Binding and unbinding of transcription regulators at operator sites constitute a primary mechanism for gene regulation. While many cellular factors are known to regulate their binding, little is known on how cells can modulate their unbinding for regulation. Using nanometer-precision single-molecule tracking, we study the unbinding kinetics from DNA of two metal-sensing transcription regulators in living Escherichia coli cells. We find that they show unusual concentration-dependent unbinding kinetics from chromosomal recognition sites in both their apo and holo forms. Unexpectedly, their unbinding kinetics further varies with the extent of chromosome condensation, and more surprisingly, varies in opposite ways for their apo-repressor versus holo-activator forms. These findings suggest likely broadly relevant mechanisms for facile switching between transcription activation and deactivation in vivo and in coordinating transcription regulation of resistance genes with the cell cycle.
Binding and unbinding of transcription regulators at operator sites constitutes a primary mechanism for regulating gene expression, and they are often rate-determining for regulatory responses1,2,3. For binding to an operator site, its rate is readily modulated by many cellular factors such as regulators’ cellular concentration and the chromosome organization4,5,6,7,8,9,10,11. For unbinding from an operator site, it is unclear whether these factors can modulate its rate for regulation. At least, regulator unbinding from an operator site on DNA is presumed to be a unimolecular reaction and thus independent of regulators’ cellular concentration. Surprisingly, recent in vitro studies revealed that CueR, a Cu+-sensing efflux regulator, can undergo assisted dissociation and direct substitution processes on its cognate DNA; both lead to its concentration-dependent unbinding rate from a recognition site on DNA and may facilitate CueR in deactivating transcription12. This unusual concentration-dependent unbinding was also reported recently for nonspecific chromosomal organization proteins13, DNA polymerase14 and a single-strand-DNA-binding protein15, all functionally unrelated to CueR. Moreover, using force to apply tension, which changes DNA conformation, can modulate protein unbinding kinetics from DNA16,17.
Despite the above discoveries in vitro, it remains unknown whether concentration- and DNA-conformation-dependent protein unbinding from DNA is relevant in vivo. Here using stroboscopic single-molecule tracking (SMT)2 to image protein−DNA interactions in real time and at nanometer spatial resolution, we study the quantitative DNA interaction kinetics of CueR and its Zn2+-sensing homologue ZntR in living Escherichia coli (E. coli) cells. CueR and ZntR, both belonging to the MerR-family regulators, bind tightly to their respective dyad-symmetric recognition sequences within σ70-dependent suboptimal promoters, either repressing or, with Cu+ or Zn2+ bound (10−21 M affinity and 10−15 M affinity, respectively18,19), activating the transcription of efflux genes to defend against metal stress19,20,21. We find that in living E. coli cells, CueR and ZntR show striking concentration-dependent unbinding kinetics from chromosomal recognition sites in both their apo and holo forms. Unexpectedly, their unbinding kinetics further varies with the extent of chromosome condensation, and more surprisingly, varies in opposite ways for apo-repressor versus holo-activator forms. These findings suggest novel mechanisms for facilitating transcription deactivation and activation in vivo and in coordinating transcription regulation of resistance genes with the cell cycle, which are likely broadly relevant for gene regulation.
Concentration-dependent regulator residence time
To visualize CueR or ZntR in living cells, we made its functional fusion with the photoconvertible fluorescent protein mEos3.2 (refs 22, 23; that is, CueRmE or ZntRmE) at its chromosomal locus as well as in a plasmid for varying its cellular concentration (Methods and Supplementary Note 2). We used time-lapse stroboscopic imaging2,24,25,26,27,28,29 to track the positions over time of single photoconverted mEos3.2-tagged proteins in a cell at tens of nanometer precision until their mEos3.2 tags photobleached (Fig. 1a; Methods and Supplementary Note 5.2). For each tracked protein molecule, we obtained its time trajectory of displacement r per time-lapse (that is, the distance the protein molecule travelled between two consecutive images) (Fig. 1a,b). This SMT approach, along with single-cell total fluorescence counting, also enabled us to quantify the copy number of CueR or ZntR in each cell (Methods and Supplementary Note 5.3). By sorting the cells into groups of similar cellular protein concentrations, we could analyse protein-concentration-dependent processes without being limited by the large cell-to-cell heterogeneity in protein expression levels (Supplementary Note 5.3).
We first examined and , whose metal-binding cysteines were mutated to make them permanently locked in the apo-repressor forms (that is, C112S for CueR18 and C115S for ZntR30). The displacement-versus-time trajectory of a single (or ) in a cell shows clear transitions between large and small r values; the small r values are expected to be dominated by protein binding to chromosome, thus being nearly stationary (Fig. 1b). Thresholding the displacement-versus-time trajectory with an upper displacement limit r0 (for example, r0=220 nm; see later for justification of this value) selects out those small displacements and gives the estimates of the individual time durations (that is, the microscopic residence time τ) of a single protein molecule at a chromosomal binding site. Each microscopic residence time τ starts when r drops below r0 and ends when r jumps above r0 (for example, τ1 in Fig. 1b) or when the mEos3.2-tag photobleaches/blinks (for example, τ2 in Fig. 1b). By measuring many individual τ’s from a large number of single-molecule displacement trajectories, we obtained the average residence time 〈τ〉 for each cell, whose cellular concentration of (or ) was also determined (Fig. 1c).
Strikingly, the average residence time 〈τ〉 decreases with increasing cellular concentration of or (Fig. 1c,d). This trend is independent of the value of the thresholding r0 and persists after correcting for the contribution of mEos3.2 photobleaching/blinking kinetics (Supplementary Note 8). Free mEos3.2, which does not bind to DNA and exhibits much shorter apparent 〈τ〉, does not show this trend in the cell (Fig. 1d).
We next examined un-mutated CueRmE and ZntRmE in cells grown with 100 μM Cu2+ or Zn2+ in the medium (that is, and ). These metal concentrations cause maximal induction of the cueR or zntR regulons in the cell30,31, and the regulators are largely metallated. Their 〈τ〉’s show differences from those of and , indicating that we indeed observe the behaviour of holo-regulators (Fig. 1c,d). Importantly, their average residence times on chromosome still exhibit a decreasing trend with increasing cellular protein concentrations (Fig. 1c,d). Therefore, for both apo and holo forms of CueR or ZntR, higher cellular protein concentrations shorten their average residence times on chromosome, suggesting concentration-enhanced protein unbinding kinetics from DNA.
Concentration-enhanced regulator unbinding
To quantify the variable motions of individual CueR or ZntR molecules in a cell, we determined their cumulative distribution functions (CDFs) of displacement r (Fig. 2a)32. Regardless of the metallation state of CueR or ZntR, global analysis of CDFs across all cellular protein concentrations resolves minimally three diffusion states with effective diffusion constants of ∼3.7 μm2 s−1, 0.7 μm2 s−1 and 0.04 μm2 s−1 (referred to as DFD, DNB and DSB, respectively; Methods and Supplementary Note 11). No subcellular localization or protein aggregation was observed, and hence these two are not the reasons for the presence of the resolved three diffusion states (Supplementary Note 13). We assigned these three diffusion states as proteins that are: freely diffusing (FD) in the cytoplasm; nonspecifically bound (NB) to and moving on chromosome (the contributions from nonspecific interactions with the plasmids in the cell is <7% and thus negligible; Supplementary Note 20.5); and specifically bound (SB) to chromosomal recognition sites, whose slow motions reflect the chromosome dynamics (and measurement uncertainties). Both experimental evidences and simulations (details in Supplementary Notes 12 and 15) support these assignments: (1) CueR or ZntR can bind to DNA specifically and nonspecifically12,21,33,34. (2) The three effective D’s are consistent with reported values for proteins freely diffusing in the cytoplasm, nonspecifically bound or specifically bound to chromosome2,25,28,32,35, when the cell confinement effect24 and the time-lapse effect of imaging32 are both taken into account. Note that the magnitude of the effective diffusion constant DFD here is smaller than that measured for free diffusing protein in vitro36; this apparent difference results from the cell confinement effect (Supplementary Note 15.2 and Supplementary Figs 35 and 36). (3) Control experiments on tracking free mEos3.2 in cells with variable time lapses show similar effective diffusion constants as the FD state (Supplementary Fig. 23). (4) Simulations of molecular diffusion in confined cell geometries. (5) Short-time movement analysis for the SB state agrees with the literature reported chromosome diffusion constant (Supplementary Fig. 26).
Moreover, the resolved CDF also gives the fractional populations (that is, percentages) of the CueR (or ZntR) in the FD, NB and SB states among all CueR (or ZntR) protein molecules in the cell. With increasing cellular protein concentrations, the fractional populations of DFD and DNB increase, while that of DSB decreases (Fig. 2c); these trends are consistent with that at higher protein concentrations, each protein molecule will spend more time freely diffusing or nonspecifically bound to the chromosome than specifically bound at recognition sites, as more protein molecules compete for the limited number of recognition sites. Deleting the cueO promoter (ΔPcueO), one of the many CueR operator sites, expectedly did not cause much perturbation, including CueRmE’s fractional population at the SB state (Fig. 2d and Supplementary Note 18.3). In contrast, deleting the zntA promoter (ΔPzntA), the only known ZntR operator site in E. coli, did decrease, but surprisingly did not abolish, ZntRmE’s SB state (Fig. 2d and Supplementary Note 18.3). This observation motivated us to identify many additional possible ZntR recognition sites in the E. coli genome (Supplementary Note 22).
The resolved CDF of r concurrently gives the corresponding resolved probability density function (PDF) of r (Fig. 2b), in which the three resolved peaks correspond to the FD, NB and SB states. The resolution of these three states in this PDF of r immediately justifies the r0 value that thresholds the displacement-versus-time trajectories—For r smaller than r0≈220 nm, >99% of SB states of CueR (or ZntR) are included, and the thresholded residence times τ are thus dominated by contributions from proteins specifically bound at chromosomal recognition sites (and those nonspecifically bound to chromosome at higher cellular protein concentrations), with very little contribution from freely diffusing proteins in the cytoplasm. To quantitatively deconvolute all possible contributions to τ, we formulated a minimal mechanistic model comprising the FD, NB and SB states (Fig. 2e and Supplementary Note 14). This model enabled us to analyse the distribution of τ to obtain , the apparent unbinding rate constant from recognition sites (Fig. 2f), as well as the fractional populations of different states to obtain other kinetic constants for protein binding and unbinding at recognition sites and nonspecific DNA sites (Methods, Table 1, and Supplementary Tables 7 and 8).
Strikingly, , the apparent unbinding rate constant from recognition sites, increases linearly with increasing cellular concentrations of the free (or total) or (Fig. 2g), in contrast to unimolecular reaction kinetics of protein unbinding from DNA where the unbinding rate constant is independent of free protein concentration. Linear fitting of versus free protein concentration gives the slope kf and intercept k−1, the facilitated (second order) and spontaneous (first order) unbinding rate constants from recognition sites, respectively. For or , the slopes are even steeper (Fig. 2g). Therefore, both apo and holo forms of CueR and ZntR have concentration-dependent unbinding kinetics from chromosomal recognition sites, where the dependence likely results from the assisted dissociation or direct substitution mechanism that we discovered for CueR−DNA interactions in vitro12 (see Discussion and Supplementary Fig. 41b and Supplementary Note 18.2)15,37,38,39,40.
Different extents of chromosome condensation among cells
We next examined the spatial distribution in a cell of the residence sites associated with the residence times of CueR and ZntR, which are dominated by their binding to chromosomal recognition sites and nonspecific sites (Fig. 1a insets). This distribution can reflect the chromosome organization41 because: (1) The recognition sites of CueR and ZntR spread across the chromosome randomly (Supplementary Note 22.3), (2) their nonspecific binding sites are expected to scatter across the chromosome randomly as well (Supplementary Note 20.6) and (3) contributions from nonspecific binding to the plasmids in the cell are negligible (<7%; Supplementary Note 20.5).
In some cells, these residence sites localize to a small region (Fig. 3a), reflecting that in these cells the chromosomes are highly condensed. In contrast, in some other cells, the residence sites spread over the cell (Fig. 3b), reflecting that the cells’ chromosomes are less condensed. We further directly imaged the Hoechst-dye-stained chromosomes in the cells. Consistently, some cells have compact chromosomes (Fig. 3d), while others have their chromosomes spread over the entire cell volume (Fig. 3e), reflecting again the different extents of chromosome condensation among the individual cells.
To quantify the extent of chromosome condensation for each cell, we computed the average pairwise distance 〈dij〉 between the residence sites as a measure. We validated this measure by comparing with results from direct imaging of dye-stained chromosomes (Supplementary Note 20.2). The distributions of 〈dij〉 among cells are broad (Fig. 3g,h), reflecting that the extent of chromosome condensation differs significantly from cell to cell. For cells expressing , for example, two subpopulations can be resolved, corresponding to those with more or less condensed chromosomes (that is, smaller or larger 〈dij〉, respectively; Fig. 3g).
Chromosome-organization-dependent regulator unbinding
We sorted the cells into three groups based on their 〈dij〉 to examine how the unbinding of CueR and ZntR from recognition sites may relate to chromosome organization. Within each group, we determined the dependence of , the apparent unbinding rate constant from recognition sites, on the cellular protein concentration. Remarkably, for and , while their preserve the protein-concentration dependence in each group, their in cells with more condensed chromosome (that is, smaller 〈dij〉) are up to three times smaller than those in cells with less condensed chromosome (that is, larger 〈dij〉; Fig. 4a and Supplementary Fig. 50c). As a control, we treated the cells expressing and with the drug chloramphenicol, which is known to cause chromosome compaction42. Consistently, this chloramphenicol treatment leads to a decrease of across all accessible cellular protein concentrations (Supplementary Note 21.5).
More surprisingly, an opposite trend applies to the metallated holo-proteins with regard to the dependences of their unbinding kinetics on the extent of chromosome condensation. For and , their are larger in cells with more condensed chromosomes (that is, smaller 〈dij〉) at any cellular protein concentration (Fig. 4b and Supplementary Fig. 50f).
We further obtained kf and k−1, the second-order facilitated and first-order spontaneous unbinding rate constants from recognition sites, for cells with different extents of chromosome condensation (Fig. 4a,b). Correspondingly, kf and k−1 both show opposite dependences on 〈dij〉 between the apo and holo forms of CueR or ZntR; and they can change by up to nine times with 〈dij〉 ranging from ∼0.5 to 1.2 μm (Fig. 4d,e, and Supplementary Note 21.3). Altogether, these results suggest that chromosome organization modulates both the facilitated and spontaneous unbinding of CueR and ZntR from recognition sites, but in opposite directions depending on the regulators’ metallation state.
The concentration- and chromosome-organization-dependent unbinding of CueR and ZntR from their recognition sites open up new possibilities for regulating transcription of their associated metal resistance genes. The concentration-dependent unbinding of CueR and ZntR, together with their spontaneous unbinding from DNA, may facilitate the switching between the transcriptionally activated state (bound holo-protein) and the repressed state (bound apo-protein), which both require protein binding to the same operator site (Supplementary Note 18.2). Transcription deactivation by these regulators will likely involve the unbinding of a promoter-bound holo-activator from DNA followed by binding of an apo-repressor, rather than the dissociation of the tightly bound metal from the promoter-bound holo-protein18,19, which is expected to be slow. For , just the basal concentration range of ∼17–240 nM (Supplementary Fig. 17) can already change its unbinding rate from a recognition site from ∼4.7 to 7.9 s−1, a ∼70% increase. On the other hand, transcription activation will likely involve the unbinding of a promoter-bound apo-repressor followed by binding of a holo-activator, rather than the direct metallation of the promoter-bound apo-repressor, which faces competition for the metal by many other apo-repressors in the cell43,44. For , the basal concentration range of ∼14–185 nM can change its unbinding from a recognition site from ∼8.3 to 9.8 s−1.
Mechanistically, concentration-dependent unbinding of CueR or ZntR from chromosomal recognition sites likely results from their assisted dissociation or direct substitution process, which we discovered previously in studying CueR interactions with a specific DNA in vitro (Supplementary Note 18.2)12. In the assisted dissociation process, a protein from the surrounding solution (for example, the cytoplasm) helps carry away the incumbent protein bound at the recognition site (Fig. 5d); in the direct substitution process, the incoming protein directly replaces the incumbent one (Fig. 5e); both processes depend on the protein concentration in the surrounding. Both of these processes likely involve a ternary complex as a common intermediate, in which two protein molecules each partially bind to the recognition site (Fig. 5c), as we proposed previously37. This ternary complex is possible because of the homodimeric nature of CueR and ZntR: they can form bivalent contacts with DNA in which their two DNA-binding domains bind to the two halves of their dyad-symmetric recognition sequences (Fig. 5a). Under thermal fluctuation, one of the DNA-binding domains of a protein molecule could transiently detach, allowing another protein from solution to bind to the vacant half dyad sequence, leading to a ternary complex (Fig. 5c). This ternary complex could then proceed in two possible pathways: both proteins fall off, resulting in an assisted dissociation (Fig. 5d), or one of the two proteins falls off, where 50% of the chance would result in a direct substitution (Fig. 5e). Although no evidence exists for higher-order oligomeric CueR or ZntR complexes on regular DNA, our previous in vitro study has revealed a related ternary complex in CueR interactions with an engineered DNA Holliday junction37,45. Relatedly, ternary complexes involving multivalent contacts with DNA were also proposed to rationalize the concentration-dependent unbinding from DNA of nonspecific chromosomal organization proteins38,39 that are dimeric and of a single-strand-DNA-binding protein15 that has multiple DNA-binding domains.
Regarding the correlation between the unbinding kinetics of CueR (or ZntR) and chromosome organization, as well as the opposite trends between their apo-repressor versus holo-activator forms, we postulate that they may help the cell modulate transcription of metal resistance genes during the growth cycle. The unbinding of apo- and holo-CueR (or ZntR) from recognition sites is important for activation and deactivation of transcription, respectively. Under optimal growth conditions without metal stress, cells divide frequently. The dividing cells tend to have highly condensed chromosomes5,7, which we verified by examining the spatial distribution of residence sites of CueR (or ZntR) on chromosome and by direct chromosome staining (Fig. 3c,f,i). Their highly condensed chromosomes should lead to slower unbinding of apo-CueR and apo-ZntR (that is, repressors) and faster unbinding of holo-CueR and holo-ZntR (that is, activators); both lead to less (now unneeded) activation of metal resistance genes, beneficial for saving energy for cell division. On the other hand, under metal stress conditions, cells barely divide and their chromosomes are less condensed (Fig. 3h versus Fig. 3i). Here apo-CueR or apo-ZntR unbinds faster from promoters, leading to more facile transcription activation to defend against metal stress. Moreover, holo-CueR or holo-ZntR unbinds slower here, which would keep activating transcription longer. Supporting this postulate, we found that the apparent unbinding rate constants () of and in dividing cells are indeed significantly slower than those in nondividing cells across all cellular protein concentrations (Fig. 4c and Supplementary Fig. 52c).
Mechanistically, the chromosome-organization-dependent unbinding of CueR and ZntR from recognition sites likely stems from their ability to impose DNA structural distortions. The holo forms of these regulators bend and unwind DNA at the recognition sites, as shown by structural studies of related MerR-family regulators in complex with DNA46,47. These protein-imposed DNA distortions should lead to a susceptibility of the protein−DNA complexes to mechanical tensions in DNA (Fig. 5a), and thus to chromosome organization16,17 in which the extent of condensation can exert variable tensions along the chromosome48,49 (Supplementary Note 21.6). This susceptibility should then give rise to dependences on chromosome organization for both spontaneous unbinding (Fig. 5b) and facilitated unbinding (Fig. 5d,e) of CueR and ZntR from their recognition sites. Moreover, it is known that apo and holo forms of MerR-family regulators distort DNA structure differently47,50,51,52,53 (the detailed structural differences are not yet defined though). These differences could be the reason that apo- and holo-CueR or ZntR respond to chromosome organization in opposite trends.
Many DNA-interacting proteins form multivalent contacts with DNA or impose structural distortions on DNA54. For the former, these proteins should thus be capable of forming ternary complexes at recognition sites on chromosome, making assisted dissociation or direct substitution processes possible. For the latter, their normal complexes should be susceptible to DNA tension and thus to chromosome organization. Therefore, the concentration- and chromosome-organization-dependent unbinding from recognition sites discovered here could be broadly relevant for protein−DNA interactions and gene regulation in cells.
Materials and sample preparation
All strains were derived from the E. coli BW25113 strain (Supplementary Note 2). CueRmE or ZntRmE was generated by fusing to the C terminus of CueR or ZntR the monomeric, irreversibly photoconvertible fluorescent protein mEos3.2 (that is, mE)22,23. The corresponding genes were integrated at the chromosomal loci via λ-RED homologous recombination55. An L-arabinose-inducible plasmid pBAD24 containing CueRmE or ZntRmE was further introduced to allow for variable protein expression. On the basis of the CueR and ZntR structures18, their C-termini are distant from their DNA-binding domains, and thus the fusion tag is expected to not interfere with DNA binding. Cell growth assays of mEos3.2-tagged strains in comparison with the wild-type and knockout strains show that both fusion proteins are functional (Supplementary Note 3). The intactness of the fusion proteins were examined via standard SDS–PAGE or western blot; for the latter, the fusion proteins were further tagged at the C-termini with the FLAG epitope (Supplementary Note 3). CueRmE is essentially intact in cells (estimated to have <8% cleaved mEos3.2, comparable to our measurement errors). ZntRmE shows significant degradation in cells, consistent with prior literature33. This degradation results in a time-dependent cellular concentration of mEos3.2-tagged ZntR during our imaging experiments, and our results thus reflect an averaged protein unbinding kinetics over the corresponding protein concentration range. Nevertheless, this degradation does not affect ZntR’s apparent unbinding rate constant from recognition sites, but its kf, the facilitated unbinding rate constant from recognition sites, is likely underestimated and its k−1, the spontaneous unbinding rate constant from recognition sites, is likely overestimated (Supplementary Note 17).
or was generated by mutating one of its Cu- or Zn-binding cysteines to serine (that is, C112S for CueR18 and C115S for ZntR30) to make it permanently apo and constitutively functional as a repressor. The corresponding genes were cloned in a pBAD24 plasmid, which was introduced into the ΔcueR or ΔzntR knockout strain, respectively. The ΔPcueO or ΔPzntA promoter knockout was done via λ-RED recombination in the ΔcueR or ΔzntR strain, respectively, into which the pBAD24 plasmid containing CueRmE or ZntRmE was introduced.
E. coli cells expressing mEos3.2-tagged CueR or ZntR were imaged at room temperature on an agarose pad sandwiched between a coverslip and a slide in a sealed chamber (details in Supplementary Note 4). The cells were first grown in LB medium overnight at 37°C. The cultures were then diluted 1:100 in (metal depleted) M9 medium supplemented with amino acids and vitamins and grown at 37 °C until OD600 reached 0.3, at which point L-arabinose was added to induce expression for 5–30 min. The cells were then recovered by centrifugation, washed, re-suspended in M9 medium containing glucose, MEM amino acids and MEM vitamins, and incubated for 60 min before being placed on a 3% agarose gel. Note that for metal stress conditions, CuSO4 or ZnSO4 solution was also added into the cell solution to a final concentration of 100 μM at this stage. Gold particles (100 nm) were drop-casted on the coverslip as position marks for drift correction. The cells are viable under our imaging conditions, with a doubling time of ∼250 min, similar to cells not exposed to the imaging lasers (Supplementary Note 4.2).
Based on the bright-field transmission images, single cells with an aspect ratio of ∼2.5 and having no visible division septum were analysed; they are referred to as nondividing cells. Under our experimental conditions, these single cells were in either B or C phase of the cell cycle, containing one or a partially replicated chromosome. Dividing cells (that is, cells showing a clear division septum, for example, Fig. 3c,f) were also analysed and they were in the D phase of the cell cycle containing two copies of chromosome (Supplementary Note 4.4).
SMT and cell protein quantification
Individual cells were studied using SMT via time-lapse stroboscopic imaging and single-cell quantification of protein concentration (SCQPC). Time-lapse stroboscopic imaging2,24,25,26,27,28,29 was adapted to track the motions of single photoconverted mEos3.2-tagged proteins in a cell for high temporal (that is, 4 ms) and spatial (that is, ∼20 nm) resolution, using an Olympus IX71 microscope and inclined epi-illumination (Supplementary Note 5). Single mEos3.2 photoconversion was achieved by controlling the power density and illumination time of a 405-nm laser. Short 561-nm excitation laser pulses (pulse duration Tint=4 ms) were synchronized with camera exposures so that even a fast-moving protein with a typical diffusion constant of 3–11 μm2 s−1 in bacterial cytoplasm would not move beyond a diffraction-limited focus during Tint. This stroboscopic imaging yielded a diffraction-limited fluorescence spot for a protein in an image, where the protein’s centroid could be localized to tens of nanometer precision through two-dimensional Gaussian fitting. By capturing images in a time-lapse manner (lapse time Ttl=30 to 400 ms; all data presented in the main text are at Ttl=60 ms), we could track the motion of each protein until its mEos3.2 tag photobleached (for example, Fig. 1a) and obtain the corresponding time trajectory of displacement r between adjacent images (for example, Fig. 1b). Individual molecules were probed using the 561-nm laser pulses for 30 imaging frames after each photoconversion. This photoconversion-imaging-and-bleaching cycle was then repeated for 500 times followed by the SCQPC step to quantify the rest of proteins that were not tracked.
In SCQPC (Supplementary Note 5.3), the remaining number of mEos3.2-tagged protein molecules in each cell was determined in two steps: (1) Photoconverting all of them to the red form and imaging the total red fluorescence intensity of the cell. (2) Dividing the total fluorescence intensity by the average fluorescence intensity of a single mEos3.2 (which was derived from the earlier SMT for the same single cell). Note that in step (1), depending on the amount of remaining mEos3.2, the EM gain of the camera was adjusted accordingly to ensure the fluorescence signal was within the linear regime of camera response. The fluorescence signal was then corrected by the EM gain to obtain the total fluorescence intensity for quantification. An important feature here was to use the single mEos3.2 fluorescence intensity determined in the same cell to eliminate the need to correct for power density differences of the imaging laser across the illumination area. The photoconversion efficiency (0.42)56,57 of mEos3.2 and the protein oligomeric state (CueR and ZntR are stable homodimers) were also included in determining the total copy number of CueR or ZntR in each cell. The protein copy number was converted to protein concentration by using the cell volume determined from its transmission image: the cell boundary was fitted with the model of a cylinder with two hemispherical caps as reported58 (Supplementary Fig. 13a). The quantification of each cell’s CueR or ZntR concentration allowed us to sort the individual cells into groups of similar cellular protein concentrations.
The overall imaging time for SMT and SCQPC processes for each cell is ∼30 min. This imaging time is much shorter than the average cell doubling time (∼250 min) under our conditions and the cell morphology stays the same throughout the measurements.
Analysis of single-molecule diffusive motions
The effective diffusion constants and fractional population of different states were extracted by analysing the CDF of displacement. Experimentally, the CDF of displacement r per time-lapse was constructed using only the first displacement of each position trajectory to prevent long trajectories from biasing the sampling32. After constructing CDFs across a range of cellular protein concentrations, we globally fitted them with a three-diffusion-state CDF (C3(r), equation (1) and Supplementary Equation 11, and Fig. 2a), which is a linear combination of three terms:
The corresponding three-state PDF of r, P3(r) is:
The approach of using a linear combination of diffusion terms in the CDF (or the corresponding PDF, Fig. 2b) of r was also applied previously by others to analyse SMT results and resolve multiple diffusion states of a protein in E. coli or mammalian cells1,2,24,27,32,35,59,60,61. This linear combination approach assumes an approximation of a quasi-static system, that is, interconversion between the diffusion states is slower than the experimental time resolution (see justification of this approximation for CueR or ZntR in Supplementary Note 18.4).
In the global fit, the effective diffusion constants (that is, DFD, DNB and DSB) were expected to be concentration independent and thus were shared across the cellular protein concentrations, while their fractional populations (that is, AFD, ANB and ASB=1–AFD–ANB) were allowed to differ (Supplementary Note 11.2). This global fitting was critical for the reliability of determining the minimal number of diffusion states, and their fitted diffusion constants and fractional populations, as compared with fitting the CDFs individually. Exemplary fitted fractional populations versus cellular protein concentrations are shown in Fig. 2c. The extraction of the number of diffusion states and their effective diffusion constants was validated through multistate diffusion simulations within the confined cell geometry, followed by the quantitative analysis of the simulated results in parallel to analysis of the experimental results (Supplementary Note 15).
Determination of from chromosomal recognition sites
A three-state kinetic model (Fig. 2e) was used to analyse the distributions of the microscopic residence time τ, thresholded from the displacement-versus-time trajectory to extract the apparent unbinding rate constant of mEos3.2-tagged regulators from chromosomal recognition sites (Supplementary Note 14). The three states are the freely diffusing CueR or ZntR proteins in the cytoplasm, nonspecifically bound to DNA and specifically bound to chromosomal recognition sites. This kinetic model includes the reversible binding/unbinding of a regulator to chromosomal recognition sites and nonspecific sites, as well as the photobleaching/blinking of the mEos3.2 tag, but the direct interconversion between the SB and the NB states is assumed to be sufficiently slow to be kinetically negligible (justification and validation of this approximation in Supplementary Note 14.5).
With a given displacement threshold r0, the effective diffusion constants (D’s), the unbinding rate constant (k−2) from the NB state, the apparent unbinding rate constant () from the SB state and the photobleaching/blinking rate constant kbl, we derived the respective probability distribution functions ϕ(τ) of the thresholded residence time τ for the FD, NB and SB states (that is, ϕFD(τ), ϕNB(τ) and ϕSB(τ), respectively; Supplementary Note 14.1):
where , and are the rate constants that account for the unbinding of a mEos3.2-tagged regulator from chromosome and/or mEos3.2 photobleaching/blinking. , and . With the fractional populations of FD, NB and SB states (that is, AFD, ANB and ASB) extracted from the global CDF analysis, at any cellular protein concentration, the overall probability distribution function of τ, ϕ(τ)all, is:
Here we independently determined kbl by analysing the distribution of length of the tracking trajectories (Supplementary Note 10). The unbinding rate constant k−2 from nonspecific sites was extracted by fitting the residence time distribution with equation (7) at the highest cellular protein concentration (for example, 1,375 nM for ), where ASB is ≤5% and ASBϕSB(τ) in equation (6) can be neglected and k−2 became the only floating parameter:
For any other cellular protein concentration with ASB>5%, the residence time distribution was fitted with equation (6), with predetermined D’s, A’s, kbl and k−2, and the only floating parameter was (for example, Fig. 2f). As both CueR and ZntR have many recognition sites and nonspecific binding sites in the E. coli chromosome (Supplementary Note 22), all determined rate constants here represent the average properties over all the possible sites.
The dependence of on the cellular concentration of the freely diffusing proteins (that is, [P]FD) was then fitted with the linear function (for example, Fig. 2g):
where kf is a second-order rate constant for facilitated unbinding and k−1 is the first-order rate constant for spontaneous unbinding from the recognition sites. And, [P]FD=[P]cellAFD, where [P]cell is the total cellular concentration of CueR or ZntR.
The entire procedure of extracting the unbinding rate constants from residence time distributions was also validated by simulations of three-state diffusion processes in confined cell geometry with variable interconversion rates (Supplementary Note 15.3). The results were further corroborated by hidden Markov model analysis of single-particle tracking trajectories using the vbSPT (variational Bayes Single Particle Tracking) software62 (Supplementary Note 16).
Population analysis of different states in the cell
The same three-state kinetic model also allowed us to analyse the relative populations of FD, NB and SB states of CueR or ZntR across all cellular protein concentrations. This analysis uses a quasi-equilibrium approximation, which assumes that a CueR or ZntR molecule can sample these three states rapidly relative to its cellular lifetime and thus all binding and unbinding are at equilibrium (justification and validation in Supplementary Note 14.3). Under this approximation, relative concentrations of the proteins at these three states can be related to the kinetic parameters in the model as in equations (9, 10, 11) (Supplementary Note 14.3). Here [P]FD, [PD]NB and [PD]SB are the cellular concentrations of freely diffusing CueR or ZntR proteins, proteins nonspecifically bound to DNA and proteins specifically bound chromosomal recognition sites, respectively. And, [P]FD=[P]cellAFD, [PD]NB=[P]cellANB and [PD]SB=[P]cellASB.
Here k1 and k2 are the binding rate constants to the recognition sites and nonspecific sites, respectively. k3 and k−3 are the interconversion rate constants between the SB and NB states, which are approximated to be sufficiently small to be kinetically negligible as mentioned above (validations in Supplementary Note 14.5). [D]SB, [D0]SB, [D]NB and [D0]NB are the effective cellular concentrations of vacant chromosomal recognition sites, total chromosomal recognition sites, vacant nonspecific binding sites and total nonspecific binding sites, respectively. Using k−2, k−1 and kf from the residence time analysis described earlier, we can fit ASB/AFD versus [P]FD, ANB/AFD versus [P]FD, ASB/ANB versus [PD]NB with equations (9, 10, 11) as in Supplementary Fig. 30 to obtain the dissociation constants of SB (KD1) and NB (KD2) states together with k2, [D0]NB, k1 and [D0]SB (Table 1 and Supplementary Tables 7 and 8). The determined dissociation constants (KD’s) at the recognition sites and nonspecific sites (tens and hundreds of nM, respectively) are consistent with literature12,21,33, further supporting the validity of our analyses. An interesting note here: for both CueR and ZntR, their affinity differences between recognition and nonspecific sites mainly come from kinetic differences in binding rather than unbinding (Supplementary Note 18.2).
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We acknowledge the National Institutes of Health (GM109993, GM106420 and AI117295) for funding, J. Xiao and P. Xu for gifts of mEos2 and mEos3.2 genes, X. Su, H. Lin, J. Peters, Y. Aye and C. Kinsland for helping with molecular biology and/or E. coli genetics.
The authors declare no competing financial interests.
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Chen, TY., Santiago, A., Jung, W. et al. Concentration- and chromosome-organization-dependent regulator unbinding from DNA for transcription regulation in living cells. Nat Commun 6, 7445 (2015). https://doi.org/10.1038/ncomms8445
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