Team:Groningen/Modelling/Arsenic

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Revision as of 10:12, 6 October 2009

Based on the quasi-steady-state derivation below we have made the simplified version of our model shown below. The simplification is based on two key assumptions (which are also illustrated below, next to the table "Breakdown of core substances"):

• Binding and unbinding of arsenic to/from the transporters occurs on a much smaller time scale than changes in the concentration of arsenic inside and outside the cell. And similarly, we assume that (un)binding of ArsR to/from the ars promoter is much faster than the production of ArsR (for example).
• The concentration of transporters is insignificant compared to the concentration of arsenic inside and outside the cell, and similarly for the concentration of ars promoters compared to the concentration of ArsR. The concentration of promoters might not be insignificant.

This leads to the Michaelis-Menten equation for import, but also some more general equations for export using ArsB and accumulation with ArsR (for example, the Hill equation can be recognized in the activity of the ars promoter).

A schematic representation of the processes involved in arsenic filtering (keep in mind that ArsR represses the expression of the genes behind ars). Note that MBPArsR and fMT are not shown for clarity.

Breakdown of core substances Core substance Component Relative abundance ArsBT ArsB K7 ArsBAs As(III)in As(III)inT As(III)in KRd ArsRAs ArsR arsT ars K3d² ArsRars ArsR² ars ars1 ars1T ars2 ars2T ArsRT ArsR KRd ArsRAs As(III)in

Circles correspond to core substances. We consider the reactions between the overlapping substances so fast that we model them by determining the ratios between the substances when the reactions between them are in equilibrium. Also, the complexes formed with ars, GlpF and ArsB (the small circles) are considered to have such a low concentration that they are of no importance to the concentrations of As(III)in/-ex and ArsR (the large circles).

The raw model

The following variables play an important role in our system (these can be concentrations of substances, the density of the cell, etc.):

• Extracellular:
  • As(III)_ex
• Membrane (all naturally occurring, but we plan to bring GlpF to overexpression):
  • GlpF (concentration w.r.t. the exterior of the cell)
  • GlpF_As (concentration w.r.t. the exterior of the cell)
  • ArsB (concentration w.r.t. the interior of the cell)
  • ArsB_As (concentration w.r.t. the interior of the cell)
• Intracellular (ars2, pro and GV are introduced):
  • As(III)_ex
  • ars1 (concentration of unbound promoters naturally occurring in E. coli)
  • ars2 (concentration of unbound promoters in front of gas vesicle genes)
  • proR (concentration of constitutive promoters in front of arsR)
  • proM (concentration of constitutive promoters in front of mbp-arsR)
  • proF (concentration of constitutive promoters in front of fMT)
  • ArsR
    ArsR binds to ars to repress production of the genes they regulate, and binds to As(III) to make it less of a problem for the cell.

     i 
  • ArsR_As (bound to As(III))
  • ArsR_ars1 (bound to ars1)
  • ArsR_ars2 (bound to ars2)
  • MBPArsR
    A fusion of maltose binding protein and ArsR.

     i 
  • MBPArsR_As (bound to As(III))
  • fMT
  • fMT_As (bound to multiple As(III))
  • ArsR_As (bound to As(III))
  • GV (concentration of gas vesicles)

The variables above can be related to each other through the following "reactions" (color coding is continued below to show which parts of the differential equations refer to which groups of reactions):

• Transport (based on Rosen1996, Meng2004 and Rosen2009)
  • As(III)_ex + GlpF ↔ GlpF_As
  • GlpF_As → GlpF + As(III)
  • As(III)_in + ArsB ↔ ArsB_As
  • ArsB_As → ArsB + As(III)_ex
  • ArsB → null (degradation)
• Accumulation (mostly based on Chen1997)
  • As(III)_in + ArsR ↔ ArsR_As
  • As(III)_in + MBPArsR ↔ MBPArsR_As
  • n_f As(III)_in + fMT ↔ fMT_As
  • ars1 + 2 ArsR ↔ ArsR_ars1
  • ars2 + 2 ArsR ↔ ArsR_ars2
  • ars1 → ars1 + ArsR + ArsB (transcription + translation)
  • ars2 → ars2 + GV (transcription + translation)
  • proR → proR + ArsR (transcription + translation)
  • proM → proM + MBPArsR (transcription + translation)
  • proF → proF + fMT (transcription + translation)
  • ArsR → null (degradation)
  • GV → null (degradation)

Resulting in the following differential equations (please note that some can be formed by linear combinations of the others), using color coding to show the correspondence to the reactions above:

• (d/dt) As(III)_ex = - (d/dt) GlpF_As - k6 GlpF_As + (Vc/Vs) k8 ArsB_As
• (d/dt) GlpF = - (d/dt) GlpF_As
• (d/dt) GlpF_As = k5_on As(III)_ex GlpF - (k5_off+k6) GlpF_As
• (d/dt) ArsB = - (d/dt) ArsB_As + β4 ars1 - ln(2)/τB ArsB
• (d/dt) ArsB_As = k7_on As(III)_in ArsB - (k7_off+k8) ArsB_As
• (d/dt) As(III)_in = - (d/dt) ArsR_As - (d/dt) MBPArsR_As - n_f (d/dt) fMT_As - (d/dt) ArsB_As - k8 ArsB_As + (Vs/Vc) k6 GlpF_As
• (d/dt) ars1 = - (d/dt) ArsR_ars1
• (d/dt) ars2 = - (d/dt) ArsR_ars2
• (d/dt) ArsR = βRN ars1 + βR proR - (ln(2)/τR) ArsR - (d/dt) ArsR_As - 2 (d/dt) ArsR_ars1 - 2 (d/dt) ArsR_ars2
• (d/dt) ArsR_As = kR_on ArsR As(III)_in - kR_off ArsR_As
• (d/dt) ArsR_ars1 = k3_on ArsR² ars1 - k3_off ArsR_ars1
• (d/dt) ArsR_ars2 = k3_on ArsR² ars2 - k3_off ArsR_ars2
• (d/dt) MBPArsR = βM proM - (ln(2)/τM) MBPArsR - (d/dt) MBPArsR_As
• (d/dt) MBPArsR_As = kM_on MBPArsR As(III)_in - kM_off MBPArsR_As
• (d/dt) fMT = βF proF - (ln(2)/τF) fMT - (d/dt) fMT_As
• (d/dt) fMT_As = kF_on fMT As(III)_in^n_f - kF_off fMT_As
• (d/dt) GV = βG ars2 - ln(2)/τG GV

Using the following constants/definitions:

See Chen1997 for the interplay between ArsR and ArsD (the latter has a role similar to ArsR, but we do not treat it, as it is not present in our system).

Quasi steady state

First of all, we assume the concentration of transporters is quite low compared to the concentration of the transported substances. After all, if this were not the case the transporters would act more like "storage" proteins than transporters (note that this can be even more rigorously justified if, for example, GlpFT<<K5). Similarly, there will generally only be a few ars promoters, compared to very many ArsR molecules. This leads to:

As(III)exT ≈ As(III)ex
As(III)inT ≈ As(III)in + ArsRAs + MBPArsRAs + fMTAs
ArsRT ≈ ArsR + ArsRAs

Also, we assume the binding and unbinding of molecules to the transporters occurs on a much finer time-scale than any actual changes to the concentrations inside and outside the cell. Similarly, within the cell we assume diffusion processes are very fast and binding/unbinding of substances is quite fast compared to the production of proteins. This leads us to assume that the following ratios between substances are constantly in equilibrium:

arsT = ars + ArsRars
ars1 / ars1T = ars2 / ars2T

 ars = ars1 + ars2
 ars = ars1 (1 + ars2T / ars1T)
ars1 = ars / (1 + ars2T / ars1T)
ars1 = ars ars1T / arsT

ars2 = ars ars2T / arsT

As(III)ex : GlpFAs ≈ As(III)ex : 0
GlpF : GlpFAs
ArsB : ArsBAs
As(III)in : ArsRAs : MBPArsRAs : fMTAs : ArsBAs ≈ As(III)in : ArsRAs : MBPArsRAs : fMTAs : 0
ArsR : ArsRAs : 2 ArsRars ≈ ArsR : ArsRAs : 0
ars : ArsRars

To determine what the unknown ratios are we can set the following derivatives to zero (these are the derivatives of the complexes corresponding to the four overlapping regions in the diagram):

0 = (d/dt) GlpFAs = k5on As(III)ex GlpF - (k5off+k6) GlpFAs
0 = (d/dt) ArsBAs = k7on As(III)in ArsB - (k7off+k8) ArsBAs
0 = (d/dt) ArsRars = k3on ArsR² ars - k3off ArsRars
0 = (d/dt) ArsRAs = kRon ArsR As(III)in - kRoff ArsRAs
0 = (d/dt) MBPArsRAs = kMon MBPArsR As(III)in - kMoff MBPArsRAs
0 = (d/dt) fMTAs = kFon fMT As(III)in^nf - kFoff fMTAs

The first two derivates let us determine the ratios between bound and unbound transporters:

0 = (d/dt) GlpFAs = k5on As(III)ex GlpF - (k5off+k6) GlpFAs

k5on As(III)ex GlpF = (k5off+k6) GlpFAs
               GlpF = (k5off+k6)/k5on GlpFAs / As(III)ex
               GlpF = K5 GlpFAs / As(III)ex

                 GlpF : GlpFAs
K5 GlpFAs / As(III)ex : GlpFAs
                   K5 : As(III)ex

0 = (d/dt) ArsBAs = k7on As(III)in ArsB - (k7off+k8) ArsBAs

k7on As(III)in ArsB = (k7off+k8) ArsBAs
               ArsB = (k7off+k8)/k7on ArsBAs / As(III)in
               ArsB = K7 ArsBAs / As(III)in

                 ArsB : ArsBAs
K7 ArsBAs / As(III)in : ArsBAs
                   K7 : As(III)in

The next two differential equations can be used to determine the relative abundances of ArsR and ArsRAs, and ars and ArsRars:

0 = (d/dt) ArsRAs = kRon ArsR As(III)in - kRoff ArsRAs

kRon ArsR As(III)in = kRoff ArsRAs
           ArsRAs = kRon/kRoff ArsR As(III)in
           ArsRAs = ArsR As(III)in / KRd

ArsR : ArsRAs
ArsR : ArsR As(III)in / KRd
KRd  : As(III)in

0 = (d/dt) ArsRars = k3on ArsR² ars - k3off ArsRars

k3on ArsR² ars = k3off ArsRars
       ArsRars = k3on/k3off ArsR² ars
       ArsRars = ArsR² ars / K3d²

ars : ArsRars
ars : ArsR² ars / K3d²
K3d² : ArsR²

For MBPArsR and fMT we find:

0 = (d/dt) MBPArsRAs = kMon MBPArsR As(III)in - kMoff MBPArsRAs

MBPArsR : MBPArsRAs = KMd : As(III)in

0 = (d/dt) fMTAs = kFon fMT As(III)in^nf - kFoff fMTAs

fMT : fMTAs = KFd^nf : As(III)in^nf

And finally the relative abundances of arsenic:

ArsRAs = ArsR As(III)in / KRd

As(III)in : ArsRAs               : MBPArsRAs               : fMTAs
As(III)in : ArsR As(III)in / KRd : MBPArsR As(III)in / KMd : fMT As(III)in^nf / KFd^nf
1         : ArsR / KRd           : MBPArsR / KMd           : fMT As(III)in^(nf-1) / KFd^nf

Summarizing:

As(III)ex : GlpFAs ≈ As(III)ex : 0
GlpF : GlpFAs = K5 : As(III)ex
ArsB : ArsBAs = K7 : As(III)in
As(III)in : ArsRAs : MBPArsRAs : fMTAs ≈ 1 : ArsR / KRd : MBPArsR / KMd : fMT As(III)in^(nf-1) / KFd^nf
ars : ArsRars = K3d² : ArsR²
ArsR : ArsRAs ≈ KRd : As(III)in
MBPArsR : MBPArsRAs = KMd : As(III)in
fMT : fMTAs = KFd^nf : As(III)in^nf

Now we can look at the differential equations for the totals of ArsB (so ArsBT=ArsB+ArsBAs), ArsR, As(III)in and As(III)ex (GlpFT and arsT are assumed to be constant):

(d/dt) As(III)exT = (d/dt) As(III)ex + (d/dt) GlpFAs
                  = - (d/dt) GlpFAs - k6 GlpFAs + (Vc/Vs) k8 ArsBAs + (d/dt) GlpFAs
                  = (Vc/Vs) k8 ArsBAs - k6 GlpFAs
                  = (Vc/Vs) k8 ArsBAs - (Vc/Vs) v5 GlpFAs / GlpFT
                  = (Vc/Vs) k8 ArsBAs - (Vc/Vs) v5 As(III)ex / (K5+As(III)ex)
                  = (Vc/Vs) k8 ArsBAs - (Vc/Vs) v5 As(III)exT / (K5+As(III)exT)
(d/dt) ArsBT = (d/dt) ArsB + (d/dt) ArsBAs
             = - (d/dt) ArsBAs + βB ars1 - ln(2)/τB ArsB + (d/dt) ArsBAs
             = βB ars1 - ln(2)/τB ArsB
(d/dt) As(III)inT = -(Vs/Vc) (d/dt) As(III)exT
                  = v5 As(III)exT / (K5+As(III)exT) - k8 ArsBT As(III)in / (K7+As(III)in)
(d/dt) ArsRT = (d/dt) ArsR + (d/dt) ArsRAs + 2 (d/dt) ArsRars
             = βRN ars1 + βR proR - (ln(2)/τR) ArsR - (d/dt) ArsRAs - 2 (d/dt) ArsRars + (d/dt) ArsRAs + 2 (d/dt) ArsRars
             = βRN ars1 + βR proR - (ln(2)/τR) ArsR
(d/dt) MBPArsRT = (d/dt) MBPArsR + (d/dt) MBPArsRAs
                = βM proM - (ln(2)/τM) MBPArsR
(d/dt) fMTT = (d/dt) fMT + (d/dt) fMTAs
            = βF proF - (ln(2)/τF) fMT

Steady state

By looking at the steady state of the system we can say something about its long-term behaviour. This also makes it easier to analyze relations between variables. To derive the steady state solution we take the quasi steady state solution and simplify it further by setting additional derivatives to zero:

0 = (d/dt) ArsBT = βB ars1 - ln(2)/τB ArsB
0 = (d/dt) As(III)inT = v5 As(III)exT / (K5+As(III)exT) - k8 ArsBAs
0 = (d/dt) ArsRT = βRN ars1 + βR pro - (ln(2)/τR) ArsR
0 = (d/dt) GV = βG ars2 - ln(2)/τG GV

This directly leads to:

   0 = βB ars1 - ln(2)/τB ArsB
ArsB = βB (τB/ln(2)) ars1
ArsB = βB (τB/ln(2)) ars1T K3d²/(K3d²+ArsR²)

 0 = βG ars2 - ln(2)/τG GV
GV = βG (τB/ln(2)) ars2
GV = βG (τB/ln(2)) ars2T K3d²/(K3d²+ArsR²)

For the intra- and extracellular concentrations we can find the following condition:

0 = v5 As(III)exT / (K5+As(III)exT) - k8 ArsBAs
0 = v5 As(III)exT / (K5+As(III)exT) - k8 ArsB As(III)in / K7
0 = v5 As(III)exT / (K5+As(III)exT) - k8 ArsB As(III)inT / (K7 (1+ArsR/KRd))
0 = v5 As(III)exT (K7(1+ArsR/KRd)) - k8 ArsB As(III)inT (K5+As(III)exT)
0 = v5 K7 (1+ArsR/KRd) As(III)exT - k8 ArsB K5 As(III)inT - k8 ArsB As(III)exT As(III)inT

     As(III)T = Vs As(III)exT + Vc As(III)inT
Vs As(III)exT = As(III)T - Vc As(III)inT

0 = v5 K7 (1+ArsR/KRd) As(III)exT - k8 ArsB K5 As(III)inT - k8 ArsB As(III)exT As(III)inT
0 = v5 K7 (1+ArsR/KRd) Vs As(III)exT - k8 ArsB Vs K5 As(III)inT - k8 ArsB Vs As(III)exT As(III)inT
0 = v5 K7 (1+ArsR/KRd) (As(III)T - Vc As(III)inT) - k8 ArsB Vs K5 As(III)inT - k8 ArsB (As(III)T - Vc As(III)inT) As(III)inT
0 = v5 K7 (1+ArsR/KRd) As(III)T - v5 Vc K7 (1+ArsR/KRd) As(III)inT - k8 ArsB Vs K5 As(III)inT - k8 ArsB As(III)T As(III)inT + k8 ArsB Vc As(III)inT²
0 = v5 K7 (1+ArsR/KRd) As(III)T - (v5 Vc K7 (1+ArsR/KRd) + k8 ArsB Vs K5 + k8 ArsB As(III)T) As(III)inT + k8 ArsB Vc As(III)inT²
0 = v5 K7 (1+ArsR/KRd) As(III)T - (v5 Vc K7 (1+ArsR/KRd) + k8 ArsB (Vs K5 + As(III)T)) As(III)inT + k8 ArsB Vc As(III)inT²

As(III)inT = (b - √(b² - 4 a c))/(2 a)
           = 2 c/(b + √(b² - 4 a c))
         a = k8 ArsB Vc
         b = v5 Vc K7 (1+ArsR/KRd) + k8 ArsB (Vs K5 + As(III)T)
         c = v5 K7 (1+ArsR/KRd) As(III)T

Finally, for ArsR we can find the following third-order equation:

0 = βRN ars1 + βR pro - (ln(2)/τR) ArsR
0 = βRN ars1T K3d²/(K3d²+ArsR²) + βR pro - (ln(2)/τR) ArsR
0 = βRN ars1T K3d² + βR pro (K3d²+ArsR²) - (ln(2)/τR) ArsR (K3d²+ArsR²)
0 = βRN ars1T K3d² + βR pro K3d² + βR pro ArsR² - (ln(2)/τR) ArsR K3d² - (ln(2)/τR) ArsR³
0 = (βRN ars1T + βR pro) K3d² - (ln(2)/τR) K3d² ArsR + βR pro ArsR² - (ln(2)/τR) ArsR³
0 = (βRN ars1T + βR pro) (τR/ln(2)) K3d² - K3d² ArsR + βR (τR/ln(2)) pro ArsR² - ArsR³

According to Mathematica's solution of Reduce[eq && K3d > 0 && arsT >= 0 && pro >= 0 && β1 > 0 && β3 > 0 && τR > 0, ArsR, Reals] (where eq is the equation shown above) there is only one real solution (examining the discriminant of eq confirms this), so we can solve the equation safely using Newton's (or Halley's) method.