Difference between revisions of "Binding of R2 to A"

From ISMOC
Jump to: navigation, search
(Parameters)
(Parameters)
Line 45: Line 45:
 
| <math>630 s^{-1}</math>
 
| <math>630 s^{-1}</math>
 
(Range tested: <math>0-10^{3} s^{-1}</math>)
 
(Range tested: <math>0-10^{3} s^{-1}</math>)
 +
 
(Bistability range: <math>460-630 s^{-1}</math>)
 
(Bistability range: <math>460-630 s^{-1}</math>)
 
|According to Northrup et al. the <math>K_{a}</math> of protein-protein bond formations occur in the order of <math>10^{6} M^{-1}s^{-1}</math>, this value is used to calculate the dissociation rate for the ScbR-ScbA binding. Therefore the range of the <math>k^{-}_{3}</math> values is calculated as per <math>k^{-}_{3}=K_{d3} \cdot K_{a}</math>.
 
|According to Northrup et al. the <math>K_{a}</math> of protein-protein bond formations occur in the order of <math>10^{6} M^{-1}s^{-1}</math>, this value is used to calculate the dissociation rate for the ScbR-ScbA binding. Therefore the range of the <math>k^{-}_{3}</math> values is calculated as per <math>k^{-}_{3}=K_{d3} \cdot K_{a}</math>.

Revision as of 17:55, 12 October 2015

The ScbR homo-dimer (R2) forms a complex with ScbA (A).

Go back to overview
About this image

Chemical equation

A + R_{2} \rightleftharpoons A-R_{2}

Rate equation

 r= \frac{k^{-}_{3}}{K_{d3}}\cdot [A]\cdot [R_{2}] - k^{-}_{3}\cdot [A-R_{2}]

Parameters

The parameters of this reaction are the dissociation constant for binding of ScbR to ScbA (K_{d3}) and the dissociation rate for binding of ScbR to ScbA (k^{-}_{3}). Since there is no concrete evidence of the existence of the ScbA-ScbR complex so far, it is possible that the interaction between the two proteins is unstable/ transient and therefore the parameter values reflect this belief. The values of such complexes according to the literature [1] , lie in the millimolar or micromolar scale.

  • Ozbabacan et al. 2011[1]
  • Perkins et al. 2010[2]
Name Value Units Value in previous GBL model [3] Remarks-Reference
K_{d3} 10^{3}-10^{6} [1] nM 0.083 nM^{-1} s^{-1}

(Range tested: 10^{-7}-10^{-1} nM^{-1} s^{-1})

(Bistability range: 0.083-0.12 nM^{-1} s^{-1})

According to the Ozbabacan et al. association constants for transient protein protein interactions lie in the millimolar or micromolar range.
Ozbabacan et al. 2011[1]
k^{-}_{3} 60-6 \cdot 10^{4} [4] [5] min^{-1} 630 s^{-1}

(Range tested: 0-10^{3} s^{-1})

(Bistability range: 460-630 s^{-1})

According to Northrup et al. the K_{a} of protein-protein bond formations occur in the order of 10^{6} M^{-1}s^{-1}, this value is used to calculate the dissociation rate for the ScbR-ScbA binding. Therefore the range of the k^{-}_{3} values is calculated as per k^{-}_{3}=K_{d3} \cdot K_{a}.
Northrup et al. 1992[5]

Parameters with uncertainty

Since the values we are using for this parameter correspond to generic association constant values of a wide range of protein-protein interactions and not specifically to GBL or related systems, we wish to explore the whole range of values and investigate the conditions under which the ScbR-ScbA complex formation would be feasible. Therefore, we set the mode of the log-normal distribution for K_{d3} to  7 \cdot 10^{4} nM and the confidence interval factor to  10 . Thus, the range where 95% of the values are found is between  7 \cdot 10^{3} nM and  7 \cdot 10^{5} nM .

Similarly, the mode of the log-normal distribution for k^{-}_{3} is set to 2 \cdot 10^{4} min^{-1} and the confidence interval factor to 2.5. This means that the range where 95% of the values are found is between  8 \cdot 10^{3} nM and 5 \cdot 10^{4} min^{-1}.

The probability distributions for the two parameters, adjusted accordingly in order to reflect the above values, are the following:

500px 500px

The location and scale parameters of the distributions are:

Parameter μ σ
K_{d3} 11.9714 0.90284
k^{-}_{3} 10.0888 0.4305

References