Dielectric Trapping of Biopolymers Translocating through Insulating Membranes

Sensitive sequencing of biopolymers by nanopore-based translocation techniques requires an extension of the time spent by the molecule in the pore. We develop an electrostatic theory of polymer translocation to show that the translocation time can be extended via the dielectric trapping of the polymer. In dilute salt conditions, the dielectric contrast between the low permittivity membrane and large permittivity solvent gives rise to attractive interactions between the cis and trans portions of the polymer. This self-attraction acts as a dielectric trap that can enhance the translocation time by orders of magnitude. We also find that electrostatic interactions result in the piecewise scaling of the translocation time τ with the polymer length L. In the short polymer regime L≲10 nm where the external drift force dominates electrostatic polymer interactions, the translocation is characterized by the drift behavior τ∼L2. In the intermediate length regime 10nm≲L≲κb−1 where κb is the Debye–Hückel screening parameter, the dielectric trap takes over the drift force. As a result, increasing polymer length leads to quasi-exponential growth of the translocation time. Finally, in the regime of long polymers L≳κb−1 where salt screening leads to the saturation of the dielectric trap, the translocation time grows linearly as τ∼L. This strong departure from the drift behavior highlights the essential role played by electrostatic interactions in polymer translocation.


Introduction
The continuous improvement of our control over nanoscale physics allows an increasingly broader range of nanotechnological applications for bioanalytical purposes. Along these lines, the electrophoretic transport of biopolymers through nanopores can provide a surprisingly simple and fast approach for biopolymer sequencing [1][2][3][4][5][6][7]. This sequencing technique consists of mapping the nucleic acid structure of the translocating polymer from the ionic current signal caused by the molecule. At present, the translocation times provided by experiments are not sufficiently long for sensitive reading of this ionic current signal [6]. Thus, the technical challenge consists of reducing the polymer translocation speed by orders of magnitude from the current experimental values. Over the past two decades, this objective has motivated intensive research work with the aim to characterize the effect of various system characteristics on the polymer translocation dynamics.
Polymer translocation is driven by the entangled effects of electrostatic polymer-membrane interactions, the electrohydrodynamic forces associated with the electrophoretic and electroosmotic drags, and entropic barriers originating from conformational polymer fluctuations and hard-core polymer-membrane interactions. Due to the resulting complexity of the translocation process, polymer translocation models have initially separately considered the contribution from electrohydrodynamic and entropic effects. Within Langevin dynamics, theoretical studies of polymer translocation first focused on the role played by entropy [8][9][10][11][12] (see also Refs. [13,14] for an extended review of the literature). The contribution from electrostatics and hydrodynamics on the polymer translocation dynamics has been investigated by mean-field (MF) electrostatic theories [15][16][17][18]. Within a consistent electrohydrodynamic formulation, we have recently extended these translocation models by including beyond-MF charge correlations and direct electrostatic polymer-membrane interactions [19][20][21].
In the theoretical modeling of polymer translocation, the current technical challenge consists of incorporating on an equal footing conformational polymer fluctuations and electrostatic effects. The achievement of this difficult task would allow for unifying the entropic coarse-grained models and electrohydrodynamic theories mentioned above. At this point, it should be noted that such a unification necessitates the inclusion of polymer-membrane interactions outside the pore, while the translocation models of Refs. [19][20][21] developed for short polymers and long pores included exclusively the electrostatic polymer-membrane interactions inside the pore medium. In this work, we make the first attempt to overcome this limitation and develop a non-equilibrium theory of polymer translocation explicitly including the interactions between a charged dielectric membrane and an anionic polymer of arbitrary length. Within this theory, we characterize the effect of salt and membrane charge configurations, and the polymer length on the translocation dynamics of the molecule.
In Section 2, we introduce first the geometry and charge composition of the translocation model. Then, we derive the electrostatically augmented Fokker-Planck (FP) equation characterizing the translocation dynamics, and obtain the capture velocity and translocation time. Section 3.2 considers the effect of surface polarization forces on polymer translocation through neutral membranes. Therein, we identify a dielectric trapping mechanism enabling the extension of the translocation time by orders of magnitude. In Section 3.3, we investigate the effect of the fixed membrane charges on the dielectric trapping and reveal an electrostatic trapping mechanism occuring at positively charged membranes in contact with physiological salt concentrations. We also scrutinize in detail the effect of dielectric and electrostatic interactions on the scaling of the polymer translocation time with the polymer length. Our results are summarized in the Discussion part where the limitations of our model and future extensions are discussed.

Charge Composition of the System
The charge composition of the system is depicted in Figure 1. The membrane of thickness d, surface charge σ m of arbitrary sign, and dielectric permittivity ε m are immersed in the monovalent electrolyte NaCl of concentration ρ b and dielectric permittivity ε w = 80. We note in passing that, in our article, the dielectric permittivities are expressed in units of the vacuum permittivity ε 0 . Moreover, the membrane contains a pore oriented along the z-axis. The externally applied voltage between the cis and trans sides of the membrane induces a uniform electric field in the pore. This field exerts a constant force f 0 on the polymer portion enclosed by the nanopore. We note that the detailed formulation of the pore electrohydrodynamics would be necessary to relate quantitatively the force f 0 to the external electric field, the polymer charge, the ion density, and the electroosmotic flow. As this task is beyond the scope of the present work, the pore electrohydrodynamics will be coarse-grained and the drift effect on the polymer translocation will be described solely in terms of the driving force f 0 .
The polymer is modeled as a charged line of total length L, mass M, and the bare linear charge density of dsDNA molecules −λ c q with λ c = 2.0/(3.4 Å) and the electron charge q = 1.6 × 10 −19 C. Electrostatic polymer-membrane interactions induce an additional electrostatic force on the polymer charges. Appendix D explains the derivation of the corresponding electrostatic potential from the Debye-Hückel (DH) level electrostatic polymer grand potential. The latter is obtained by expanding the grand potential of the whole system at the quadratic order in the polymer charge [22]. In order to improve this approximation, we will make use of the variational charge renormalization technique [23] and evaluate the electrostatic polymer-membrane interactions in terms of the effective polymer charge densityλ c defined asλ c = nλ c . (1) The effective charge density (1) corresponds to the bare charge density λ c dressed by the counterion cloud around the polyelectrolyte. In Equation (1), n is the charge renormalization factor whose variational evaluation is explained in Appendix A. We finally note that, in the limit of vanishing salt ρ b → 0, the charge renormalization factor tends to its Manning limit n = 1/( B λ c ) [23] and the effective polymer charge (1) becomesλ where we used the Bjerrum length B = q 2 /(4πε w k B T) ≈ 7 Å, with the Boltzmann constant k B and the ambient temperature T = 300 K.

Modified Fokker-Planck Equation
The reaction coordinate of the translocation is the length s of the polymer portion on the trans side. The polymer portion on the cis side has length L − s (see Figure 1). Thus, in our model, the contribution from the pore length to the translocation dynamics is neglected and the right end of the polymer penetrating the membrane is assumed to reach immediately the trans side. This is a reasonable approximation for the present case of thin membranes and long polymers L d. This said, in the calculation of electrostatic polymer-membrane interactions, the finite thickness of the dielectric membrane will be fully taken into account.
The translocation dynamics is characterized by the Langevin equation where γ is the hydrodynamic friction coefficient. The first term on the r.h.s. of Equation (3) is the pore friction force and η p the pore friction coefficient. The second term is the total external force f (s) = −V p (s) acting on the polymer, with the polymer potential V p (s) including the effect of the externally applied electric force f 0 and electrostatic polymer-membrane interactions. Finally, the third term of Equation (3) corresponds to the Brownian force ξ(t). In the bulk electrolyte, the diffusion coefficient of a cylindrical molecule is given by [24] with the water viscosity η = 8.91 × 10 −4 Pa s, Euler's number e ≈ 2.718, and the DNA radius a = 1 nm. Thus, the corresponding hydrodynamic friction coefficient for the cylindrical molecule follows from Einstein's relation where λ m = M/L is the linear polymer mass density.
In Appendix B, we show that the effective FP equation associated with the Langevin Equation (3) is given by where c(s, t) is the polymer number density. In the dilute polymer regime where polymer-polymer interactions can be neglected, the function c(s, t) also corresponds to the polymer probability density. In Equation (6), the effective pore diffusion coefficient is given by with the net friction coefficient Finally, the effective polymer potential is

Capture Velocity v c and Translocation Time τ
We compute here the polymer translocation time τ corresponding to the time between the penetration of the polymer from the cis side and the exit of the molecule from the trans side, and the capture velocity v c characterizing the penetration speed of the molecule into the pore. To this end, we express Equation (6) as an effective diffusion equation with the polymer flux where the first and second terms on the r.h.s. correspond to the diffusive and convective flux components, respectively. We consider now the steady-state regime of the system characterized by a constant polymer flux J(s, t) = J st and density c(s, t) = c st (s). We recast Equation (11) in the form Next, we integrate Equation (12) by imposing an absorbing boundary condition (BC) c st (L) = 0 at the pore exit. The absorbing BC assumes that, due to the deep voltage-induced electric potential on the trans side, the polymer that completes its translocation is removed from the system at s = L. One obtains Setting s = 0 in Equation (13), one gets the characteristic polymer capture velocity corresponding to the inward polymer flux per reservoir concentration We note that Equation (14) corresponds to the characteristic speed at which the polymer reaches the minimum of the total electrostatic potential V p (z p ). In general, v c differs from the average translocation velocity. The capture and translocation velocities coincide only in the specific case of drift-driven translocation considered in Section 3.1.
In order to derive the translocation time, we first note that the polymer population in the pore follows from the integral of Equation (13) in the form The translocation time corresponds to the inverse translocation rate. The latter is defined as the polymer flux per total polymer number, i.e., τ −1 = J st /N p . This gives the polymer translocation time in the form In Appendix C, we show that Equation (16) can be also derived from the Laplace transform of the FP Equation (6) as the mean first passage time of the polymer from s = 0 to s = L.

Electrostatic Polymer Potential V p (s)
The electrostatic potential experienced by the polymer reads The first term on the r.h.s. of Equation (17) is the drift potential associated with the external force f 0 . The second term including the polymer grand potential ∆Ω p (s) accounts for electrostatic polymer-membrane interactions. In Appendix D, we show that this grand potential is given by The first term on the r.h.s. of Equation (18) corresponds to the direct interaction energy between the polymer and membrane charges, with the Gouy-Chapman length µ = 1/(2π B |σ m |) and DH screening parameter Then, the second term of Equation (18) corresponding to the sum of the individual self interaction energies of the polymer portions on the cis and trans sides reads where we defined the screening function p b = κ 2 b + k 2 and the dielectric jump function Finally, the interaction energy between the trans and cis portions of the polymer is

Drift-Driven Regime
The drift-driven regime corresponds to the case of high salt density or strong external force f 0 where polymer membrane interactions can be neglected, i.e., V p (s) ≈ − f 0 s. In the drift limit, the effective polymer potential (9) takes the downhill linear form βU p (s) = −λ 0 s where we introduced the characteristic inverse length λ 0 = β f 0 γ p /γ. The capture velocity (14) and translocation time (16) For strong electric forces with β f 0 L 1, Equations (22) and (23) take the standard drift form satisfying the drift-driven transport equation τ ≈ L/v c . Considering that the logarithmic term in Equation (4) is of order unity, and introducing the characteristic length L c = η p /(3πη), Equation (25) indicates that, for short polymers L L c , the translocation time exhibits a linear dependence on the polymer length, i.e., τ ≈ (η p / f 0 )L. For long polymers L L c , the translocation time grows quadratically with the polymer length as τ ≈ (λ m γ/ f 0 )L 2 . We note that these scaling laws also follow from the rigid polymer limit of the tension propagation theory [11].
We verified that the translocation dynamics is qualitatively affected by the pore friction only in the drift-driven regime considered above. Thus, in order to simplify the analysis of the model, from now on, we switch off the pore friction and set η p = 0. This yields, in Equations (8) and (9), γ p = γ. Consequently, the effective polymer potential in Equations (14) and (16)

Neutral Membranes: Dielectric Trapping
We investigate here the electrostatics of polymer translocation through neutral membranes. In silicon nitride membranes, the neutral surface condition is reached by setting the acidity of the solution to the isoelectric point value pH ≈ 5 [25]. In this limit where σ m = 0 and µ −1 = 0, the polymer-membrane coupling energy in the polymer potential (26) vanishes, i.e., Ω pm (s) = 0.

Dielectric Trapping of the Polymer in Dilute Salt
To scrutinize the effect of polarization forces on the capture and translocation dynamics, we consider the simplest situation where the polymer is dressed by its counterions, but there is no additional salt in the solvent, i.e., ρ b = 0. This corresponds to the limit κ b → 0 where the polymer self-energy components (20) and (21) become with the dielectric parameter ∆ 0 = (ε w − ε m )/(ε w + ε m ). According to Equations (26)-(28), in the limit of vanishing dielectric discontinuity ε m → ε w where ∆ 0 = 0, polymer-membrane interactions disappear and one recovers the drift behavior of Equations (24) and (25).
In Figure 2a,b, we display the polymer capture velocity v c and translocation time τ against the dimensionless external forcef 0 = β B f 0 at various membrane permittivities ε m ≤ ε w . One sees that, in the weak external force regimef 0 1, polarization effects arising from the low membrane permittivity result in the deviation of v c and τ from the linear response behavior of Equations (24) and (25). More precisely, the external force dependence of the translocation time switches from linear τ ∼ f −1 0 for large forcesf 0 1 to exponential ln τ ∼ − f 0 for weak forcesf 0 0.2 (see also the inset of Figure 2b). The exponential decay of τ with f 0 is the sign of the barrier-driven translocation that we scrutinize below. Figure 2a,b also show that, at fixed force f 0 , the dielectric discontinuity increases both the capture velocity v c and the translocation time τ from their drift values, i.e., ε m ↓ v c ↑ τ ↑. The mutual enhancement of v c and τ is an important observation for nanopore-based sequencing techniques whose efficiency depends on fast polymer capture and extended ionic current signal.
The mechanism behind the enhanced capture speed and translocation time is illustrated in Figure 3a,b. The plots display the electrostatic self-energy profiles, and the renormalized polymer potential U p (s) − U p (0) that includes the electric force f 0 and determines the capture velocity (14) and translocation time (16). First, we note that the self-energy component ∆Ω intra (s) is concave and repulsive (dotted curves in Figure 3a). Thus, the individual image-charge interactions of the cis and trans portions of the polymer act as an electrostatic barrier limiting the polymer capture by the pore. Then, one sees that the energy component ∆Ω inter (s) is convex and negative (dashed curves). Hence, the dielectric coupling between the cis and trans portions gives rise to an attractive force that favors the capture of the molecule. In the present dilute salt conditions, the trans-cis coupling takes over the repulsive image-charge interactions. This gives rise to a purely convex and attractive total interaction potential ∆Ω p (s) whose slope is enhanced with the magnitude of the dielectric discontinuity, i.e., ε m ↓ |∆Ω p (s)| ↑ (compare the solid curves in Figure 3a). Figure 3b shows that, as a result of this additional electrostatic force, the polymer potential develops an attractive well whose depth increases with the strength of the dielectric discontinuity, ε m ↓ U p (s) − U p (0) ↓. This dielectrically induced potential well speeds up the polymer capture but also traps the polymer at its minimum, resulting in the mutual enhancement of the polymer capture speed and translocation time in Figure 2a,b.
In order to localize the position of the dielectric trap, we pass to the asymptotic insulator limit ε m = 0 where the grand potential components (27) and (28) can be evaluated analytically as β∆Ω intra (s) = ln(2)L/ B and within this approximation, the solution of the equation U p (s * ) = 0 shows that the position of the trap rises linearly with the force f 0 and the polymer length L as Equation (30) can be useful to adjust the location of the dielectric trap in translocation experiments.

Effect of Polymer Length and Finite Salt Concentration
We scrutinize here the alteration of the polymer translocation time and capture speed by the polymer length and salt concentration. Figure 4a shows that, at a given salt concentration, the length dependence of the translocation time is characterized by three regimes. At short polymer lengths L < L − where L − ≈ 10 nm corresponds to the upper boundary of the drift-driven translocation regime, polymer-membrane interactions and the self-energy ∆Ω p (s) are weak, and the translocation is characterized by drift transport, i.e., τ ≈ τ dr . Consequently, the translocation time of short polymers rises quadratically with the molecular length, i.e.,  The departure from drift transport occurs at intermediate lengths L > L − . In this regime, the magnitude of the attractive trans-cis coupling becomes significant and the increase of the polymer length strongly enhances the depth of the electrostatic potential trap (see Figure 4b). Figure 4a shows that this results in the amplification of the translocation time with the polymer length by orders of magnitude. We found that this trend is the reminiscent of an exponential growth ln τ ∝ L reached in the asymptotic insulator limit ε m = 0 (data not shown).
The quick rise of the translocation time with the polymer length continues up to the characteristic length L ≈ L + = κ −1 b whose numerical value is given in the caption of Figure 4. L + corresponds to the critical polymer length beyond which electrostatic polymer-membrane interactions saturate. More precisely, due to salt screening, the trans-cis portions of the polymer separated by a distance larger than L + interact weakly. As a result, the depth of the dielectric trap is mostly invariant by the extension of the polymer length beyond L + (see Figure 4b). Thus, for L L + , the value of the double integral in Equation (16) is not significantly affected by the length L, i.e., τ ∝ D −1 p ∝ L. This results in the linear rise of the translocation time with the polymer length (see also the inset of Figure 4a), i.e., We note that the scaling discussed above qualitatively agrees with experiments on α-Hemolysin pores exhibiting a similar piecewise length dependence of the translocation time (see, e.g., Figure 9 of Ref. [26]). Finally, Figure 4 shows that, due to the screening of dielectric polymer-membrane interactions, added salt reduces the translocation time, i.e., ρ b ↑ τ ↓. Beyond the characteristic salt concentration ρ b ≈ 10 −4 M where the length L + approaches L − , the translocation time tends to its drift limit at all polymer lengths.

Charged Membranes
We investigate here the alteration of the features discussed in Section 3.2 by a finite membrane charge. For a positive membrane charge σ m ≥ 0 corresponding to acidity values pH 5 [25], the direct polymer-membrane coupling energy (19) results in an attractive force favoring the polymer capture. In order to characterize the effect of this additional force on the dielectric trapping mechanism, we first focus on the dilute salt regime and set ρ b = 10 −4 M. Figure 5a-c display the capture velocity, translocation time, and renormalized polymer potential at various weak membrane charge densities including the case of neutral membranes (navy curves).
One first notes that, upon the increase of the cationic membrane charge, the onset of the polymer-membrane attraction significantly deepens the trapping potential U p (s) − U p (0). This enhances the translocation time of long polymers by orders of magnitude, i.e., σ m ↑ τ ↑ for L 30 nm. However, one also sees that, at the beginning of the translocation corresponding to the polymer capture regime s 0.2 L, the slope of the polymer potential is weakly affected by the increment of the membrane charge density. As a result, the dielectrically enhanced capture velocity v c remains practically unaffected by a weak membrane charge. Finally, Figure 5b shows that the linear scaling of the translocation time with the polymer length remains unchanged by the surface charge, i.e., τ ∝ L for L L + (see also the inset). One however notes that the finite membrane charge shifts the regime of linearly rising translocation time to larger polymer lengths, i.e., σ m ↑ L + ↑.
We consider now the stronger salt regime where the dielectric trapping effect disappears. To simplify the numerical computation of the capture velocity Equation (14) and translocation time Equation (16), we neglect the dielectric interaction terms of Equation (26) that become perturbatively small. Within this approximation, the polymer potential becomes U p (s) ≈ − f 0 s + Ω pm (s). Figure 6a-c show that, in the regime of moderate salt concentration and cationic membrane charge (purple and red curves), the direct polymer-membrane charge attraction can solely induce a deep enough electrostatic trap to enhance both the capture velocity and the translocation time by orders of magnitude, i.e., σ m ↑ v c ↑ τ ↑. In terms of the dimensionless constant c = βµκ b f 0 /(4λ c ), the relation U p (s * ) = 0 yields the location of the electrostatic trap in the form Equation (33) can enable to control the position of the polymer trap by changing the relative weight of the drift force f 0 and the electrostatic polymer-membrane attraction via the adjustment of various system parameters. Indeed, in the regime βµκ b f 0 /(4λ c ) 1 corresponding to weak salt or external force f 0 , and high membrane charge σ m and/or polymer chargeλ c , Equation (33) indicates the trapping of the polymer at s * ≈ L/2. Moving to the opposite regime βµκ b f 0 /(4λ c ) 1 of strong salt or external force, low membrane or polymer charge strength, and long polymers κ b L 1, the trapping point in Equation (33) is shifted towards the polymer exit s * = L according to the relation Figure 6b also shows that, at strong enough membrane charges (red curve), the trapping-induced enhancement of the translocation time is followed at large lengths by the linear scaling behavior τ ∝ L equally observed for neutral and weakly charged membranes (see the inset of Figure 6c). At intermediate charges, the system tends to the drift behavior τ → τ dr before the linear scaling regime is reached (purple curve in Figure 6b). We also note that, in the short length regime of Figure 6b, the weak curvature of the drift translocation time τ dr stems from the logarithmic correction factor in the polymer diffusion coefficient of Equation (4).  We finally investigate the effect of anionic membrane charges reached in the acidity regime pH 5. Interestingly, Figure 6b indicates that, in strong salt conditions where the polymer-membrane charge coupling dominates the dielectrically induced polymer self-interactions, the enhancement of the translocation time in Equation (16) does not depend on the sign of the membrane charge, i.e., τ(σ m ) = τ(−σ m ). However, one also notes that, in anionic membranes, the like-charge polymer-membrane repulsion gives rise to an electrostatic barrier at the pore entrance (see Figure 6c). Figure 6a shows that this barrier diminishes the polymer capture rate by several orders of magnitude, i.e., |σ m | ↑ U p (s) − U p (0) ↑ v c ↓ for σ m < 0. Thus, in anionic membranes, the enhancement of the translocation time stems from the suppression of polymer capture by the electrostatic polymer-membrane repulsion. The existence of a similar barrier induced by electrostatic DNA-pore repulsion has been previously identified by a different polymer translocation model developed for long nanopores and short polymers [20].

Discussion
The accurate characterization of voltage-driven polymer translocation requires modeling of this process by including the electrostatic details of the polymer-membrane complex and the surrounding electrolyte solution. Motivated by this need, we have developed here an electrostatic transport model to investigate the effect of surface polarization forces, added salt, and membrane charge on the capture and translocation of stiff polymers with arbitrary length. Our results are summarized below.
We first considered the case of neutral membranes and dilute salt regime where the polyelectrolyte is dressed by its counterions, but there is no additional salt in the system. In this regime, we identified a dielectrically induced polymer trapping mechanism. Namely, the dielectric contrast between the low permittivity membrane and large permittivity solvent leads to attractive interactions between the cis and trans portions of the polymer. The attraction gives rise to a dielectric trap located at s = s * = [L + (d + L/2)f 0 ]/2. The trap speeds up the polymer capture occurring at s < s * but slows down the escape of the polymer at s > s * , amplifying the polymer capture velocity by several factors and the total translocation time by orders of magnitude.
We also observed that, in neutral membranes, added salt of concentration ρ b 10 −4 M suppresses the dielectric trapping of the polymer. However, at arbitrary salt densities, positive membrane surface charges emerging at low solution pH restore the polymer trapping via the electrostatic polymer-membrane attraction. This electrostatic trap can enhance the polymer capture speed and translocation time as efficiently as its dielectric counterpart. It was also shown that the location of the trap in Equation (33) can be adjusted by modifying the experimentally accessible model parameters such as the salt and membrane charge density. Thus, the electrostatic trapping can equally well provide an efficient way to extend the duration of the ionic current blockade required for the sensitive sequencing of the translocating biopolymer.
Finally, we investigated the effect of polymer trapping on the scaling of the translocation time with the polymer length. At short lengths L 10 nm where the interactions between the cis and trans sides of the polymer are dominated by the drift force f 0 , the translocation is characterized by the drift behavior of Equation (25). In the intermediate polymer length regime 10 nm where the attractive trans-cis coupling takes over the drift force, the resulting dielectric trap leads to a quasi-exponential inflation of the translocation time with the length of the molecule. Beyond the characteristic polymer length L ≈ κ −1 b where ionic screening comes into play, the depth of the dielectric trap becomes saturated. As a result, the translocation time of long polymers rises linearly with the molecular length, i.e., τ ∝ L. We finally showed that, in positively charged membranes, the electrostatic trap results in a similar piecewise length dependence of the translocation time. It is also important to note that such a piecewise trend has been previously observed in translocation experiments with α−Hemolysin pores [26].
The present formalism developed for long polymers and thin membranes is complementary to our previous translocation model of Ref. [20] introduced for short polymers translocating through long nanopores. These two formalisms can be unified in the future by taking into account both the detailed electrohydrodynamics of the nanopore and electrostatic polymer-membrane interactions outside the pore. This extension would also enable considering the influence of nonlinear electrostatic correlation effects such as polymer and pore charge inversion on the translocation dynamics [19].
Before concluding, we would like to comment about the stiff polymer approximation of the model. Considering the DNA persistence length l p ∼ 50 nm at the salt density ρ b = 0.1 M, the entropic polymer fluctuations neglected in our model should become relevant for polymers of length L 50 nm. Thus, in the corresponding long polymer regime, the resulting entropic cost for polymer capture is expected to enhance the polymer translocation times and reduce the capture velocities from the predictions in Figure 6a,b. It should be, however, noted that as the remaining results reported in Figures 2-5 were obtained in the dilute electrolyte regime ρ b ≤ 5 × 10 −4 M where DNA is stiffer than at the physiological salt density ρ b = 0.1 M, our main conclusions should be qualitatively unaffected by the rigid rod approximation. A quantitatively accurate evaluation of the error caused by the stiff polymer approximation requires the direct inclusion of entropic polymer fluctuations into our model. This formidable task is beyond the scope of the present article. The consideration of this extension in a future work may also allow for incorporating into our electrostatic formalism the tension propagation mechanism relevant for long polymers [10,14]. Funding: This research was funded by the Academy of Finland QTF Centre of Excellence program (project 312298).

Conflicts of Interest:
The authors declare no conflict of interest.
To progress further, we express the noise-averaged definition of the probability density where the term δs on the r.h.s. corresponds to the random displacement over the infinitesimal time interval δt. Next, we Taylor-expand the corresponding term at order O δs 2 to obtain c(s, t + δt; s , t) = 1 + δs ∂ s + 1 2 Inserting Equation (A12) into Equation (A10), carrying out integrations by parts, and using the relations (A8) and (A9), one obtains where we introduced the effective diffusion coefficient Taylor-expanding the l.h.s. of Equation (A12), one gets Equating the relations (A12) and (A15) and simplifying the result, one finally obtains the modified FP equation including the effective polymer potential

Appendix C. Calculation of the Translocation Time
Here, based on the FP Equation (A16), we derive the polymer translocation time (15) as the mean first passage time of the polymer from the cis to the trans side. Our derivation will follow the approach of Ref. [29] that will be extended to the presence of a steady-state solution to the FP equation. The BCs associated with this equation are the initial condition at the pore mouth and an absorbing boundary at the pore exit, The probability of polymer survival in the pore is The translocation probability can be thus expressed as P tr (t) = 1 − S(t) and the mean-first passage time distribution is therefore ψ(t) = P tr (t) = −S (t), or where we defined Y 0 (s) = Y(s, q = 0). According to Equation (A24), given the initial condition (A18), the Laplace transform Y 0 (s) solves the differential equation

Appendix D. Derivation of the Polymer Interaction Potential ∆Ω p (s)
In this appendix, we explain the calculation of the polymer-membrane interaction potential ∆Ω p (s) in Equation (17) from the total polymer grand potential Ω p (s) = Ω pm (s) + Ω s (s).
In Equation (A31), the term Ω pm (s) is the interaction energy between the polymer and membrane charges. The second component Ω s (s) corresponds to the polymer self-energy accounting for the polarization forces induced by the dielectric contrast between the membrane and the solvent. Below, we review briefly the computation of these two potential components previously derived in Ref. [22]. The electrostatic potential ∆Ω p (s) will be obtained from the grand potential (A31) at the end of Appendix D.2.
two-dimensional wave vector k. In order to simplify the notation, the k−dependence of these functions will be omitted.
The net interaction potential ∆Ω p (s) between the polymer and the charged dielectric membrane corresponds to the grand potential (A31) minus its bulk value. In the bulk reservoir where there is no charged interface, i.e., σ m = 0, the polymer-membrane charge coupling energy (A38) naturally vanishes. Consequently, the interaction potential becomes ∆Ω p (s) = Ω pm (s) + ∆Ω s (s), where the polymer self-energy renormalized by its bulk value is Using Equations (A45)-(A48) in Equation (A51), after lengthy algebra, the self-energy Equation (A51) becomes ∆Ω s (s) = ∆Ω intra (s) + ∆Ω inter (s), with the individual self-energy of the polymer portions on the cis and trans sides of the membrane β∆Ω intra (s) = Bλ