Antibiotic binding releases autoinhibition of the TipA multidrug-resistance transcriptional regulator

Investigations of bacterial resistance strategies can aid in the development of new antimicrobial drugs as a countermeasure to the increasing worldwide prevalence of bacterial antibiotic resistance. One such strategy involves the TipA class of transcription factors, which constitute minimal autoregulated multidrug resistance (MDR) systems against diverse antibiotics. However, we have insufficient information regarding how antibiotic binding induces transcriptional activation to design molecules that could interfere with this process. To learn more, we determined the crystal structure of SkgA fromCaulobacter crescentus as a representative TipA protein. We identified an unexpected spatial orientation and location of the antibiotic-binding TipAS effector domain in the apo state. We observed that the a6–a7 region of the TipAS domain, which is canonically responsible for forming the lid of antibiotic-binding cleft to tightly enclose the bound antibiotic, is involved in the dimeric interface and stabilized via interaction with the DNA-binding domain in the apo state. Further structural and biochemical analyses demonstrated that the unliganded TipAS domain sterically hinders promoter DNA binding but undergoes a remarkable conformational shift upon antibiotic binding to release this autoinhibition via a switch of its a6–a7 region. Hence, the promoters for MDR genes including tipA and RNA polymerases become available for transcription, enabling efficient antibiotic resistance. These insights into themolecular mechanism of activation of TipA proteins advance our understanding of TipA proteins, as well as bacterial MDR systems, andmay provide important clues to block bacterial resistance.

Investigations of bacterial resistance strategies can aid in the development of new antimicrobial drugs as a countermeasure to the increasing worldwide prevalence of bacterial antibiotic resistance. One such strategy involves the TipA class of transcription factors, which constitute minimal autoregulated multidrug resistance (MDR) systems against diverse antibiotics. However, we have insufficient information regarding how antibiotic binding induces transcriptional activation to design molecules that could interfere with this process. To learn more, we determined the crystal structure of SkgA from Caulobacter crescentus as a representative TipA protein. We identified an unexpected spatial orientation and location of the antibiotic-binding TipAS effector domain in the apo state. We observed that the a6-a7 region of the TipAS domain, which is canonically responsible for forming the lid of antibiotic-binding cleft to tightly enclose the bound antibiotic, is involved in the dimeric interface and stabilized via interaction with the DNA-binding domain in the apo state. Further structural and biochemical analyses demonstrated that the unliganded TipAS domain sterically hinders promoter DNA binding but undergoes a remarkable conformational shift upon antibiotic binding to release this autoinhibition via a switch of its a6-a7 region. Hence, the promoters for MDR genes including tipA and RNA polymerases become available for transcription, enabling efficient antibiotic resistance. These insights into the molecular mechanism of activation of TipA proteins advance our understanding of TipA proteins, as well as bacterial MDR systems, and may provide important clues to block bacterial resistance.
From bacteria to humans, cells employ multidrug resistance (MDR) systems to respond to and scavenge a wide variety of structurally and chemically diverse cytotoxic compounds (1,2). In addition to the well-known efflux pump-mediated MDR mechanisms, cytoplasmic-soluble proteins are also able to recognize and sequester many toxic compounds or drugs (3,4). The expression of both MDR transporters and cytoplasmic responders is often regulated by drug-sensing transcription factors that directly recognize and interact with the corresponding substrates (5,6). By the combined chemoprotective actions of MDR proteins and soluble drug sensors, cytotoxic compounds are promptly detected and effectively removed from the interiors of cells (5,7). Multidrug (MD) recognition by MDR and regulatory sensor proteins is often achieved in an adaptable and versatile MD-binding pocket with multiple binding capabilities for diverse ligands, and global conformational transformations induced by ligand-pocket binding promote active transport or transcription activation (8)(9)(10)(11).
The TipA (thiostrepton-induced protein A) class of transcriptional regulators found in diverse bacteria is viewed as a minimal autoregulated MDR system (12)(13)(14). TipA proteins belong to a subset of the superfamily of mercuric ion resistance (MerR)-like transcriptional regulators (15,16) that contain an N-terminal helix-turn-helix (HTH) motif followed by an intermediate linking coiled-coil (PF00376 MerR and PF13411 MerR_1 families in the Pfam database) and a C-terminal TipAS-type effector domain (PF07739 TipAS family in the Pfam database) (Fig. 1A). Investigation of Streptomyces lividans had revealed that expression of the tipA gene with two alternative start codons produces two protein isoforms: a fulllength transcriptional regulatory TipAL protein and a short TipAS protein consisting only of the C-terminal domain of TipAL (17)(18)(19). The TipAS protein is the predominant form that is capable of recognizing thiopeptide compounds via covalent binding by an active cysteine (13,20), which then induces structural reordering to form a large hydrophobic cleft for permanent sequestration and neutralization of the antibiotics (14,18). However, upon thiopeptide binding into the C-terminal TipAS domain, the N terminus of TipAL (TipAN) is activated to bind promotors via the HTH domain and promote transcriptional activation of multiple genes, including tipA for antibiotic resistance (14,21).
In addition to S. lividans, TipA-class proteins have also been reported to have crucial regulatory functions in other species such as Mta (multidrug transporter activation protein) from Bacillus subtilis (22), stationary-phase regulation of KatG protein (SkgA) from Caulobacter crescentus (23), and AlbA (albicidin resistance protein) containing two tandem TipAS domains from Klebsiella oxytoca (21,24). Structural analyses using apo and mta promoter-bound structures of the Mta N terminus (MtaN) revealed that MtaN possesses a canonical MerR-type HTH motif that binds promoter DNA to activate transcription using a distortion mechanism identical to BmrR, which belongs to another MerR-type MDR gene regulator family with a GyrI-like effector domain (25,26).
However, because of the lack of ligand-bound full-length structural information, whether TipA-class regulators also adopt a drug-induced activation mechanism similar to BmrR, which was elaborated by the analysis of the liganded BmrR-bmr promoter complex structure, remains unknown (27)(28)(29).
Previous NMR studies with accurate determinations of apo and liganded TipAS proteins indicated that thiopeptide binding induces stabilization and restructuring of the flexible N-terminal region and thus results in the formation of a large MD-binding pocket (14,18). Nevertheless, it is still a missing part in the current model of how this kind of drug-induced change in the TipAS domain drives a global structural shift to facilitate transcriptional activation of TipAN in the context of full-length TipAL protein (Fig. 1A).
Here, we sought to obtain full-length structural information of TipA-class proteins, and the SkgA structure was successfully determined at a resolution of 2.5 Å. The solved structure indicated a significantly different orientation of the TipAS effector domain compared with the GyrI-like effector domain of BmrR. Structural and biochemical analyses indicated that the interaction of TipA regulators with promoter DNA is hindered in the apo state and revealed an unexpected activation mechanism in which drug binding induces conformational turnover of The structure of TipA proteins is constituted mostly by a-helices with initial four helices within the DNA-binding domain, an intermediate coiled-coil a5 helix responsible for the dimerization, and the rest of the eight helices composing the TipAS domain. B, crystal structure of SkgA with one molecule in the asymmetric unit. The 2F o 2 F c density map is contoured at 1s. The a6-a7 region is highlighted in the right panel with ribbon representation for main chain and stick representation for side chain. N-ter, N terminus; C-ter, C terminus. C, dimeric structure of SkgA that is constructed by molecules from two adjacent asymmetric units. The protein surface is shown in the lower panel with buried area colored in blue. AM, asymmetric molecule. D, the a6-a7 region is involved in the dimeric interface. The a6-a7 region of one protomer interacted with the N-terminal DNA-binding domain of the other protomer. Amino acid residues of the a6-a7 region involved in the interaction are labeled with side chains shown as sticks. E, interactions between the a6-a7 region and N-terminal DNA-binding domain. Hydrogen bonds and salt bridges formed between residues are indicated by black and yellow dotted lines, respectively. The other labeled residues are involved in hydrophobic interactions. F, schematic diagram showing the interactions between the a6-a7 region and a1-a2 region in the SkgA dimer. G, schematic diagram showing the interactions between the a6-a7 region and a3-a4 region in the SkgA dimer.
the TipAS domain to release the N-terminal HTH motif for promoter DNA binding and subsequent transcriptional activation, during which the a6-a7 region may serve as a key switch element to drive the global transition. Remarkably, further biochemical results strongly support the above conclusion by showing that mutations on the drug-recognizing sites within the a6-a7 region resulted in no significant loss of drug-binding affinity but a sharp reduction of promoter DNA-binding affinity. Overall, our findings provide a crucial complement to the current understanding of TipA-class MDR systems.

Results
Basic architecture and dimeric interaction of C. crescentus TipA-class protein SkgA Full-length proteins of three reported TipA-class transcriptional regulators, S. lividans TipAL, C. crescentus SkgA, and B. subtilis Mta were expressed, purified, and set up for crystallization. As a result, diffraction-quality crystals of SkgA were obtained, and the structure was determined at a resolution of 2.5 Å using the single-wavelength anomalous dispersion phasing method (Table 1). SDS-PAGE analysis indicated that the crystals were composed of full-length SkgA proteins (Fig. S1A). Although full-length SkgA (residues 1-255) protein was used for crystallization, only residues 1-138 were observed in the final structure. The established structure consists of the N-terminal MerR-type HTH motif, coiled-coil region, and the initial two a-helices of the C-terminal TipAS domain ( Fig. 1B and  Because MerR family proteins reportedly function as dimers and SkgA protein also exhibits a dimer conformation in solution (Fig. S2A), a dimeric SkgA structure was established by combining two molecules from two adjacent asymmetric units for subsequent analysis ( Fig. 1C and Fig. S2B). The a6-a7 region of the SkgA dimer does not show any significant crystal contact with other symmetry mates (Fig. S2C). The dimeric interface was analyzed by the programs PyMOL and PISA (30). The total surface area of the SkgA dimer is 15,051.4 Å 2 , and the buried area is 5,404.7 Å 2 ( Fig. 1C and Fig. S2B). Remarkably, apart from the coiled-coil a5 helices, the a6-a7 region and Nterminal domain are also involved in the dimeric interface. Fifteen residues of the a6-a7 region of each protomer interact with the N-terminal domain of the other protomer via hydrogen bonding, ionic bonding, and hydrophobic interactions ( Fig.  1, D-G), which contribute to stabilization of the conformation of the a6-a7 region. Eleven residues of the N-terminal a1-a2 region exhibit interactions with ten residues of the a6-a7 region via hydrophobic interactions and three hydrogen bonds formed by residue pairs Tyr 4 -Asp 117 , Ser 16 -Glu 133 , and Tyr 23 -His 132 (Fig. 1, E and F). Twelve residues from the N-terminal a3-a4 region interact with eleven residues of the a6-a7 region via hydrophobic interactions, a salt bridge of Arg 44 -Asp 117 , and four hydrogen bonds of Arg 44 -Met 115 , Gln 51 -Leu 120 , Arg 57 -Lys 128 , and Arg 57 -Gln 129 (Fig. 1, E and G).
Similar results were found in the structure of Listeria monocytogenes TipA-class protein Lmo0526 with modeled a6-a7 helices (PDB code 3QAO) (Fig. S3A). The a6-a7 region of , where I hl is the lth observation of reflection h, and ,I h . is the weighted average intensity for all observations l of reflection h.
where F obs(h) and F cal(h) are the observed and calculated structure factors for reflection h, respectively. d R free factor was calculated same as R work factor using the 5% the reflections selected randomly and omitted from refinement.
Lmo0526 also exhibits a wide interaction with the N-terminal DNA-binding domain in the Lmo0526 dimer via hydrogen bonding, ionic bonding, and hydrophobic interactions (Fig. S3, B-E), which is in line with the corresponding interaction in the SkgA dimer. The a6-a7 region of the Lmo0526 dimer also does not exhibit any significant crystal contact with other symmetrical molecules (Fig. S3F). Notably, many of these interacting residues are conserved among the TipA-class family proteins, and the corresponding residues of some antibiotic-binding residues reported in TipA and DNA-binding residues revealed by MtaN-DNA and TipAN-DNA structures are involved in the interaction (Fig. S4). Collectively, these findings suggested that the a6-a7 region of the TipA-class proteins, which is reportedly unstructured flexible loops in unliganded TipAS protein (14,18), is stabilized with an ordered conformation via interaction with the N-terminal domain in the apo state.

The effector domain exhibits a distinctive orientation in TipA proteins
To confirm whether the in-solution conformation of the a6-a7 region is consistent with the conformation in crystal structures, double-cysteine mutants of TipA-class proteins were constructed and analyzed. In light of the structures, the conserved interacting residue pairs Ser 16 -Glu 133 of SkgA and Ser 13 -Glu 131 of Lmo0526 exhibit close distances ( Fig. 2A and Fig. S4). Therefore, double-cysteine mutants, SkgACC (S16C/ E133C), MtaCC (S15C/E138C), and TipALCC (T15C/E134C), were constructed based on sequence homology (Fig. S4) and were analyzed by both reduced and nonreduced SDS-PAGE. As a result, although WT SkgA, Mta, and TipAL were shown as monomer bands, the double-cysteine mutants were all shown as dimer bands in the nonreduced SDS-PAGE gel as a result of the formation of disulfide bonds ( Fig. 2A, right panel). The results indicated that in solution, the a6-a7 region of the TipA-class protein exhibits a conformation consistent with that revealed by SkgA and Lmo0526 structures.
Alignment of the two structures indicated that the a6 helices share a high structural similarity, whereas the a7 helices differ slightly in length and direction. However, notably, in the two structures, the a6-a7 helices can be seen to consistently extend from the a5 helix toward the DNA-binding interface, indicating that the relative orientation of the TipAS domain in TipA proteins is significantly different from the relative orientation of the GyrI-like effector domain in BmrR (Fig. 2B).
The a6-a7 region and TipAS domain hinder promoter DNA binding in the apo state Because multiple DNA-binding residues are involved in the dimeric contacts with the a6-a7 helices (Fig. S4) that exhibit an unexpected orientation, we further sought to investigate how the a6-a7 region and TipAS domain with the orientation affect DNA binding. SkgA and Lmo0526 structures were aligned on Ca atoms with the B-DNA-bound TipAN structure (PDB code 2VZ4) and distorted DNA-bound MtaN structure (PDB code 1R8D), respectively. Notably, it is currently unclear whether SkgA binding to DNA will result in DNA distortion, as observed in published MerR-DNA complexes, or remain B-DNA in form, as seen in the TipAN-DNA complex. Putative shifts of the a2 and wing region required for DNA binding were indicated by the structural superposition ( Fig. 2C and Fig.  S5) as previously elaborated by structural studies on MtaN (25,26). Importantly, the a7 helix, which is situated closely to the a2 helix, was found to occupy a part of the space for the putative bound DNA, which suggested that it may hinder both DNA loading and the movement of the a2 and wing regions for DNA binding and thus inhibit DNA association ( Fig. 2C and Fig. S5). Analysis of the electrostatic distribution of the a6-a7 region was also performed using the two structures, as well as the NMR structure of TipAS (PDB code 2MC0). As a result, with a relatively high sequence homology (Fig. 2D), the a6-a7 surfaces of all three structures are strikingly electronegative, (Fig. 2E), which would likely impair DNA binding.
Fluorescence polarization assays (FPAs) were performed to test the structure-based hypothesis that a6-a7 plays a key role in communication between the ligand-binding and DNA-binding regions. TipAL, TipAN, and a truncated protein consisting of TipAN and the a6-a7 region (TipAH7, TipAL residues 1-140) were purified for the first assessment, and all of them were found to be dimers in solution (Fig. 3A). The affinities with the tipA promoter DNA (ptipA) were measured as 44.0 6 5.1, 380.2 6 56.0, and 318.5 6 58.5 nM for TipAN, TipAL, and TipAH7, respectively (Fig. 3B), indicating ptipA-associating affinities of TipAL and TipAH7 significantly lower than the ptipA-associating affinity of TipAN. The double-cysteine mutant TipALCC was also applied for the analysis and showed a complete loss of DNA-binding ability (Fig. 3B). Parallel experiments were also performed for Mta and SkgA proteins, and consistent results were obtained. Full-length proteins and truncated proteins containing the a6-a7 region, MtaH7 (Mta residues 1-144), and SkgAH7 (SkgA residues 1-141), all exhibited a drastic loss of promoter DNA-binding affinity compared with the respective N-terminal constructs, and the double-cysteine mutants (MtaCC and SkgACC) did not show any specific binding with their respective promoter DNA (Fig. 3, C and D).
Based on the sequence homology shared by TipA-class proteins (14), including the a6-a7 region ( Fig. 2D and Fig. S4), a possible structural model of unliganded full-length TipA proteins was established via an alignment at a structured part of the a7 helix of TipAS and Lmo0526 (residues 133-139 of TipA and residues 130-136 of Lmo0526) (Fig. 3E).
Drug-binding induces a structural shift of the a7 helix for DNA binding Because the above structural and biochemical analyses indicated that the TipAS domain inhibited TipAN-DNA binding by directly hindering access of DNA to the HTH motif in the apo state, we further investigated how drug binding induces activation. Eight residues within the a6-a7 region are reportedly involved in the TipA-thiopeptide interaction (14), half of which (Phe 123 , Tyr 131 , Val 135 , and Trp 139 ) are highly conserved in the TipA family, and their corresponding residues in unliganded SkgA and Lmo0526 participate in the dimeric interaction described above. Importantly, Phe 123 , Phe 126 , Tyr 131 , Val 135 , and Trp 139 were shown in van der Waals contact with thiopeptides, the latter three of which make key contributions to the thiopeptide recognition of TipA on the a7 helix (14) (Fig.  4, A and B). Therefore, we sought to first investigate changes in the a7 helix upon ligand binding.
The homologous a6 helices exhibit a relatively ordered and conservative structure in SkgA, Lmo0526, and ligand-bound TipAS structures, so the three structures were aligned at a6 helices for comparison (residues 111-121 of Lmo0526, residues 114-124 of SkgA, and residues 113-123 of TipAL). As a result, the a7 helix and a6-a7 linking loop of thiopeptide-bound TipAS exhibit distinctive positions and directions relative to the a6 helix compared with those of SkgA and Lmo0526 structures (Fig. 4C), which suggests that a structural shift of the a7 helix occurs upon drug binding to release DNA-binding domains. Further, by a close-up view of the interacting residues, Phe 123 and Phe 126 of ligand-bound TipAS were observed to show significant positional discrepancies with their corresponding residues in SkgA and Lmo0526, indicating that thiopeptides may induce a shift of the a7 helix via a redirection of the loop region induced by interactions with Phe 123 and Phe 126 (Fig. 4D).

Drug-induced activation of TipA-class regulators
Mutagenesis and biochemical analyses were further performed to test the structural hypothesis that a shift of the a7 helix would be promoted by interactions of thiopeptides with Phe 123 and Phe 126 . F123A and F123A/F126A mutants of TipAL were produced, and their thiopeptide-binding affinities were assessed by isothermal titration calorimetry (ITC) as 7.12 6 0.95 and 13.20 6 1.36 mM, respectively. The affinity for WT TipAL was 5.23 6 0.84 mM (Fig. 4E). F123A and F123A/F126A mutants both showed only a slight decrease in thiopeptide affinity, ;1.4and 2.5-fold lower than the thiopeptide affinity of the WT, which agrees with the results of a previous report indicating that the two sites do not make a key contribution to the drug recognition of TipA (14). Next, ptipA-associating affinities of WT TipAL and the two mutants in the presence of thiostrepton were measured by FPA as 30.2 6 3.7, 227.6 6 25.9, and 317.1 6 51.4 nM, respectively (Fig. 4F). By thiostrepton binding, TipAL gained an ;12.6fold increase in ptipA affinity, whereas the ptipA binding of F123A or F123A/F126A did not show such a significant rise in the presence of thiostrepton (Figs. 3B and Fig. 4F). Collectively, these biochemical results indicated that although mutations in Phe 123 and Phe 126 caused no significant decrease in thiopeptide-binding affinity, they highly disrupted thiopeptide-induced activation of TipA-ptipA binding. Their double-cysteine mutants were also included in the assessment. The data were plotted using a base 10 logarithmic scale for the x axis and were fitted with a one-site binding model using the program GraphPad Prism7. E, the potential location of apo-state TipAS domain revealed by structural alignment. Structures of Lmo0526 and TipAS (PDB code 2MC0) were aligned at conserved and ordered a7 helices of relatively high sequence homology (indicated by a red arrow), and TipAN structure was further aligned to Lmo0526 (left panel). By the alignment, a possible ligand-free model for full-length TipA-class proteins was established with the TipAS domain lying beneath the HTH DNA-binding domain, which represents an inactive autoinhibited conformation (right panel).

A structural switch of the a6 helix is involved in transcriptional activation
In terms of the overall structure, such a structural shift of the a7 helix with a fixed a6 helix will lead to excessively close contact between TipAS and TipAN domains, which is still not reasonable for TipAN-ptipA interaction. Because the Ile 112 residue in the loop N-terminal to the a6 helix reportedly also interacts with the thiopeptide and its corresponding residue in apo SkgA is involved in the dimeric interface (Figs. 2D and 4A), we further sought to analyze whether the a6 he-lix also undergoes structural changes upon drug binding. The structure of Lmo0526, which exhibits a higher sequence similarity with TipAS than SkgA on the loop region and a7 helix, was used for structural comparisons with the TipAS-thiopeptide structure.
First, the two structures were aligned at the a6 helix (residues 111-121 of Lmo0526 and residues 1132123 of TipAL) to probe potential changes of surrounding loop regions upon thiopeptide binding. The results indicated that the Phe 123 -thiopeptide interaction probably leads to extension and stabilization of Drug-induced activation of TipA-class regulators the a6 helix, which is also shown in Fig. 4, and more importantly, the loop N-terminal to the a6 helix may undergo a significant deflection via the Ile 112 -thiopeptide interaction (Fig. 5A). Next, the structures were aligned at the ordered part of the a7 helix with relatively high identity (residues 130-136 of Lmo0526 and residues 133-139 of TipA) to evaluate variations of in the a6 helix. A significant discrepancy was observed in the orientations of a6 helices between the two structures, suggesting a drug-induced structural deflection of the a6 helix.
A two-site TipAL mutant, I112A/F123A, was then constructed to verify the structural hypothesis that the a6 helix would undergo a deflection upon drug binding. Its thiopeptide-binding affinity was measured by ITC as 7.51 6 0.87 mM (Fig. 5C), without a significant difference from the thiopeptide-binding affinity of WT and F123A. However, FPA results indicated that I112A/F123A in the presence of thiostrepton showed a further lower ptipA affinity of 685.3 6 97.9 nM (Fig. 5D), ;23-fold smaller than the ptipA affinity of the WT TipAL. Taken together, the above structural and biochemical results consistently suggested that thiopeptide binding promotes a structural switch of the a6 helix for transcriptional activation.

Discussion
Because the worldwide emergence of bacterial antibiotic resistance poses a major threat to public health, investigations on different bacterial resistance strategies are of great urgency for the development of new antimicrobial drugs (31). TipA-class transcriptional regulators compose a large family with ;2,500 members from 1,934 species currently in the Pfam database (Fig. 1A). This family constitutes a sensitive autoregulated MDR system in that the MDR functional elements as drug sensor, transcriptional activators, and drug neutralizers are all integrated within a single tipA gene and executed by its two translation products (14). Although the molecular mechanisms of DNA binding of its MerR-like domain and antibiotic recognition of the TipAS domain have been independently well-elaborated (14,18,20,24,26), how drug binding promotes its transcriptional activation remains largely unclear (Fig. 1A).
The a6-a9 region involved in antibiotic recognition was revealed to be flexible loops in apo-state TipAS (14,18), but it may result from a lack of the N-terminal part, especially a coiled-coil a5 helix that contributes to both dimerization and stabilization. Both the reported SkgA structure and the homologous Lmo0526 structure showed a structured conformation of a6-a7 helices ( Fig. 1 and Figs. S2 and S3), indicating the structural difference of this region between full-length and Cterminal isoforms. Interestingly, our findings revealed that in addition to the coiled-coil region, the a6-a7 region is also involved in the dimeric interface and is stabilized via the interaction with the N-terminal DNA-binding domain in the unliganded state ( Fig. 1 and Fig. S3). The interacting residues include some putative drug-binding and DNA-binding residues (Fig. S4), suggesting inhibited DNA-binding and drug-binding abilities of unliganded TipA-class regulators. The conformation of the a6-a7 region was confirmed by analysis of doublecysteine mutants of SkgA, Mta, and TipAL ( Fig. 2A). Remarkably, a6-a7 helices exhibit an unexpected orientation that may lead to a distinctive ligand-free position of the TipAS domain compared with effector domains of other bacterial MDR regulators such as BmrR (Figs. 2B and 3E), which suggests that TipA proteins adopt a different drug-induced activation mechanism.
TipAN and MtaN are reportedly constitutively transcriptionally active in the absence of the TipAS domain (19,26), and consistent results were indicated by our FPA assays (Fig. 3, B and C), suggesting an autoinhibition-disinhibition mechanism for transcriptional activation of the TipA-class proteins. Based on our structural and biochemical analyses, the a7 helix exhibits negative charges situated within the intermediate cleft between two MerR-type HTH domains (Fig. 2, C and E, and  Fig. S5). Our FPA results showed that the a6-a7 helices largely inhibited the promoter DNA interaction of the HTH motifs in that a6-a7 containing truncations (TipAH7, MtaH7, and SkgAH7) exhibited ;4-7-fold lower DNA-binding affinity than those of N-terminal truncations (TipAN, MtaN, and SkgAN) (Fig. 3, B-D). Moreover, structural prediction via the alignment of a7 helices revealed that the rest of the TipAS domain occupies the putative space for bound DNA and therefore sterically hinders the entry of promoter DNA into HTH domains in the apo state (Fig. 3E). The structural hypothesis is supported by the FPA results that full-length TipAL, Mta, and SkgA exhibited even lower affinities, and specific DNA interactions were completely abolished for their double-cysteine mutants whose a6-a7 region was fixed by disulfide bonds ( Figs. 2A and 3A-D).
With such an apo-state assembly of DNA-and drug-binding domains, TipA proteins require a relatively large conformational change to release DNA-binding domains for transcriptional activation. Several residues within the a6-a7 region were reportedly employed in thiopeptide recognition of TipAS (Fig. 4, A and B), inducing restructuring, stabilization, and formation of a lid to finally sequester thiopeptides (14). In the context of full-length TipA proteins, although a6-a7 helices remain an ordered conformation without high flexibility, as shown in the structure of the TipAS protein, the surrounding loops still exhibit long and flexible conformations (Fig. 2B), which contribute to the conformational switch of the TipAS domain upon drug binding. By structural analysis, we found that three key residues in the surrounding loop region that are stabilized by the interaction with the DNA-binding domain ( Fig. 1 and Figs. S3 and S4), Ile 112 , Phe 123 , and Phe 126 , may undergo a large structural shift upon antibiotic binding to drive an overall switch of the TipAS domain. Drug-induced variations of Phe 123 and Phe 126 may coordinately lead to both a sharp switch, as well as stabilization of the a7 helix (Fig. 4, C and D), and those of Ile 112 and Phe 123 could cooperatively result in redirection and stabilization of the a6 helix (Fig. 5, A and B). Mutations on these sites showed no significant influence on the thiopeptide-binding affinity of TipAL but resulted in a great reduction (;7-26-fold) of its ptipA-associating affinity in the presence of thiostrepton (Fig. 4, E and F, and 5, C and D), which indicated their crucial roles in conformational switching for transcriptional activation rather than drug binding.
Based on our findings, a model was established to explain the activation mechanism of TipA-class regulators. Although promoter-DNA interaction is inhibited by the TipAS domain in the transcriptionally inactive apo state (Fig. 6, A and B, left panels), drug binding induces stabilization, restructuring, and a significant shift of the switch element (the a6-a7 region), which drives overall structural turnover of the TipAS domain to facilitate promoter DNA binding and subsequent recruitment of RNA polymerases (RNAPs) (Fig. 6, A and B, right panels).
Because TipAS confers a multiantibiotic binding capability and its residues involved in the drug-binding pocket show some sequence discrepancy among species, TipA-class regulators may respond to a different spectrum of antibiotics among evolutionarily remote bacteria. However, to date, although the autoregulated thiopeptide-resistance mechanism of TipA has been well-elucidated in S. lividans, the physiological functions and corresponding drugs of TipA-class proteins in other species remain mostly unreported and worth further investigation and identification. In addition, because the full-length structure model of TipA-class proteins is difficult to achieve by X-ray crystallography, CryoEM analysis on the TipA-DNA-RNAP complex is awaited for a better understanding of the activation dynamics.
In summary, our findings in this study demonstrated an unexpected autoinhibition/inhibition-release mechanism for transcriptional activation of TipA-class regulators. The a6-a7 region was revealed to serve as an activating switch that is responsible for driving a conformational transition for the release of transcriptional inhibition upon antibiotic binding. The findings provide a crucial improvement for the current model of the working mechanism of TipA-class regulators and contribute to a better understanding of the bacterial MDR system.

Experimental procedures
Cloning, expression, and purification The encoding genes of full-length and truncated S. lividans TipA (accession no. AAB27737.1), C. crescentus SkgA (accession no. AAF01797.1), and B. subtilis Mta (accession no. CAA69863.1) were PCR-amplified and cloned into a pET-28a vector containing a His 6 tag. All site-directed mutations were generated using the MutanBEST site-directed mutagenesis kit (Takara Bio, Dalian, China). The recombinant plasmids were sequenced and transformed into Escherichia coli BL21 (DE3) strains (Novagen, Darmstadt, Germany). A selenomethionine (SeMet) derivative of SkgA (SeMet-SkgA) was produced using the methionine biosynthesis inhibition method. Cells from a Drug-induced activation of TipA-class regulators single transformed clone were incubated in LB medium at 37°C until the A 600 reached 0.6-0.8 and then induced using 0.5 mM isopropyl b-D-thiogalactopyranoside at 16°C for 18 h. The cells were collected by centrifugation and lysed by sonication. The lysed cells were centrifuged at 35,000 rpm for 30 min, and the supernatants were used for purification.
Prior to biochemical use, the recombinant proteins were first loaded on a nickel-nitrilotriacetic acid column (Qiagen) with buffer consisting of 20 mM Tris-HCl, pH 7.5, 500 mM NaCl, and 5% (v/v) glycerol and eluted with 500 mM imidazole. The proteins were further purified using a HiLoad 16/60 Superdex 200 SEC column (GE Healthcare) with a buffer consisting of 20 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 5% (v/v) glycerol. For crystallization, an additional purification step using a Resource-Q column (GE Healthcare) was performed. The purified proteins were concentrated using ultrafiltration to 20 mg/ml, then quick-frozen in liquid nitrogen, and stored at 280°C.

Crystallization, data collection, and structure determination
Crystallization was conducted using the previously described hanging-drop vapor-diffusion method (32). Diffraction quality crystals of native SkgA and SeMet-SkgA were obtained with a reservoir solution containing 13% (v/v) ethanol, 100 mM NaCl, 5% 2-Methyl-2,4-pentanediol, and 100 mM Tris-HCl, pH 7.8. The obtained crystals captured using cryoloops were soaked in cryoprotectant solution (20% (v/v) glycerol in reservoir solution) for 1 s and were immediately flash-frozen and preserved in liquid nitrogen for the diffraction experiments. Diffraction data were collected on Beamlines 17U1 and 19U1 at the Shanghai Synchrotron Radiation Facility at 100 K (33). The diffraction data sets were then processed using HKL-3000 (HKL Research Inc., Charlottesville, VA, USA).
The SeMet-SkgA structure was solved by the single-wavelength anomalous dispersion phasing technique using the AutoSol program as implemented in PHENIX (34). AutoSol found solutions, and the initial model was built automatically using AutoBuild in PHENIX and further refined using Refmac5 (35) and COOT (36). Then the model of SeMet-SkgA was utilized as the search model for molecular replacement determination of native SkgA structure using MOLREP (37). The model of SkgA was further refined at 2.50 Å resolution using Refmac5 and COOT. After several cycles of interactive refinements, we successfully established the model in the final structure. Both the coordinates and structure factors have been deposited in the PDB under accession code 7CLA. The statistical parameters for the data collection and refinement are summarized in Table 1.

SDS-PAGE
For analysis of SkgA crystals, crystals were captured using cryoloops, washed with reservoir buffer, and then processed for separation on a 15% SDS-polyacrylamide gel followed by Coomassie Brilliant Blue staining. For analysis of double-cysteine mutants of SkgA, Mta, and TipAL (SkgACC, MtaCC, and TipALCC), WT and mutant proteins were processed with normal sample buffer and nonreduced sample buffer without redox reagent, respectively, and applied for analysis on 15% SDS-polyacrylamide gel followed by Coomassie Brilliant Blue staining.

Size-exclusion chromatography assay
Analytical SEC assays were performed with a Superdex 200 10/300 column (GE Healthcare) on an AKTApurifier FPLC system (GE Healthcare). Purified full-length and truncated TipA proteins (40 mM) were loaded onto a column containing SEC buffer (20 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1 mM DTT) for assessment. The data analysis was performed using GraphPad Prism7 (GraphPad Software, San Diego, CA, USA).

Isothermal titration calorimetry
The ITC binding studies of the nosiheptide (Sigma) with WT TipAL and its mutants were performed using an ITC200 (GE Healthcare) at 298 K using a previously described protocol (38), with 60 ml of nosiheptide solution in the injector cell and 260 ml of protein solution in the sample cell. The injection volumes were set to 20 ml for all experiments, and two consecutive injections were separated by 2 min to reset the baseline. The control experiments, in which nosiheptide was titrated against the buffer, were also conducted, and the results were subtracted from the results of each standard experiment for adjustments. Three replicates were performed for each reaction. The final data were processed with a one-site fitting model using Microcal-Origin (OriginLab Corp, Northampton, MA, USA).

Fluorescence polarization assay
FPAs were performed in buffer consisting of 20 mM Tris-HCl, pH 7.5, 200 mM NaCl and 5% (v/v) glycerol at 298 K using a SpectraMax M5 microplate reader system (Molecular Devices, San Jose, CA, USA). The wavelengths of fluorescence excitation and emission were 486 and 525 nm, respectively. 26-bp dsDNA from the 210 and 235 regions of the tipA, mta, and skgA promoters with the sequences TTG-CACCTCACGTCACGTGAGGAGGC, TTGACCCTAACG-TTGCGTGATTGTTT, and TTGACCCTCACGCCACGT-CAGACCTG were synthesized with a 59-carboxyfluorescein label for the respective assays with TipAL, Mta, and SkgA proteins. For assays with thiostrepton supplementation, proteins were incubated with thiostrepton (Sigma) at a 1:1 ratio for 15 min prior to mixing with DNA in wells. Each well of a 384-well plate contained 10 nM of a fluorescently labeled DNA probe and different amounts of proteins with a final volume of 80 ml. DNA-free controls were included, and three replicates were performed for each reaction for each assay. The fluorescence polarization DP (in mP units) was calculated and fitted according to a one-site specific binding model using GraphPad Prism7 (GraphPad Software) with the function DP 5 DP max [protein]/(K d 1 [protein]).

Data availability
Atomic coordinates and structure factors for the reported crystal structure of C. crescentus SkgA have been deposited in the Protein Data Bank under accession number 7CLA.