the final score including steric clashes, depth of the cavity, SPROUT 37 is a computer program that generates structures based upon a set of specified constraints. The approach firstly generates a skeleton based upon a set of primary constraints that includes definition of the target site and must satisfy steric and geometric constraints. This is followed by substitution of atoms in the skeleton to generate molecules with the required properties. The CAnGAROO module within SPROUT allows for the definition of potential binding pockets by detecting clefts, defined as a large inward facing area on the surface of the protein. The HIPPO module locates typical donor and acceptor atoms in the protein, intramolecular hydrogen bonds, hydrogen bonding atoms near to the surface of the receptor site and hydrogen bonding regions are computed with tolerances.  conditions and labelling are as Fig. 2a. Lanes numbered 1-3 correspond to samples taken at 0, 5 and 15 min following addition of substrate, respectively. Lane C contains substrate incubated without enzyme for 15 min. Compounds were included in the reactions at their E. coli RNase E IC 50 concentration; 1.9 mM P10, 1.8 mM P11 and 3.8 mM M5 and were included in combination at the same concentrations for M5 with P10 and M5 with P11.
(b) Initial rates were obtained as described in Methods. The initial rate was then normalised to a value of 1 for the reaction containing no compound and represents the product generated in one minute during the initial phase of the reaction. The results are presented as a bar chart.