# IGEM:IMPERIAL/2007/Dry Lab/Modelling/ID

(Difference between revisions)
 Revision as of 07:34, 20 October 2007 (view source) (→Formulation of the problem)← Previous diff Revision as of 07:41, 20 October 2007 (view source) (→Formulation of the problem)Next diff → Line 2: Line 2: ==Formulation of the problem== ==Formulation of the problem== - As described earlier, Infector Detector (ID) is a simple biological detector, which serves to expose bacterial biofilm. It functions by exploiting the inherent AHL production employed by the quorum-sensing bacteria, in the formation of such structures. + As described earlier, Infector Detector (ID) is a simple biological detector, which serves to expose bacterial biofilm. It functions by exploiting the inherent AHL production employed by the quorum-sensing bacteria, in the formation of such structures.
- Our project serves to improve on previous failures and relatively ineffective current methods of biofilm detection, first and foremost, by focussing on the sensitivity of the system, to low levels of AHL production (bacterial chatter).
+ Our project attempts to improve where previous methods of biofilm detection have proven ineffective: first and foremost, by focussing on the sensitivity of the system, to low levels of AHL production (bacterial chatter). - In doing so, a rigorous investigation of the level of sensitivity to [AHL] needs to be performed - in other words, what is the minimal [AHL] for appreciable expression of reporter protein. Furthermore, establish a functional range for AHL detection. How does increased [AHL] impact on maximal output of reporter protein?
+ In doing so, a complete investigation of the level of sensitivity to [AHL] needs to be performed - in other words, what is the minimal [AHL] for appreciable expression of reporter protein. Furthermore, establish a functional range for AHL detection. How does increased [AHL] impact on maximal output of reporter protein?
- Also, can the system performance be tailored, by exploiting the remaining state variables (e.g. varying initial [LuxR] and/or [pLux]). + Also, how can the system performance be tailored, by exploiting the remaining state variables (e.g. varying initial [LuxR] and/or [pLux]). - The system performance here revolves most importantly around AHL sensitivity; however, the effect on, maximal output of fluorescent reporter protein and/or response time is of much importance too. + + The system performance here revolves most importantly around AHL sensitivity; however, the effect on, maximal output of fluorescent reporter protein and/or response time is, likewise, of great importance. Our approach involves a proposal of two simple constructs, varying with respect to the manner in which LuxR is introduced into the system: Our approach involves a proposal of two simple constructs, varying with respect to the manner in which LuxR is introduced into the system:

# Model Development for Infector Detector

## Formulation of the problem

As described earlier, Infector Detector (ID) is a simple biological detector, which serves to expose bacterial biofilm. It functions by exploiting the inherent AHL production employed by the quorum-sensing bacteria, in the formation of such structures.
Our project attempts to improve where previous methods of biofilm detection have proven ineffective: first and foremost, by focussing on the sensitivity of the system, to low levels of AHL production (bacterial chatter). In doing so, a complete investigation of the level of sensitivity to [AHL] needs to be performed - in other words, what is the minimal [AHL] for appreciable expression of reporter protein. Furthermore, establish a functional range for AHL detection. How does increased [AHL] impact on maximal output of reporter protein?
Also, how can the system performance be tailored, by exploiting the remaining state variables (e.g. varying initial [LuxR] and/or [pLux]).

The system performance here revolves most importantly around AHL sensitivity; however, the effect on, maximal output of fluorescent reporter protein and/or response time is, likewise, of great importance.

Our approach involves a proposal of two simple constructs, varying with respect to the manner in which LuxR is introduced into the system:

• Construct 1 - represented by T9002, incorporates constitutive expression of LuxR by pTET.
• Construct 2 - simpler in nature, lacks pTET; LuxR is introduced in purified form here.

## Selection of model structure

• Present general type of model
1. is the level of description macro- or microscopic
2. choice of a deterministic or stochastic (!) approach
3. use of discrete or continuous variables
4. choice of steady-state, temporal, or spatio-temporal description
• determinants for system behaviour? - external influences, internal structure...
• assign system variables

#### Assumptions

• Ignore spatial information of the system; we ignore molecular dynamics of the system.
• Keep track of number of molecules of each type - concentrations of these state variables.
• Thus assume that the system is homogeneous - well-stirred, so that the molecules of each type are spread uniformly throughout spatial domain. *assume thermal equilibrium
• assume constant volume of spatial domain

## Our models

• Introduction

We can condition the system in various manners, but for the purposes of our project, Infector Detector, we will seek a formulation which is valid for both constructs considered.

Our initial approach assumed that energy would be in unlimited supply, and that our system would eventually reach steady-state (Model 1). Experimentation suggested otherwise; our system needed to be amended. This lead to the development of model 2, an energy-dependent network, where the dependence on energy assumed Hill-like dynamics:

### Model 1: Steady-state is attained; limitless energy supply (link here to derivation)

$\frac{d[LuxR]}{dt} = k_1 + k_3[A] - k2[LuxR][AHL]- \delta_{LuxR}[LuxR]$

$\frac{d[AHL]}{dt} = k_3[A] - k2[LuxR][AHL]- \delta_{AHL}[AHL]$

$\frac{d[A]}{dt} = -k_3[A] + k2[LuxR][AHL]- k_4[A][pLux] + k_5[AP]$

$\frac{d[P]}{dt} = -k_4[A][P] + k_5[P]$

$\frac{d[AP]}{dt} = k_4[A][pLux] - k_5[AP]$

$\frac{d[GFP]}{dt} = k_6[AP] - \delta_{GFP}[GFP]$

### Model 2: Equations developed through steady-state analysis; however due to limited energy supply, we operate in the transient regime

$\frac{d[LuxR]}{dt} = k_1\bigg(\frac{[E]^n}{K_E^n + [E]^n}\bigg) + k_3[A] - k_2[LuxR][AHL]- \delta_{LuxR}[LuxR]$
$\frac{d[AHL]}{dt} = k_3[A] - k_2[LuxR][AHL]- \delta_{AHL}[AHL]$

$\frac{d[A]}{dt} = -k_3[A] + k_2[LuxR][AHL]- k_4[A][P] + k_5[AP]$

$\frac{d[P]}{dt} = -k_4[A][P] + k_5[P]$

$\frac{d[AP]}{dt} = k_4[A][P] - k_5[AP]$

$\frac{d[GFP]}{dt} = k_6[AP]\bigg(\frac{[E]^n}{K_E^n + [E]^n}\bigg) - \delta_{GFP}[GFP]$

$\frac{d[E]}{dt} = -\alpha_{1}k_1\bigg(\frac{[E]^n}{K_E^n + [E]^n}\bigg) - \alpha_{2}k_6[AP]\bigg(\frac{[E]^n}{K_E^n + [E]^n}\bigg)$

where:

[A] represents the concentration of AHL-LuxR complex
[P] represents the concentration of pLux promoters
[AP] represents the concentration of A-Promoter complex
k1, k2, k3, k4, k5, k6 are the rate constants associated with the relevant forward and backward reactions
$\alpha_i \$ represents the energy consumption due to gene transcription. It is a function of gene length.
n is the positive co-operativity coefficient (Hill-coefficient)
$K_E \$ the half-saturation coefficient

The system of equations for the two constructs varies strictly with respect to the value of the parameter k1. Construct 1 possesses a non-zero k1 rate constant, whereas for construct 2, a zero value is assumed.