This part of the methodology was based on the work by Chowdhury et al. to reproduce the full structure of LasR protein ¹ . The amino acid sequence of the LasR protein of P. aeruginosa was obtained from UniprotKB ²² (Uniprot ID: P25084). The crystal structure of the LasR protein LBD (amino acid residues 7 to 169) from P. aeruginosa was acquired from the Protein Data Bank ²³ (PDB ID: 3IX3). However, the entire structure of the LasR protein was required in order to have a better understanding of its molecular properties.

For this reason, the amino acid sequence (Uniprot ID: P25084) was used to search the PDB databank using BLASTp ²⁴ in order to identify suitable templates for homology modelling. The crystal structure of QscR bound to 3OC12-HSL was found to be the best fit based on sequence identity, query coverage, and E-value from the BLAST results (PDB ID: 3SZT) ²⁰ . The full list of similar structures obtained from the BLAST search are shown in Table 1.

As the current available crystal structures of LasR only contain the ligand binding domain ¹⁸ , we needed to reconstruct the full structure of LasR with the missing DNA-binding domain (DBD). The HHPred web server ²⁵ was used for homology modelling of the missing LasR DBD as was performed by Chowdhury et al. ¹ . The four templates used for homology modelling of the LasR DBD have the PDB identifiers 3SZT, 3IX3, 1FSE and 3ULQ. The experimental structure of LasR ¹⁸ and these templates were used to reconstruct the final model of LasR that contains both the LBD and the DBD. The final reconstructed model of the LasR protein was verified using PROCHECK ²⁵ (Figures S1 and S2, Extended data ²⁶ ), Verify3D ²⁶ and Ramachandran plots. More than 96.65% of the amino acid residues in the final reconstructed model had a 3D–2D score > 0.2 as indicated by Verify3D (Figure S3, see Extended data ²⁶ ). This score indicates a suitable computational model ²⁷ . The Ramachandran plot (Figure S1, see Extended data ²⁶ ) revealed that no amino acid residues were located in the disallowed regions. The ProSA ²⁸ value of this model was -6.69 which suggests that the quality of the homology model is high ²⁸ . Although the obtained model is slightly different from that obtained by Chowdhury et al. ¹ it is still viable.

The analysis of docking conformations and trajectories was performed using custom Python scripts (see Extended data ²⁶ ). These scripts use pandas v0.8.1 ²⁹ , scikit-learn v0.18.2 ³⁰ and MDTraj v1.9 ³¹ libraries. pandas ²⁹ facilitates data manipulation and analysis. In particular, it offers data structures and operations for manipulating numerical tables and time series. scikit-learn ³⁰ is a machine-learning library, which provides a set of common algorithms to Python users through a consistent interface. The MDTraj Python library ³¹ facilitates the combination of machine learning libraries such as scikit-learn for trajectory analysis. MDTraj serves as a bridge, connecting molecular dynamics (MD) data with statistics and graphics libraries developed for general data science users.

Diagrams of the interaction of 3OC12-HSL with LasR were obtained using LigPlot+ v.1.4 ³² using default parameters, which automatically generates 2D diagrams of ligand–protein interactions from 3D coordinates by loading the coordinate files in pdb format. Plot visualization was carried out using matplotlib v2.0.1 ^{32, 33} with seaborn v0.8.1 ³⁴ . The seaborn library aims to make visualization a central part of exploring and understanding data. It also provides a concise, high-level interface for drawing statistical graphics. Figures and videos were prepared with PyMOL v1.9.0.0 ³⁵ , VMD 1.9.3 ³⁶ and UCSF Chimera v1.11.2 ³⁷ . VMD ³⁶ is often used for this purpose as it has the ability to read trajectory files created during simulations in formats produced by many different software packages. PyMOL ³⁵ and UCSF Chimera ³⁷ are also commonly used by researchers and produce high quality images but are typically less straightforward to use for viewing and making videos of the trajectories.

The analysis protocol was similar to the work of Wolf et al. ³⁸ and Zamora et al. ³⁹ , using PCA and cluster analysis modules within scikit-learn v0.18.2. Principal component analysis (PCA) is an unsupervised statistical technique that is often used to make data easy to explore and visualize. PCA tries to explain the maximum amount of variance with the fewest number of principal components ⁴⁰ . The process of applying PCA to a protein trajectory is called essential dynamics (ED) ^{41, 42} . PCA analysis, performed using Cartesian coordinates, has become an important tool for the examination of conformational changes. Default parameters within the scikit-learn library were used. Cluster analysis is another unsupervised technique that tries to identify structures within data. It is a data exploration tool for dividing a multivariate dataset into groups. Clustering algorithms can be grouped into partitional and hierarchical clustering approaches ⁴³ . kmeans algorithm ^{44, 45} was used for molecular docking analysis. Agglomerative clustering using Ward’s linkage ⁴⁶ was used for molecule dynamics trajectory analysis with the connectivity matrix built on the basis of the k-Neighbors graph ³⁰ . Default parameters within the scikit-learn library were used.

Molecular dynamics (MD) simulations of all systems were conducted with the GROMACS suite, version 5.1.2 ⁴⁷ , utilizing the Amber ff99SB-ILDN force field ⁴⁸ , which exhibits considerably better agreement with NMR data than other forcefields. In all cases, short-range non-bonded interactions were cut off at 1.4 nm. The Particle mesh Ewald (PME) method ^{49, 50} was used for the calculation of long-range electrostatics.

LasR monomer simulation. In order to generate the starting structure of the LasR monomer before docking, the Las R molecule was placed in a dodecahedron box of TIP3P water ⁵¹ . After that, 100 mM NaCl was added, including neutralizing counterions. Following two minimizations by the method of steepest descent algorithm, the LasR monomer was equilibrated in two stages. The first stage involved simulating for 200 picoseconds under a constant volume (NVT) ensemble. The second stage involved simulating for 200 picoseconds under a constant pressure (NpT), maintaining pressure isotropically at 1.0 bar. Production simulation was conducted for 100 nanoseconds in the absence of any restraints. The temperature was sustained at 300 K using the v-rescale ⁵² algorithm. For isotropic regulation of the pressure, the Parrinello-Rahman barostat ⁵³ was used. This combination of thermostat and barostat use ensures that an adequate NpT ensemble is sampled. Finally, the trajectory of the LasR monomer simulation was used for the calculation of chemical shifts. SPARTA+ v2.90 ⁵⁴ and SHIFTX2 v1.10 ⁵⁵ were used to predict the chemical shifts of the protein backbone atoms with the help of the MDTraj wrapper functions ³¹ . Both programs have been proven to be remarkably accurate, especially for predicting ¹³C shifts ⁵⁴ . This was used to validate whether the force field is appropriate for further investigation. The final extracted structure that was used for docking and MD simulations was also verified with Gaia ⁵⁶ from the Chiron webserver ⁵⁷ , which compares the intrinsic structural properties of in silico protein models to high resolution crystal structures.

Molecular dynamics simulations using docking poses. The 3D model of 3OC12-HSL was obtained from PubChem (CID: 127864) ( Figure 2) ⁵⁸ . It has been shown that docking has its limitations ⁵⁹ . For this reason, after finishing the molecular docking simulations of 3OC12-HSL with LasR, the docking poses were extracted to perform molecular dynamics (MD) simulations. The ligand parameters for the molecular dynamics simulations were calculated for the General Amber Force Field (GAFF) ⁶⁰ using the ACPYPE tool ⁶¹ with AM1-BCC partial charges ⁶² and generation of a GAFF topology. A time step of 2 femtoseconds was used during heating and the production run and coordinates were recorded every 1 picosecond. Three simulations of 300 nanoseconds were performed. Further details about the simulation protocol can be found in ‘LasR monomer simulation’ section.

To build the LasR–ligand complex, the ligand 3OC12-HSL was docked with the LasR monomer using AutoDock Vina v1.1.2 ⁶³ . However, AutoDock Vina currently uses several simplifications that affect the obtained results. The most notable simplification, as the creators note ⁶³ , is the use of a rigid receptor. The amount of computation used during a docking experiment is determined by a parameter called ‘exhaustiveness’ in AutoDock Vina ^{63, 64} . However, the default exhaustiveness value is 8 and the creators claim that increasing this value leads to an exponential increase in the probability of finding the energy minima ^{63, 64} . The conformational space of the whole protein was searched using grid box dimensions 60×62×48Å. The following exhaustiveness values were tested in this study: 8, 16, 32, 64, 128, 256, 512, 1024, 2048 and 4096. The ligand and target structures containing hydrogen atoms were prepared using the AutoDockTools ⁶⁵ from MGLTools v1.5.6.

Principal component analysis (PCA) ⁴⁰ and cluster analysis using k-means clustering ^{44, 45} was performed (Figures S4 and S5, Extended data ²⁶ ). The results demonstrated that the number of interaction sites does not change for exhaustiveness values from 1024 to 4096. An exhaustiveness value of 1024 was chosen as it provides good results, good speed and thorough sampling of the docked configurations. The exhaustiveness value was set to 1024 and the maximum number of binding modes to generate was set to 20. After that, 100 independent docking calculations were carried out with random initial seeds. The target was taken from the molecular dynamics simulation of the LasR monomer. Water molecules were removed from the structure.

We also performed another set of docking simulations using AutoDock Vina v1.1.2 ⁶³ , rDock v2013.1 ⁶⁶ and FlexAID v2.48 ⁶⁷ . We performed 10 docking simulations using each program. Each individual run was set to generate 20 docked poses. For AutoDock Vina, we performed one docking run for each exhaustiveness value: 8, 16, 32, 64, 128, 256, 512, 1024, 2048 and 4096.

Docking was also performed using the rDock program ⁶⁶ which was previously found to be successful in predicting the binding mode for the CCDC-Astex set of 85 diverse protein–ligand complexes in approximately 80% of cases ⁶⁶ . A cavity with a radius of 36 Å was set and centred on the LasR monomer to cover the whole protein surface and define the docking volume. AutoDock Vina and rDock were chosen based on the performance of these academic programs ⁶⁸ .

FlexAID (parameters are available in Extended data ²⁶ ) was also used as, unlike other programs, it is robust against increasing structural variability ⁶⁷ . FlexAID performs better than AutoDock Vina in all scenarios against non-native complex structures ⁶³ . FlexAID uses a soft and smooth scoring function based on contact surfaces which is different from Autodock Vina and rDock. FlexAID was run using default parameters.

g_mmpbsa v1.6 ⁶⁹ was used for the evaluation of binding energies. It was also used for the estimation of the energy contribution of each residue to the binding energy. g_mmpbsa calculates the relative binding energy rather than the absolute binding energy, so the entropy contribution (T∆S) is not evaluated ⁶⁹ . From the two simulations with length of 300 nanoseconds, we cut out 10 nanoseconds with an interval of every 120 picoseconds for the calculation of binding energies. g_mmpbsa uses the MM-PBSA approach, which has grown to be one of the most widely used methods to compute interaction energies and is often employed to study biomolecular complexes ⁶⁵ .

To find out whether 3OC12-HSLs interact with conserved amino acid residues, we performed multiple sequence alignment (MSA) using the R msa package v1.4.5 ⁷⁰ . ClustalW ⁷¹ , Clustal Omega ⁷² and MUSCLE ⁷³ within the msa package were used to carry out multiple sequence alignments. ClustalW and MUSCLE are commonly and widely used, while Clustal Omega is a more recent and powerful method that is used when aligning a large number of sequences ⁷² . We performed multiple sequence alignment of the LasR protein and closest homologue sequences, based on the work by Chowdhury et al. ¹ . The consensus threshold parameter in msa was set to 75, the rest was set to default. Table 2 shows the sequences used for sequence alignment.

When docking homology models, it is preferable to have experimental evidence suggesting the general interaction site (within ~10 Å). Representative structures from molecular dynamics simulations were used for protein-protein docking using ClusPro v2.0 ⁷⁴ . ClusPro was chosen because it gave equivalent results to the best human predictor group according to the latest CAPRI experiments carried out in 2013 ⁶⁸ .

From the experimental X-ray data, it was found that ‘Trp152’, ‘Lys155’ and ‘Asp156’ play an important role during dimerization. The distance between ‘Trp152’ from chain A and ‘Asp156’ from chain B of the crystallographic structure was 0.276 nm and the distance between ‘Asp156’ from chain A and ‘Lys155’ from chain B was 0.279nm. These residues were used as attraction constraints.

We performed a simulation run of 100 nanoseconds using a standard MD protocol for the assessment of conformational changes of the LasR monomer. The overall stability of the molecule was assessed using the root-mean-square-deviation (RMSD) of the protein atoms. RMSD was calculated with reference to the initial frame through the time of the MD run (Figure S6, Extended data ²⁶ ). Another suitable measurement for the stability of the LasR monomer structure is the radius of gyration, which also shows the structure is stable (Figure S7, Extended data ²⁶ ).

During the examination of MD trajectories, principal component analysis (PCA) ⁴⁰ is usually used for the visualization of the motion of the system ( Figure 3a). Generally, in order to capture more than 70% of the variance in the trajectory data, the first handful of components are sufficient ³⁹ . PCA can uncover the fundamental movements contained in an MD trajectory, however, it does not group the snapshots into different clusters ⁴³ . This can be accomplished by clusterization of the PCA data.

Cluster analysis was performed on the LasR monomer simulation for the selection of an initial starting structure to study docking. Identifying a distinct, representative structure of the cluster allows blind docking to be performed on the whole structure. It should be also noted that cluster analysis allows the evaluation of the frequent conformations of LasR. For the clustering analysis, we chose agglomerative clustering using Ward’s linkage ⁴⁶ . This algorithm appears to be the most appropriate as it is deterministic, allowing for reproducibility of the resulting clusters, thus minimizing the amount of bias.

We performed several rounds of agglomerative clustering using Ward’s linkage. The accuracy of the clustering was assessed with the help of the Davies–Bouldin index (DBI) ⁷⁵ , Dunn index ⁷⁶ , silhouette score ⁷⁷ and Calinski-Harabasz pseudo-F statistic (pSF) ⁷⁸ metrics. An optimal number of clusters were chosen, simultaneously accounting for low DBI, high silhouette, high Dunn index and high pSF values.

The distribution of clusters over the simulation is visualized in Figure 3b and the four clusters are: cluster 4 (black) at the beginning of the simulation (after equilibration), cluster 2 (green) in the middle, cluster 1 (light green) and cluster 3 (dark blue) at the end. The clusterization defined by the first two principal components ( Figure 3b) provides a coherent picture and it is also supported by good DBI, Dunn index, silhouette score and pSF values (Figure S8, Extended data ²⁶ ). Figure 3c shows clearly that the simulation has converged.

For validation of the molecular dynamics simulation quality, theoretical NMR shifts were calculated using Sparta+ ⁵¹ and ShiftX2 ⁵² . For the NMR shifts calculation, snapshots from cluster 3 ( Figure 3b) were used because of their stability. We compared NMR values of C-alpha atoms from the experimental NMR of the LBD with theoretical NMR values of the LBD from our molecular dynamics simulations (BMRB: 6271) ¹⁸ . Unfortunately, the current available NMR information only includes the 173 amino acid residues of the LBD. In Figure 4, one can see that simulated NMR shift values from the two programs are close to the experimental data, thus demonstrating the quality of the MD simulation of the LasR monomer.

It should be noted this protein becomes partially soluble when the ligand interacts with it ¹⁸ . The differences between the theoretical chemical shifts and experimental values could be attributed to: 1) the theoretical model does not involve the interaction with the ligand 2) the experimental NMR only includes information about the LBD and not the DBD, which can affect the LBD.

After that, the representative structure ( Figure 5c) was extracted from cluster 3 ( Figure 3c) to study docking. The representative structure of the LasR system and its differences from the homology modelled structure ( Figure 5b) are visible in Figure 5c. Secondary structure analysis of the representative structure was performed using PDBSum ⁷⁹ (Figure S9, Extended data ²⁶ ). Finally, the extracted centroid structure was validated using Gaia ⁵⁶ (Figure S10, Extended data ²⁶ ), which also shows the model is of a high quality. Therefore, in this study, a model has been developed to include the dynamics of the full-length LasR molecule (residues 1 to 239) and it has been shown that the dynamics of the complete C-terminal region of LasR modulate the N-terminal region, as will be discussed later.

In this study, a molecular docking approach was used to inspect the possible binding modes of 3OC12-HSL with the LasR monomer. PCA and cluster analysis were performed on docking data ( Figure 6a, b) and the results show three binding sites. Cluster 2 corresponds to experimental data, while cluster 1 and cluster 3 do not ( Figure 6c). These results clearly support the findings of Bottomley et al. ¹⁸ , who also demonstrated that 3OC12-HSL binds to the LBD.

We performed several rounds of k-means clustering. The accuracy of the cluster analysis was evaluated using the DBI ⁷⁵ , Dunn index ⁷⁶ , silhouette score ⁷⁷ and pSF ⁷⁸ metrics (Figure S11, see Extended data ²⁶ ). An optimal number of clusters were chosen for docking analysis, simultaneously accounting for low DBI, high Dunn, high silhouette and high pSF values. We generated 2000 docked poses and performed representative structure extraction for use in MD simulations of the LasR 3OC12-HSL binding sites. The representative structures were produced by identifying the centroid conformations of the clusters using the following algorithm:

S i j = e – β d i j / d s c a l e (eq. 1 )

Where s _ij is the pairwise similarity, d _ij is the pairwise distance, and d _scale is the standard deviation of the values of d to make the computation scale invariant.

a r g m a x i ∑ j S i j (eq. 2 )

Representative structures from each cluster were extracted for further use in MD simulations. The binding energy of the representative structure of cluster 1 is -5.4 kcal/mol and the mean binding affinity for the whole cluster is -5.257 ±0.233 kcal/mol. Cluster 1 contains 839 docked poses from a total 2000 (41.95%). For cluster 2, the binding affinity of the representative structure is -5.1 kcal/mol and the mean for the whole cluster is -5.593 ±0.386 kcal/mol. These results correspond to the experimental binding site data ¹⁸ . Cluster 2 contains 864 docked poses from a total of 2000 (43.2%). For cluster 3, the representative structure features the highest binding affinity of -5.7 kcal/mol and the mean binding affinity for the whole cluster is -5.264 ±0.27 kcal/mol. Cluster 3 contains 297 docked poses from 2000 (14.85%) which does not correspond to the experimental binding site.

It has been suggested that molecular docking is not appropriate for the prediction of binding affinity or binding poses of protein-ligand complexes. However, docking analysis can still provide important information regarding potential binding sites and the resulting poses can be used for MD simulations ^{59, 80} .

We also ran another set of simulations to corroborate the blind docking with other molecular docking software, including AutoDock Vina ⁶³ , rDock ⁶⁶ and FlexAID ⁶⁷ ( Figure 7). All three programs, which each use different algorithms, suggest that there are two potential binding sites. One is within the LBD, which corresponds to experimental data ¹⁸ , and the other is within the ‘bridge’. PCA of the results from these docking programs was performed for easier comprehension (Figure S12, Extended data ²⁶ ).

In total, 900 nanoseconds of MD simulations have been performed and used for the analysis of 3OC12-HSL interaction with the LasR monomer. The representative structures were taken from docking results ( Figure 6c) and used as starting points for MD simulations with LasR. Simulations were conducted for a sufficient time to allow the positions of 3OC12-HSL to reach equilibrium in the LasR molecule.

The stability of the molecule was evaluated by calculating the RMSD of the backbone atoms. RMSD was calculated with reference to the initial snapshot. Figure 8a shows that Simulation 2 and 3 experience a substantial RMSD deviation from the initial starting point. Simulation 2 corresponds to cluster 2 in the docking simulations, while Simulation 3 corresponds to cluster 3 ( Figure 8a). For Simulation 1, which corresponds to cluster 1, the 3OC12-HSL molecule did not fixate and reach equilibrium and therefore no further analysis was performed ( Figure 8a) for this simulation. Simulation 2 shows that after 230 nanoseconds, the structure becomes stable. For Simulation 3, the structure changes its conformation at 100 nanoseconds and becomes stable between 260 nanoseconds and 300 nanoseconds. Simulation 2 and 3 represent the binding sites predicted by all docking programs from Figure 7. Calculation of the root-mean-square fluctuation (RMSF) was used to evaluate the flexibility of the LasR monomer. The average per-residue RMSF was calculated for each simulation run ( Figure 8b).

It is visible in Figure 8b that the residues from 165 to 176, which correspond to beta turns in the SLR of LasR, are highly mobile. Simulations 2 and 3 show that 3OC12-HSL has two binding modes, one with the LBD ( Figure 9a), which corresponds to experimental data and one with the LBD-SLR-DBD bridge of LasR ( Figure 9d).

PCA and cluster analysis were performed on simulation 2. Hydrogen bond analysis was also performed, based on cut-offs for distance and angles according to the Wernet-Nilson criteria ⁸¹ using MDTraj ³¹ . During the simulation, 3OC12-HSL forms hydrogen bonds with Tyr56, Ser129 and Trp60, which is in agreement with experimental data ¹⁸ (Figure S14, Extended data ²⁶ ). Over the course of simulation 2, 3OC12-HSL also establishes a large number of hydrophobic contacts with the amino acid side chains of the LasR LBD ( Figure 9b). This phenomenon is not unexpected, given the large hydrophobic surface area of the LasR LBD and the low solubility of 3OC12-HSL in water. 3OC12-HSL has hydrophobic interactions mainly with amino acids from helix 3, helix 5 and sheet 1 side chains. RMSD analysis of the conformations of LasR with and without 3OC12-HSL bound to the LBD gives a value of 7.027 Å between the conformations (Figure S16, Extended data ²⁶ ). RMSD of the modelled full structure of LasR with ligand superimposed onto the experimentally obtained tertiary structure of LBD of LasR with ligand gives a value of 1.692 Å, where RMSD <2 Å in relation to the experimentally studied structure ( Figure 9c). Residues that participate in hydrophobic interactions and hydrogen bonding are shown in Figure 9e and Figure S18 and 19 (Extended data ²⁶ ).

The second binding mode involves the interaction of 3OC12-HSL with the LBD-SLR-DBD bridge. PCA, cluster and hydrogen bond analysis were also performed on simulation 3. Over the course of simulation 3, 3OC12-HSL establishes hydrogen bonds and a large number of hydrophobic contacts with amino acid side chains in the beta turns of the LasR SLR. In simulation 3, 3OC12-HSL forms hydrogen bonds mainly with the ‘Lys182’ and ‘Leu177’ beta turn residues. RMSD analysis of the two conformations of the LasR monomer and when LasR is bound to 3OC12-HSL via the DBD gives a value of 1.677 Å (Figure S20, see Extended data ²⁶ ). Residues that participate in hydrogen bonding and hydrophobic interactions are shown in Figure S16. Complete data sets for MD simulations are available as extended data (Figures S13-S20 ²⁶ ).

In order to analyse the binding sites in detail, MM-PBSA ⁶⁹ binding energy calculations were performed for each binding site based on the MD trajectories. The binding energy calculations demonstrated that the interaction of the ligand with the LBD-SLR-DBD bridge is not competitive with its interaction with the LBD ( Table 3). Analysis of the energy terms demonstrated that only polar solvation energy contributes positively. However, for the interaction with the “the bridge”, the electrostatic interaction energy is 3.6 times higher than the energy for the LBD interaction.

This suggests that a combination of Van der Waals, electrostatic interaction and non-polar solvation energy contribute to the stability of the LasR-3OC12-HSL binding complex. To assess which amino acids are involved, we performed analysis of the energy contribution of residues to binding for both simulations obtained from MM-PBSA calculations using g_mmpbsa. Sequence alignment was performed using the R msa package ⁷⁰ . ClustalW ⁷¹ , Clustal Omega ⁷² and Muscle ⁷³ algorithms were used for sequence alignment. Full alignments using these algorithms are available as extended data ²⁶ . Analysis suggested that LasR residues Tyr64, Tyr56, Trp88, Leu36 and Trp60 contribute the most to binding with 3OC12-HSL ( Figure 10a), with a binding energy of approximately -128.578 kJ/mol ( Table 3).

Energy calculations to assess residue interactions and sequence alignment show that 3OC12-HSL interacts with highly conserved amino acid Trp60, which agrees with experimental data ⁸² . The interaction also involves nine other conserved amino acids; Tyr64, Asp73, Pro74, Val76, Phe102, Phe103, Ala105 and Gly113 ( Figure 10b). In total, 16 amino acids that contribute to the interaction have over 75% conservation.

Analysis suggested that ligand residues Leu236, Leu177, Val176, Phe219, Lys182 and Trp19 contribute the most ( Figure 10c) to the newly described binding state involving ‘the bridge’ of LasR, with a binding energy of approximately -166.456 kJ/mol ( Table 3). The analysis of residue sequence alignment shows that 3OC12-HSL interacts with highly conserved amino acids such as Leu236, Leu177, Phe219 and Trp19 ( Figure 10d). The 3OC12-HSL interacts with 12 fully conserved amino acids in this case. In total, 16 amino acids participate in the interaction, where amino acid conservation is more than 75%. In this new binding site, Trp19 and Asp156 of the LBD, Leu177 of the SLR and Arg180, Glu181, Glu196, Lys218, Arg224 and Lys236 of the DBD of LasR participate in the interactions with 3OC12-HSL. A lactone head group interacts with the conserved Trp19 of the LBD.

It is known that LasR binds to the corresponding promoter as a dimer ¹ after interacting with the autoinducer. Thus, monomeric LasR–3OC12-HSL complexes were subjected to dimerization as an additional experiment. The protein docking experiments using structures from MD runs were performed using ClusPro v2.0 ^{74, 83– 85} because of its success in the CAPRI (Critical Assessment of Predicted Interactions) scoring experiment. We used the centroid conformations of the LasR bridge-3OC12-HSL and LasR LBD-3OC12-HSL complexes from MD simulations. Then we performed protein docking using protein conformations without the ligands and used constraints based on the residue distances between monomers from the experimental data ¹⁸ . For the selection of the model, we used an approach recommended by the authors of ClusPro ⁷⁴ , which suggests finding the most populated clusters. For LasR bridge-3OC12-HSL complex docking, the top model contained 80 members and the scores by ClusPro for the docking model were -951.4 for the centre and -1332.0 and for the lowest energy region, suggesting a favourable binding mode ( Figure 11a). For the LBD LasR-3OC12-HSL complex, the top model contained 122 members and the scores for the docking model were -1440.7 for the centre and -1517.9 for the lowest energy region ( Figure 11b). Both docking structures feature negative energy and this could suggest the possibility of multiple docking conformations. It is possible that the multiple binding modes of 30C12-HSL imply that LasR has multiple dimerization interfaces like QscR ( Figure 11c) ²⁰ , which is a post-translational repressor of LasR. In the absence of 3OC12-HSL, it forms a heterodimer with LasR. It appears this protein may have a much more delicate regulation than was initially thought.

All data underlying the results are available as part of the article and no additional source data are required.

Zenodo: Interaction of N-3-oxododecanoyl homoserine lactone with transcriptional regulator LasR of Pseudomonas aeruginosa: Insights from molecular docking and dynamics simulations. https://doi.org/10.5281/zenodo.2586559 ²⁶

This project contains the following extended data:

Data are available under the terms of the Creative Commons Attribution 4.0 International license (CC-BY 4.0).