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New Noncovalent Inhibitors of Penicillin-Binding Proteins from Penicillin-Resistant Bacteria

  • Samo Turk ,

    Contributed equally to this work with: Samo Turk, Olivier Verlaine

    Affiliation Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia

  • Olivier Verlaine ,

    Contributed equally to this work with: Samo Turk, Olivier Verlaine

    Affiliation Centre for Protein Engineering, University of Liège, Liège, Belgium

  • Thomas Gerards,

    Affiliation Laboratory of Organic Chemistry, University of Liège, Liège, Belgium

  • Matej Živec,

    Affiliation Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia

  • Jan Humljan,

    Current address: Lek Pharmaceuticals d.d., Mengeš, Slovenia

    Affiliations Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia, Lek Pharmaceuticals d.d., Mengeš, Slovenia

  • Izidor Sosič,

    Affiliation Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia

  • Ana Amoroso,

    Affiliation Centre for Protein Engineering, University of Liège, Liège, Belgium

  • Astrid Zervosen,

    Affiliation Laboratory of Organic Chemistry, University of Liège, Liège, Belgium

  • André Luxen,

    Affiliation Laboratory of Organic Chemistry, University of Liège, Liège, Belgium

  • Bernard Joris,

    Affiliation Centre for Protein Engineering, University of Liège, Liège, Belgium

  • Stanislav Gobec

    Affiliation Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia

New Noncovalent Inhibitors of Penicillin-Binding Proteins from Penicillin-Resistant Bacteria

  • Samo Turk, 
  • Olivier Verlaine, 
  • Thomas Gerards, 
  • Matej Živec, 
  • Jan Humljan, 
  • Izidor Sosič, 
  • Ana Amoroso, 
  • Astrid Zervosen, 
  • André Luxen, 
  • Bernard Joris



Penicillin-binding proteins (PBPs) are well known and validated targets for antibacterial therapy. The most important clinically used inhibitors of PBPs β-lactams inhibit transpeptidase activity of PBPs by forming a covalent penicilloyl-enzyme complex that blocks the normal transpeptidation reaction; this finally results in bacterial death. In some resistant bacteria the resistance is acquired by active-site distortion of PBPs, which lowers their acylation efficiency for β-lactams. To address this problem we focused our attention to discovery of novel noncovalent inhibitors of PBPs.

Methodology/Principal Findings

Our in-house bank of compounds was screened for inhibition of three PBPs from resistant bacteria: PBP2a from Methicillin-resistant Staphylococcus aureus (MRSA), PBP2x from Streptococcus pneumoniae strain 5204, and PBP5fm from Enterococcus faecium strain D63r. Initial hit inhibitor obtained by screening was then used as a starting point for computational similarity searching for structurally related compounds and several new noncovalent inhibitors were discovered. Two compounds had promising inhibitory activities of both PBP2a and PBP2x 5204, and good in-vitro antibacterial activities against a panel of Gram-positive bacterial strains.


We found new noncovalent inhibitors of PBPs which represent important starting points for development of more potent inhibitors of PBPs that can target penicillin-resistant bacteria.


β-lactams (penicillins, cephalosporins and carbapenems) are the most widely used antibiotics, due to their high effectiveness, low cost, ease of use, and minimal side effects. At the molecular level, β-lactams target the transpeptidase activity of penicillin-binding proteins (PBPs) that are involved in bacterial cell-wall biosynthesis[1]. In the presence of these antibiotics, the PBPs form a lethal covalent penicilloyl-enzyme complex that blocks the normal transpeptidation reaction; this finally results in bacterial death. However, Gram-negative bacteria have acquired resistance to β-lactams mainly through three different strategies: production of a specific β-lactam hydrolase (the wide-spread β-lactamases); presence of low-affinity PBPs; and active expulsion of β-lactams via efflux pumps[2]. There is thus an urgent need to develop new antibiotics to overcome the challenge of bacterial resistance to existing antimicrobials.

Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of hospital- and community-acquired bacterial infection, and is a global health threat[3], [4]. Methicillin resistance in MRSA strains has arisen from acquisition of the mecA gene, which encodes a novel β-lactam-insensitive PBP (PBP2a)[5]. The crystal structure of PBP2a in both its apo form and complexed to β-lactams has shown that methicillin resistance is achieved through a distorted active site, which requires an energetically costly β3 strand movement to allow acylation by β-lactam antibiotics[6]. One of the possibilities to overcome this intrinsic poor acylation efficiency of PBP2a is to design new β-lactams that have improved binding affinities due to increased noncovalent interactions between the inhibitor and the active site. On the other hand, noncovalent compounds that bind tightly to the active site without acylation might also provide highly effective inhibitors. Noncovalent inhibitors will not require the unfavorable conformational changes in the active site of PBP2a that are required for acylation, and they will hopefully also not be susceptible to β-lactamases[1], [6]. To date, only a few noncovalent inhibitors of PBPs have been described[7][9], and so we screened our in-house bank of compounds for potential inhibition of this important drug target.

Results and Discussion

Screening with a series of more than 250 compounds belonging to different nonreactive chemical classes allowed us to identify an initial hit in compound 1 (Figure 1), which inhibited PBP2a with a promising IC50 of 97 µM (Table 1). To obtain a small focused library of structurally related compounds for further studies, computational similarity searches were performed based on the structure of compound 1 as a starting point and using the ChemBridge bank of compounds. The ZINC[10] built-in search engine together with Ftrees 1.0 (BioSolveIT GmbH) software[11] was used. Two different queries were used (query A (compound 1) and query B, Figure 2) and Tanimoto similarity coefficient was set to 0.90. The only difference between the queries is the bond linking naphthalene ring with anthranilic acid: sulfonamide in query A is replaced with an amide in query B. From the hits of similarity search we selected only the compounds with unprotected functional groups. Similarity search with FTrees gave compounds 2 and 3 while the rest were obtained by similarity search with ZINC built-in search engine (Figure 1).

Additionally to screening on PBP2a, all of these compounds were also evaluated for inhibition of two other PBPs: PBP2x from the highly drug-resistant Streptococcus pneumoniae strain 5204[12], and PBP5fm from the drug-resistant Enterococcus faecium strain D63r (Table 1) [13]. All three of the enzymes used for screening are resistant PBPs from important human-pathogen species that are related to community and nosocomial infections, and that therefore represent important drug targets. Similar to PBP2a, resistance to penicillin in PBP2x 5204 and PBP5fm is acquired by active-site distortion, which lowers their acylation efficiency for β-lactams.

All of these compounds were evaluated biochemically in the presence of detergent (Triton X-100), to exclude the formation of detergent-sensitive promiscuous aggregates[14]. Identical results were observed after 30 or 240 minutes of pre-incubation of the enzyme with the compounds, suggesting rapid and noncovalent inhibition. For the compounds that inhibited at least one of the enzymes under investigation, in-vitro antibacterial activity was determined using a panel of five Gram-negative and 15 Gram-positive bacterial strains (Table 2).

Table 2. In-vitro antibacterial activities of inhibitors of PBPs from resistant species.

As with PBP2a, compound 1 inhibited PBP2x 5204 with an IC50 value of 391 µM. The importance of this hit compound is further underlined by its very promising minimum inhibitory concentrations (MICs) against several Gram-positive bacterial strains, including MRSA (32 µg/mL). Indeed, this MIC value for all of the Staphylococcus aureus tested strains (32 µg/ml or 80 µM) is lower than the IC50 value observed for PBP2a (97 µM), suggesting that in vivo compound 1 does not only inhibit PBP2a but could be active on other different cellular targets. This assumption is confirmed by the fact that for S. aureus ATCC25923 strain, sensitive to penicillin and devoid of PBP2a, compound 1 has the same MIC value as for the other two resistant S. aureus strains (Table 2) where PBP2a is present. To better understand the antibacterial activity of compound 1, we performed an experiment to evaluate the effect of compound 1 on the protoplasts of S. aureus ATCC43300 resistant strain, at a concentration equivalent to 4 times the MIC. After ten minutes, the complete lysis of protoplasts was observed, strongly suggesting an effect of compound 1 on S. aureus plasma membranes. Furthermore, killing curves experiments, at equivalent concentration of compound 1, showed an immediate decrease in the bacterial count, and no viable cells were observed after 120 min, showing a fast bactericidal effect (data not shown) presumably not solely related to the inactivation of PBPs. This suggests that compound 1 may trigger additional cellular events which positively contribute to the antibacterial activity. Further analysis is needed to better understand the precise mode of action of these inhibitors on the bacterial cell.

From the series of sulfonamide compounds 2–5, the only inhibitor was the quinoline-8-sulfonamide derivative compound 2, which inhibited PBP5fm. Although the IC50 was moderate and compound 2 did not have significant antibacterial activity (MICs above 512 µg/mL), it represents a very important hit compound, as to the best of our knowledge, this is the first noncovalent inhibitor of PBP5fm to be described. Promising inhibitors were also seen in the series of anthranilic acid derivatives, compounds 6–12. 5-Bromo-2-(4-propoxybenzamido) benzoic acid, compound 6, was a good inhibitor of PBP2a (IC50, 210 µM) with lower inhibition seen for the other two enzymes, and a generally good in-vitro antimicrobial activity against Gram-positive bacteria, even if its growth inhibition of MRSA strains was only moderate. If the 5-bromo substituent was replaced by a 5-hydroxy group or removed, the enzyme inhibitory activity of compounds 7 and 8, respectively, significantly decreased. In compounds 9–12, the propoxy-substituent of the benzamido part of the inhibitors is at position 3. 5-Bromo-2-(3-propoxybenzamido)benzoic acid, compound 9, was a very promising inhibitor of both PBP2a and PBP2x 5204 (IC50, 230 µM and 155 µM, respectively). Also, compound 9 showed good antibacterial activity against Gram-positive bacterial strains, and in particular against E. faecium and S. pneumoniae, as well as both sensitive and resistant S. aureus. If the 5-bromo substituent was replaced by a methyl, compound 10, inhibition of PBP2a was reduced three-fold and inhibition of PBP2x 5204 was lost.

Consequently, the antibacterial activity of compound 10 decreased for all of the bacteria, with the exception of pneumococcal strains, where surprisingly it remained unchanged. Introduction of the hydroxyl group to position 5 in compound 11 further reduced the PBP inhibitory activity. The 5-unsubstituted anthranilic acid derivative compound 12 was a moderate inhibitor of PBP2a and PBP5fm (IC50, 910 µM and >1 mM, respectively). The MICs were also consistent with poor PBP inhibitory activity, as they were not better than 256 µg/mL for all of the bacterial strains under investigation.

To hypothesize the binding modes of the two best inhibitors, which could assist further structural optimization, inhibitors 1 and 9 were docked into the active sites of PBP2a (pdb code 1VQQ) and PBP2x, respectively. Since there is no known crystal structure of PBP2x 5204, the coordinates of the structurally related (97% sequence identity, Figure 3) PBP2x Sp328 (pdb code 1K25) were used as a template for building the model of PBP2x 5204. Sybyl 8.0 (Tripos Inc.) was used to replace amino acid residues that differ between PBP2x Sp328 and PBP2x 5204. The homology built model was then minimized so that there were no clashes between side chains of the protein.

Figure 3. Sequence identity between PBP2x Sp328 and PBP2x 5204.

PBP2x Sp328 and PBP2x 5204 show high sequence identity with differences in only few places.

The docking study was performed using FlexX 3.0[15]. The PBP2a active site contains a nucleophilic Ser403, while the backbone nitrogens of Ser403 and Thr600 form a conserved oxyanion hole, and Lys406 functions as a catalytic base[6]. These data were used to define the size and position of the active-site pocket in the docking experiments. The active site was defined as the area within 10 Å from Lys406. Figure 4 shows the predicted binding conformation of inhibitor 1 in the active site of PBP2a. Inhibitor 1 forms interactions with amino acids that have previously been shown to be important for the binding of the substrate[6]. The sulfonamide oxygen forms H-bonds with Thr600, while the anthranilic acid phenyl ring binds to Lys406 through π-cation interactions. The naphthalene ring forms hydrophobic interactions with Met641 and Tyr446 (not shown, for clarity).

Figure 4. Docking of the sulfonamide inhibitor 1.

Inhibitor 1 (magenta) docked into the active site of PBP2a (pdb code 1vqq). The amino acids that form interactions with inhibitor 1 are shown as green sticks.

Similarly, PBP2x 5204 also contains a nucleophilic serine (Ser337) in its active site, as well as two lysines (Lys340 and Lys547) that can act as a catalytic base[16]. Active site was defined as the area within 10 Å from Lys340. Figure 5 shows the predicted binding conformation of inhibitor 9 in the active site of PBP2x 5204. At least two H-bonds are possible: Ser337 and Asn397 form H-bonds with the inhibitor 9 amide oxygen and nitrogen, respectively. Both of the lysines of the active site form interactions with the free carboxylic group of inhibitor 9. The binding affinity here might be improved by introducing substituents to the position 5 of the anthranilic acid ring. For example, the bulky bromine can be substituted by larger hydrophobic groups, such as isopropyl or tert-butyl. In addition, by comparing the activity of compounds 6 and 9, which differ only in the position of the propyloxy substituents, we can postulate that the proper position of this substituent on benzoic acid ring appears to be position 3. This is in agreement with our docking study, where unfavorable steric clashes of 4-propyloxy group with the active site of PBP2x 5204 are possible in the case of the compound 6.

Figure 5. Docking of the anthranilic acid derivative inhibitor 9.

Inhibitor 9 (magenta) docked into the active site of PBP2x 5204. The amino acids that form interactions with inhibitor 9 are shown as green sticks.

In conclusion, this screening of our in-house bank of compounds followed by similarity searches performed on the ChemBridge databank containing more than 800,000 compounds has led to the identification of new noncovalent inhibitors of PBPs (PBP2a, PBP2x 5204 and PBP5fm) from the penicillin-resistant bacterial strains. Inhibitors 1 and 9 are shown to have promising inhibitory activities of both PBP2a and PBP2x 5204, and good in-vitro antibacterial activities against a panel of Gram-positive bacterial strains. Therefore, inhibitors 1 and 9 represent important starting points for synthetic modifications and development into more potent noncovalent inhibitors of PBPs that can target penicillin-resistant bacteria.

Materials and Methods


Computational part was done on workstation with 4 dual core AMD Opteron 2,0 GHz processors, 16 GB of RAM, 4 320 GB hard drives in RAID10 array and nVidia GeForce 7900 graphic card. Workstation has Fedora 7 64 bit installed.

Similarity searching was done with ZINC [10] built-in engine and with FTrees 1.0 (BioSolveIT GmbH) [11]. Queries A and B were used with both search engines. In all cases ChemBridge bank of compounds was used and Tanimoto similarity coefficient was set to 0.90. Additionally Dynamic Match Search and Global Gap Penalty were user for FTrees search.

Homology building was done with Sybyl 8.0 (Tripos Inc.). Coordinates of PBP2x Sp328 (pdb code 1K25) were used as a template for building the model of PBP2x 5204. Amino acid residues that differ between the two PBPs were replaced. Replaced amino acids were then minimized using Tripos Force Field.

Docking was done with FlexX 3.0 (BioSolveIT GmbH)[15]. For docking in PBP2a we used crystal structure 1VQQ and for docking in PBP2x 5204 we used our homology built model. Active site was defined as the area within 10 Å from Lys406 and Lys340 for PBP2a and PBP2x 5204 respectively. Docking parameters were the same in both cases. For base placement Triangle Matching was used and the program generated maximally 200 solutions per iteration and 200 per fragmentation.



Chemicals were from Sigma-Aldrich and Acros Organics, and were used without further purification. Solvents were used without purification or drying, unless otherwise stated. Analytical TLC was performed on Merck silica gel (60F254) plates (0.25 mm), and the compounds were visualized with ultraviolet light. Column chromatography was carried out on silica gel 60 (particle size, 240–400 mesh). Melting points were determined on a Reichert hot-stage microscope and are uncorrected. 1H-NMR spectra were recorded on a Bruker AVANCE DPX300 spectrometer in CDCl3 or DMSO-d6 solution, with TMS as the internal standard. IR spectra were obtained on a Perkin-Elmer 1600 FT-IR spectrometer. Microanalyses were performed on a Perkin-Elmer C, H, N analyzer 240 C. Mass spectra were obtained using a VG-Analytical Autospec Q mass spectrometer.

Synthesis of compound 1.

6-Butoxynaphthalenesulfonyl chloride 14 was prepared according to the three-step procedure previously described (Scheme 1)[17]. In the next step it was coupled with methyl anthranilate to give sulfonamide 15. The target compound 1 was obtained after the final hydrolysis with 1 M NaOH/dioxane (Figure 6).

Procedure for the preparation of methyl 2-(6-butoxynaphthalene-2-sulfonamido)benzoate (15).

To an ice-cold solution of methyl anthranilate (2.04 mmol, 309.4 mg) in dry CH2Cl2 (5 mL), Et3N (2.5 mmol, 505 mg) and a solution of compound 14 (1.0 mmol, 597.0 mg) in CH2Cl2 (5 mL) were slowly added. The reaction mixture was stirred at 0°C for 30 min and then at room temperature for 24 h. After the reaction was complete (monitored by TLC), 1 M HCl (15 mL) was added and the mixture extracted with CH2Cl2 (3×20 mL). The combined organic layers were washed with brine (2×30 mL), dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (EtOAc-hexane = 1/3), to provide a white solid, 310 mg (75%), which was immediately used in the next step.

Procedure for the preparation of 2-(6-butoxynaphthalene-2-sulfonamido)benzoic acid (1).

To a stirred solution of 15 (0.60 mmol, 250.0 mg) in dioxane (5 mL), 1 M NaOH (3 mL) was slowly added, and the reaction mixture stirred overnight at room temperature. Then the reaction mixture was diluted with H2O (20 mL) and washed with EtOAc (3×20 mL). The aqueous phase was acidified with 1 M HCl to pH 1, and extracted with EtOAc (3×20 mL). The combined organic layers were washed with brine (2×30 mL), dried over Na2SO4, filtered, and then the solvent was removed under reduced pressure, to yield a white solid, 213 mg (85%). Mp = 192–194°C; 1H-NMR (300 MHz, CDCl3): δ ppm 0.94 (t, J = 7.5 Hz, 3H, -CH2CH3); 1.40–1.52 (m, 2H, -OCH2CH2CH2CH3); 1.71–1.80 (m, 2H, -OCH2CH2CH2CH3); 4.11 (t, J = 6.6 Hz, 2H, -OCH2); 7.05–7.10 (m, 1H, Ar-H); 7.28 (dd, J = 9.0, 2.4 Hz, 1H, Ar-H); 7.41 (d, J = 2.4 Hz, 1H, Ar-H); 7.48–7.58 (m, 2H, Ar-H); 7.69 (dd, J = 8.7, 2.1 Hz, 2H, Ar-H); 7.85–7.94 (m, 2H, Ar-H); 8.05 (d, J = 9.0 Hz, 1H, Ar-H); 8.49 (d, J = 1.8 Hz, 1H, Ar-H); 11.18 (br s, 1H, -SO2NH-); 13.95 (br s, 1H, -COOH); EI-MS: m/z 399 (C21H21NO5S, M+); CHN found C: 63.45, H: 5.50, N: 3.51; calc. for C21H21NO5S C: 63.14, H: 5.30, N: 3.51.

Purity of compounds 2–12.

For compounds 2, 3, 5, 7, 8, 11, and 12, HPLC purity was determined using an Agilent Eclipse C18 column (4.6×50 mm, 5 µm) with a flow rate of 1.0 mL/min, detection at 254 nm, and an eluent system of: A = H2O with 0.1% TFA; B = MeOH. The following gradient was applied: 0–3 min, 30% B; 3–18 min, 30% B→80% B; 18–23 min, 80% B; 23–30 min, 80% B→30% B; run time = 30 min; T = 25°C.

3-(Quinoline-8-sulfonamido)benzamide (2): Retention time: 5.59 min, HPLC purity: 99.06%.

N-(4-Hydroxyphenyl)quinoline-8-sulfonamide (3): Retention time: 11.20 min, HPLC purity: 96.12%.

4-(4-Ethoxyphenylsulfonamido)benzoic acid (5): Retention time: 13.86 min, HPLC purity: 99.56%.

5-Hydroxy-2-(4-propoxybenzamido)benzoic acid (7): Retention time: 19.65 min, HPLC purity: 100.0%.

2-(4-Propoxybenzamido)benzoic acid (8): Retention time: 22.56 min, HPLC purity: 98.62%.

5-Hydroxy-2-(3-propoxybenzamido)benzoic acid (11): Retention time: 19.96 min, HPLC purity: 99.38%.

2-(3-Propoxybenzamido)benzoic acid (12): Retention time: 22.92 min, HPLC purity: 99.41%.

Purity for compounds 4, 6, 9 and 10 was determined with elemental analysis.

4-(N-(4-Ethoxyphenyl)sulfamoyl)benzoic acid (4): CHN found C: 55.94, H: 4.79, N: 4.50; calc. for C15H15NO5S C: 56.06, H: 4.70, N: 4.36.

5-Bromo-2-(4-propoxybenzamido)benzoic acid (6): CHN found C: 54.01, H: 4.13, N: 3.77; calc. for C17H16BrNO4 C: 53.99, H: 4.26, N: 3.70.

5-Bromo-2-(3-propoxybenzamido)benzoic acid (9): CHN found C: 53.66, H: 4.22, N: 4.03; calc. for C17H16BrNO4 C: 53.99, H: 4.26, N: 3.70.

5-Methyl-2-(3-propoxybenzamido)benzoic acid (10): CHN found C: 68.99, H: 5.96, N: 4.51; calc. for C18H19NO4 C: 68.99, H: 6.11, N: 4.47.


Enzymatic inhibition assays for low affinity PBP2a and PBP5fm.

PBP2a from Staphylococcus aureus ATCC 43300 and PBP5fm from Enterococcus faecium D63r were overproduced and purified as described previously[13], [18].

Each of the purified PBPs (2.5 µM) were first incubated with 1 mM potential inhibitor in 100 mM phosphate buffer, 0.01% Triton X-100[19], pH 7, for 4 h at 30°C. Then, 25 µM fluorescein-labeled ampicillin[20] was added to detect the residual penicillin binding activity (RA). The samples were further incubated for 30 min at 37°C in a total volume of 20 µL. Denaturation buffer was added (0.1 M Tris/HCl, pH 6.8, containing 25% glycerol, 2% SDS, 20% β-mercaptoethanol and 0.02% bromophenol blue) and the samples were heated to 100°C for 1 min. The samples were then loaded onto a 10% SDS-acrilamide gel (10×7 cm) and electrophoresis was performed for 45 min at 180 V (12 mA). Detection and quantification of the RAs were with Molecular Image FX equipment and Quantity One software (BioRad, Hercules, CA, USA). Three independent experiments were carried out for each inhibitor.

Enzymatic inhibition assays for PBP2x 5204.

PBP2x-5204 from Streptococcus pneumonia[12] and N-benzoyl-D-alanyl-thioglycolate S2d[21], [22] were prepared as previously described. All assays with PBP2x 5204 were carried out in 96-well microtiter plates (Brand, Wertheim, Germany). PBP2x 5204 (0.6 µM) was incubated in the presence of the potential inhibitors in 10 mM sodium phosphate buffer (pH 7.0) containing 70 mM D-alanine and 0.01 mg/mL BSA, for 4 h at 25°C. This preincubation was used to also detect slow binding inhibitors. After the preincubation, the RA of PBP2x 5204 was determined. The initial rate of hydrolysis of 1 mM S2d in the presence of 1 mM DTNB was determined by monitoring the increase in absorbance at 412 nm (DTNB: ε[Δ ε] = 13600 M−1 s−1) using a microplate absorbance reader (Power Wave X, Biotek Instruments, Winooski, U.S.A.). The rate of spontaneous hydrolysis of S2d in the presence of the potential inhibitors was also determined in the absence of PBP2x 5204. All of the assays were carried out in triplicate. The determination of the RA of PBP2x 5204 in the absence of inhibitors was carried out six times on each plate. A test compound was considered as an inhibitor if the RA was <80%. In this case, to reveal false positives, the assays were also carried out under the same conditions in the presence of 0.01% Triton X-100. As described in the literature, promiscuous inhibitors (false positives) are slow binding, noncompetitive inhibitors. To avoid detailed kinetic investigations[8], it is possible to identify such compounds by carrying out the assays in the presence of Triton X-100[14], [19]. Promiscuous inhibitors show no inhibition in the presence of Triton X-100. The IC50 values in the presence of Triton X-100 were determined if the RAs were <50%. (RA: ∼50%, IC50∼c, c: concentration of compound in the assay; RA >50%, IC50 > c). The RA was measured over a range of concentrations, from which the IC50 values were determined by non-linear regression analysis, using Sigma Plot (Systat software) and fitting the data to the equation y = y0+(a×b)/(b+x)[23].

Antibacterial activity.

Determination of the antibacterial activities was carried out on microtiter plates, in 200 µL (final volume) of Müeller-Hinton Broth (MHB), following EUCAST (European Committee on Antimicrobial Susceptibility testing)/CLSI (Clinical and Laboratory Standard Institute) recommended procedures[24], [25]. The compounds were solubilized in MHB, just before use. Inocula were prepared for each strain by resuspending isolated colonies from 18 h cultured plates. Equivalents of 0.5 Mac Farland turbidity standards (approximately 1×108 CFU mL−1) were prepared in saline solution (0.085% NaCl) and then diluted 200-fold in MBH. MICs were determined as the lowest dilution of product that showed no visual turbidity.


The authors would like to thank André Zapun and Thierry Vernet, IBS, Grenoble, France, for providing purified PBP2x 5204, and Eric Sauvage and Chris Berrie for critical reading of manuscript.

Author Contributions

Conceived and designed the experiments: ST OV AA AZ AL BJ SG. Performed the experiments: ST OV TG MŽ JH IS AA AZ. Analyzed the data: ST OV AA AZ AL BJ SG. Contributed reagents/materials/analysis tools: AA AZ AL BJ. Wrote the paper: ST IS AA AZ AL BJ SG.


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