Team:SDU-Denmark/project-m

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== Modeling ==
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== Physical Modelling ==
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'''Physical Modelling'''
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=== Motivation ===
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<p style="text-align: justify;">
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One of the main ideas in the project is to control the flow induced by a bacterial coating inside a micro-tube. What we want to do in this part of the project is to study the mechanics of such a system, and how different parameters will affect it. One way to do this is to create a physical model that describes the most essential features of the system. Our work connected to the development of such a model is presented in the following. The basis for any model is an understanding of the physical system in question, therefore we will start with a short review of the hydrodynamic properties of flagella and the bacterial pumping system constructed by M. J. Kim and K. S. Breuer [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 1]].
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</p>
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=== 1. Motivation ===
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=== The real system ===
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One of the main ideas in the project is to control the flow induced by a bacterial carpet in a micro-tube. This is done by changing the tumble frequency of the bacteria when they are exposed to light. It is however not clear what the exact connection between the tumble frequency and the overall liquid flow is. This matter is complicated by the fact that the bacterial pump it self is a selforganizing system and changing the tumbling of the bacterial could therefore change the structure of the overall system completely. One way to assess this connection between tumble frequency and the flow is to create a physical model, that describes the most essential features of the system. Our work connected to the development of such a model is presented in the following. The basis for any model is a understanding of the physical system in question, there will we start with a short review of the hydrodynamic properties of flagella and the bacterial pumping system constructed by[artikel reference].
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<p style="text-align: justify;">
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The "real" system that we want to model is a bacterial pump as described by M. J. Kim and K. S. Breuer  [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 1]]. In principle, this is just a microscopic chamber with a flow channel 15µm deep, 200µm wide and 15mm long, covered on the inside by a layer of flagellated bacteria. The bacterial layer described by M. J. Kim and K. S. Breuer [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 1]] is very dense and uniform, with a spacing between each bacterium of less that 1µm and 80% of the bacteria adhered to the surface as single bacteria. To get a better understanding of the origin of the  flow created from the bacterial coating, it is important to understand the structure of the bacterial flagellum.
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<br>
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The bacterial flagellum consists of 3 major parts, a rotary motor complex, a hook and a filament. The first part creates the rotary motion of the flagellum and the second part serves as a flexible coupling between the torque creating part and the filament. For our model the filament is the most interesting part. This is responsible for the conversion of the rotary motion into a linear thrust. The filament is a self-assembling polymeric structure composed of flagellin protein subunits. These are arranged in a circular way to create a hollow helical structure, with a typical width of 120-250Å and a length of 10-15µm [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 2]].<br> A bacterium like ''E. coli'' typically has around 10 flagella [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 3]]. These filaments are able to adopt a wide range of conformations under the induced torque. Numeric studies [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 4-5]] and empiric results [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 6]] suggest that the conformation is strongly dependent on the hydrodynamic environment that surrounds the flagellum and its rotational direction. When several flagella rotates counterclockwise, the flagella tend to bundle together in a single helix structure, due to the hydrodynamic interactions [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 4]]. A phosphorylation cascade causes the flagella to turn clockwise at irregular intervals. This induces a sequence of deformations that changes the single helix structure of the flagella and unravels the bundle. This is known as tumble mode. <br> </p>
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<br>
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[[Image:Team-SDU-Denmark-2010-The_real1.jpeg|thumb|center|550px|'''Figure 1''': Image '''A''' shows a shematic picture of the molecular structure of a flagellum [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 7]]. Images '''B''' and '''C''' show  the flagella of bacteria stuck to a surface and flagella bundles on a moving bacterium, respectively [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 6]].]]
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<br>
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<p style="text-align: justify;">To be able to model the flow created by a bacterial coating of a tube, it is essential to know what kind of flowfield a single flagellum/bundle will create. This has primarily been investigated by numerical approaches, where the flagella are modelled as semiflexible hookian systems. Several studies [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 4-5]] suggests that the flow created from a single flagellum is highly non-uniform, but to some degree circular symmetric at the end of the flagellum (see figure 2 A and B, below). When the flagella come together in a bundle, Floresa, H. ''et al.'' [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 4]] suggest that this symmetry becomes less clear and flow becomes even more complicated.
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</p> <br>
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[[Image:Team-SDU-Denmark-2010-The_real2.jpeg|thumb|center|550px|'''Figure 2''': Image '''A''' shows a cross section of a flowfield from a flagella modelled by Floresa, H. ''et al.''[[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 4]]. Image '''B''' shows the symmetry in the flagella flowfield depicted by Reicherta, M. ''et al.'' [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 5]].]]
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<br>
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<p style="text-align: justify;">All these results refer to flagella moving freely in aqueous solution, the question is now, whether the same is true for bacteria sticking to the surface of a narrow tube? Turner, L. ''et al.'' [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 6]] suggest that bacteria that are completely fixed to a surface will deviate from the bundle behavior, but it is unclear what happens if the fixation is only partial or if the bacteria are surrounded by a flow.
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<br>
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To summarize, we have to model a very dense system of elongated objects that each give rise to an unsymmetrical flow, which depends self-consistent of the total flow and gives rise to self-organization. This is indeed not a simple task, and quite a few simplifying assumptions will have to be made. These will be the starting point of the next part.
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</p>
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=== 2. The real system ===
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=== Description of model ===
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So the "real" system that we want to model is a bacterial pump as descriped by []. This is in principle just a small tube 15 $\mu m$ deep, 200 $\mu m$ wide and 15mm long, covered on the inside by a layer of flagellated bacteria. The bacterial layer described by [] is very dense and uniform, with a spacing between each bacterial of less that 1 $\mu m$ and 80$\%$ of the bacteria adhered to the surface as single bacteria. To get a better understanding of the origin of the created flow from this carpet, it is important to understand the structure of the bacterial flagellum.
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<p style="text-align: justify;">
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A flagellum creates propulsion by spinning around in a helical shape. Since the flagellum/flagellabundles take on a helical shape, the most accurate thing to do would be to model them as such, but doing this would become quite advanced for even one flagellum, not to mention an entire system. Since we are limited in both time and computer power, we will have to simplify the system a bit.
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<br>
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One thing we can do is to consider all the flagella of a bacterium to form one bundle, even though doing so for a bacterium stuck to a wall is questionable. <br>
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The overall result of this spinning bundle is that the flow moves in an almost straight line. This could be modelled as a pointforce on the tip of the flagellabundle pointing in the same direction as the bundle.
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The size of this force can be approximated by calculating the drag on a swimming bacterium. If the bacterium is considered almost spherical, the drag force can be calculated by using the formula for Stokes flow past a sphere:
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</p>
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[[Image:Team-SDU-Denmark-2010-Dragforce.gif|center]]
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<p style="text-align: justify;">
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where η (=8.94•10<sup>-4</sup> Pa•s for water) is the viscosity of the fluid in which the bacterium is swimming, r (=0.4•10<sup>-6</sup> m) is the radius of the bacterium and v (=50•10<sup>-6</sup> m/s) is the velocity of the swimming bacterium.
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</p>
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<p style="text-align: justify;">
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The dragforce and thereby the force created by the flagellabundle of one ''E. coli'' is
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</p>
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[[Image:Team-SDU-Denmark-2010-ColiForce.gif|center]]
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<p style="text-align: justify;">
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The system we are trying to model consists of a lot of bacteria stuck to a wall, but the part we are interested in is the flagella and the forces they create. We therefore ignore the bodies of the bacteria, and instead consider the flagella as being stuck directly to the wall, with one end glued to the wall and the other pointing out into the fluid.
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<br><br>
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Next step is to figure out what kind of flowfield such a pointforce creates. The flowfield created by a pointforce in a fluid with no walls or other obstructions near it can be calculated using the corresponding Green's function known as the stokeslet:
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</p>
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[[Image:Team-SDU-Denmark-Oseen 0.gif|center]]
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<p style="text-align: justify;">where the three indices on G represent the number of walls and their matrix-coordinates, h is the distance between the pointforce and the wall and r is the vector from the pointforce to where the flow is to be calculated.
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<br><br>
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If the pointforce is placed near a wall, modifications must be made since the flow velocity has to go to zero at the boundary (known as the no-slip condition). This is done by using the Oseen-Blake tensor. Simply described, the Oseen-Blake tensor creates a mirror image of our force on the other side of the wall, thus cancelling the flow near the wall (This is not a completely accurate description, but rather an intuitive one).<br>
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In our case the flagella are stuck to a wall, so we use the Oseen-Blake tensor.
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</p>
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[[Image:Team-SDU-student-Oseen 1 1.jpg|center]]
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<p style="text-align: justify;">
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Here R is the vector from the mirrorpoint of the force to the point where the flow is to be calculated.
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This consists of 3 major parts, a rotary motor complex, a hook and a filament. The first part creates the rotary motion of the flagellum and the second part serves as a flexible coupling between the touque creating part and the filament. For our pourpose is the filament the most interesting part. This is responsible for the conversion of the rotary motion into a linear thust. The filament is a self-assembling polymeric structure composed of flagellin protein subunits. These are arranged in a circular way to create a hollow helical structure, with a typical width of 120-250Å and a length of 10-15 $\mu m$. A bacteria as E. coli typically has around 10 flagella.[cyber cell] These filaments is able to adopt a wide range of conformation under the induced torque. Numeric studies[2] and empiric results [1] suggests that this conformation is strongly on the hydrodynamic environment that surrounds the flagellum and the direction of rotation. When several flagella rotates counterclockwise the flagella tends to bundle together in a single helix structure, due to the hydrodynamic interactions[2]. <<random biokemi!>> at some point causes the flagella to turn clockwise instead. This induces a sequence of deformations that changes flagella structure and unravels the bundle. This is know as tumble mode.  
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The two formulas above are based on [[https://2010.igem.org/Team:SDU-Denmark/project-m#Litterature 8]].
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To be able to model the flow created by a bacterial carpet it is essential to know what kind of flowfield a single flagellum/bundle will create. This has primary been investigated by nurmerical approatch, where the flagella is modeled as semiflexibel hookian systems. Several studies [][] suggests that the flow created from a single flagellum is highly non-uniform, but to some degree circular symmetric at the end of the flagellum.(see figure XX and XX) When the flagella bundle together [] suggest that this symmetry becomes less clear and flow becomes even more complicated. The total movement of the bacteria in tumble mode is zero, so to a first approximation can the field here be thought as non existing.  
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In our case the system we are trying to describe is a microtube. This means that the tube is so narrow that the forces created by the flagella are not only close to the wall to which the bacteria are stuck, but also close to the opposite wall. This presents an interesting problem. Since the Oseen-Blake tensor works by creating a mirrorpoint of the real force on the opposite side of the wall, we will need a mirrorpoint behind the other wall if we are to uphold the no-slip condition. But the mirror forces also affect the flow near the other wall. In order to cancel this effect one could create another mirrorforce, corresponding to each of the mirror forces, but of course these would obstruct each other to, requirering yet more mirror forces. In the end we decided to see how precise the system would be for one mirrorpoint behind each wall. This corresponds to taking the equation above and adding the three last terms once more, but with the mirrorvector corresponding to the other wall.<br>
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The flowfield corresponding to this is shown below.
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Now we can return to the All these results refers to flagella moving freely in aquas solution, but this is severly different from the heighly constrained microtube where the bacterial carpet is placed XX.
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</p>
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<br>
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[[Image:Team-SDU-Denamrk-Pointforces_notxt.jpg|thumb|center|580px|'''Figure 3''': All 3 images show the flowfield created by a pointforce at (0.000007,0.000007) with an angle of 45 degrees with the x-axis. In the first image there are no walls. In the 2nd a wall is placed at y=0. In the 3rd one wall is placed at y=0 and one at y=0.000015]]
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<p style="text-align: justify;"><br>
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As the above figures show, there is quite a difference depending on how many walls you take into consideration. We decided to keep working with both the single-wall and the double-wall flowfields.
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</p>
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To summarize we have to model a very dense system of . This is indee not a simple task, and quite a few simplification assumptions have to be made. These will be startingpoint of the next partXX
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=== Flagella dynamics ===
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<p style="text-align: justify;">
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The next thing to be considered was how the flagella depend on the fluid flow, i.e. if we place a bacterium at an angle θ with the wall, will it remain at that angle or will it get pulled around by the flow in the tube, thus changing its position? The two extreme situations would be either that the flagella stick very hard to the surface and are therefore unaffected by the flow or that they stick very gently to the surface and that their angle depends completely on the flow. In order to create an intermediate situation, we could constrain each flagellum with a harmonic potential, pulling it toward a favored angle (connected to the initial orientation of the fagella when it stick to the surface). We believe the answer lies somewhere in between the two extremes, but that does not mean the extremes can't tell us anything. We therefore decided to create a model in which the flagella keep still, and one where they are affected by the flow and a potential. The size of the potential can always be set to zero if we want to study the flagella without an affecting potential.
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<br><br>
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=== 3. General description ===
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The basic idea then is that every flagella stuck to the surface creates their own flowfields. To get the entire flowfield we add together all the flowfields created by the individual flagella. In the case where the flagella are stationary the assumptions made so far actually shows the system. For flagella that are able to move it's a bit more tricky.<br>
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A flagellum creates propulsion by spinning around in a helical shape. Many who models a single flagellum considers this shape rigid and then calculate a flowfield from the spinning helix. Our system consists of many flagella and modelling every single flagellum in this way would take too much time.
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An e. coli typically has around 8-10 flagella, but for simplicity we will consider them as one bundle.
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The overall result of the spinning flagellum/flagellabundle is that the bacterium moves in an almost straight line. We will therefore consider the forces created by the flagella to be simply a pointforce on the tip of the flagellabundle pointing in the same direction as the bundle.
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The size of this force can be approximated by calculating drag on a swimming bacteria. If the bacteria is considered almost spherical the drag force can be calculated by using the formula for stokes flow past a sphere:
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<math> F_d = -6 \pi \eta r v </math>
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where η is the viscosity of the fluid in which the bacterium is swimming, r is the radius of the bacterium and v is the velocity.
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Using the following data
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The first thing we had to figure out was how the flow created by all of the other flagella would affect one single flagellum. To do this we decided to approximate a flagellum as a string of spheres and use dragforce calculations to figure out the force with which the flowfields of the other flagella would affect the spheres. An image, showing some of the vectors involved and the procedure we used is shown below. <br>
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<math> r = 0.4*10^-6 m </math>
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[[Image:Team-SDU-Denmark-flagel.jpg|thumb|center|580px|'''Figure 4''': Sketch of the principial structure of the model.]]
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<math> v = 50*10^-6 m/s </math>
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<math> \eta = 8.94*10^-4 Pa*s </math>
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the dragforce and thereby the force created by the flagellabundle of one e. coli is
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<br>First, the fluid velocity at the given point is found. The method is the same whether there is 0, 1 or 2 walls, but the tensor used varies. <br>
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<math> F_d = 3.37*10^-13 N </math>
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</p>
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[[Image:Team-SDU-Denmark-Flow.gif|center]]
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The system we are trying to model consists of a lot of bacteria stuck to a wall, but the part we are interested in is really the flagella and the forces they create. So we ignore the bodies of the bacteria, and instead consider the flagella as being stuck directly to the wall, with one end glued to the wall and the other pointing out into the fluid.  
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<p style="text-align: justify;">The dragforce created by the fluid on the sphere is calculated using the same formula we used in part 3</p>
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[[Image:Team-SDU-Denmark-2010-Force-2.gif|center]] <br>
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Next step is to figure out what kind of flowfield, such a pointforce creates. The flowfield created by a pointforce in a fluid with no walls or other obstructions near it can be calculated using the corresponding Green's function known as the stokeslet. This gives the following flowfield:
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<p style="text-align: justify;">Once we have the force, we can use it to calculate the torque on the sphere, then we summarize the torques of the individual spheres to get the total torque </p> <br>
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[[Image:Indsæt billede af flowfield her]]  
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[[Image:Team-SDU-Denmark-2010-Torque-2.gif|center]]
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If the pointforce is placed near a wall modifications must be made, since the flowvelocity has to go to zero at the boundary (known as the no-slip condition). This is done by using the Oseen-Blake tensor. Simply described what the Oseen-Blake tensor does, is to create a mirror image of our force on the other side of the wall, thus cancelling the flow near the wall. (This is not a completely accurate description, but rather an intuitive one.)
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<p style="text-align: justify;"><br>We then transformed the torque to angular acceleration by dividing with the inertia. This is also where we introduce the potential, that we mentioned earlier</p>
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In our case the flagella are stuck to a wall, so we'll be using the Oseen-Blake tensor. A flowfield corresponding to this is shown below.
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indsæt flowfield
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[[Image:Team-SDU-Denmark-2010-Acceleration-2.gif|center]]
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In our case the system we are trying to describe is a microtube. This means that the width of the tube is so small, that the forces created by the flagella are not only close to the wall to which the flagella are stuck, but also close to the opposite wall. This presents an interesting problem. Since the Oseen-Blake tensor works by creating a mirrorpoint of the real force on the opposite side of the wall, we will need a mirrorpoint behind the other wall if we are to uphold the no-slip condition. But the mirror forces also affect the flow near the other wall. In order to cancel this effect one could create another mirrorforce, corresponding to each of the mirror forces, but of course these would obstruct each other to, requirering yet more mirror forces. In the end we decided, to see how precise the system would be for one mirrorpoint behind each wall. The flowfield corresponding to this is shown below.
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<p style="text-align: justify;">Now that we have the angular acceleration, we can insert it into the equation of motion. This allows us to calculate the position of the flagella at the next timestep by using its position at the current and at the previous timestep. </p> <br>
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Indsæt flowfield
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[[Image:Team-SDU-Denmark-2010-Angle-2.gif|center]]
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As the above figures show, there is quite a difference between the two situations. We decided to keep working with both the single-wall and the double-wall flowfields.
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<p style="text-align: justify;"><br>In the end, this model showed us that in less than 100ns the velocity of the flagella would be the same as the velocity of the fluid when the flagella started with a velocity of zero, after which the two velocities never diverged far from each other. Since the velocity of the flagella always went to the velocity of the fluid on such a short timescale and since these calculations took a lot of computer power we decided that instead of force calculations we would simpy find the flow velocity at the tip of the flagellum and convert that directly to the angular velocity of the flagellum.
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</p>
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The next thing to be considered was whether the flagella are dependent on the flow, ie. if we place a bacterium at an angle θ with the wall will it remain at that angle or will it get pulled around by the flow in the pipe, thus changing its position. The two extreme situations would be to either keep the flagella in a stationary position or to let it be completely dependent on the flow. In order to create an intermediate situation, we could induce each flagellum with a potential, pulling it toward a favored angle. We believe the answer lies somewhere in between the two extremes, but that doesn't mean the extremes can't tell us anything. We therefore decided to create a model in which the flagella keep still, and one where they are affected by the flow and a potential. The size of the potential can always be set to zero if we want to study the flagella without it.
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=== A 2-D model of the system ===
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<p style="text-align: justify;">
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In this chapter we will present our model a bit more precisely and present some of the results it has given us.
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The basic idea now is that every flagella stuck to surface creates its own flowfield. To get the entire flowfield we add together all the flowfields created by the individual flagellum. In the case where the flagella are stationary that is basically it. For flagella that are able to move it's a bit more tricky. This is described in the next chapter.
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The 2-D model consists of a one dimensional grid, to which flagella are attached. Each flagellum produces a force which creates a flow which pushes the other flagellum, and thus a dynamic system is created. To calculate how big the flow will be at a given point, a vector from the tip of the force-producing flagellum to the point where you wish to know the flow must be created. To know how a flagellum is affected by the flow, the flow at the tip of the flagellum must be calculated.  
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<br><br>
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Once you have this vector and the vector corresponding to the force, the flow can be calculated using stokeslet or the Oseen-Blake tensor, depending on whether there is a wall nearby. In our system there is a wall so we will be using the Oseen-Blake tensor. This means that we are also required to find a vector from the mirrorpoint of the force to the point at which we wish to know the flow.<br>
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=== 4. Considerations about velocity ===
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After this it is a matter of summarizing over all the flagella to find the total flowfield.
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The first thing we had to figure out was how the flow created by all of the other flagella would affect one single flagellum. To do this we decided to approximate a flagellum as a string of spheres and use dragforce calculations to figure out the force with which the flowfields of the other flagella would affect the beads.
 
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This model showed us that in less than 100ns the velocity of the flagella would be the same as the velocity of the fluid when the flagella started with a velocity of zero, after that the two velocity never diverged far from each other. Since the velocity of the flagella always went to the velocity of the fluid on such a short timescale and since these calculations took a lot of computerpower we decided that instead of force calculations we would simpy find the flowvelocity at the tip of the flagellum and convert that directly to the angular velocity of the flagellum.
 
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=== 5. A 2-D model of the system ===
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The situation (disregarding the mirrorpoint) is sketched in figure 4. The best way to illustrate the result from this model is to see it in action, so below the time series of a system of 20 flagella (only the 4 flagella in the middel of the system is shown), where the elastic constant is zero, is shown: </p>
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<html><center><object width="600" height="200"><param name="movie" value="http://www.youtube.com/v/XjkJIRt3IlI?fs=1&amp;hl=da_DK"></param><param name="allowFullScreen" value="true"></param><param name="allowscriptaccess" value="always"></param><embed src="http://www.youtube.com/v/XjkJIRt3IlI?fs=1&amp;hl=da_DK" type="application/x-shockwave-flash" allowscriptaccess="always" allowfullscreen="true" width="600" height="200"></embed></object></center></html>
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<p style="text-align: justify;">It is clear that the flagella tends to lie down and stabilize in an almost flat position in this case.
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In the following figure we have made many of these runs, but with varying average start-angle </p>
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First, we will make a model consisting of a 1D-grid, afterwards we will expand it to 2D.  
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[[Image:Team-SDU-Denmark--2010-start slut.jpeg|thumb|center|580px|'''Figure 5''': Shows the mean end angle as a function of the mean start angle, predicted by the 2D model.]]
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'''1D-model'''
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<p style="text-align: justify;">As the figure shows a very small deviation in the starting angle will cause a much bigger deviation in the end. The flagella in the systems used for making this graph were all lying down, but to which side the flagella went was highly dependent on the start configuration. When the mean angle was zero corresponding to a vertical flagellum it was pretty much 50-50, but when the start angles were pushed a bit to one side it had a tendency to shift the entire system in that direction. This tells us that if you can control the starting angle, it will go a long way towards creating a uniform flow.
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indsæt billede her
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</p>
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What we do from here is that we neglect the body of the bacteria. Instead we imagine that the flagella are glued to the surface off the pipe in such a way that they
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=== A stationary 2-D model ===
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<p style="text-align: justify;">
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The stationary model, does not offer much when it comes to dynamics and interesting behavior, which should not surprise anyone. It does however offer us the opportunity to investigate at which angle the flow in the tube is highest, which could be helpful when planning how to optimize the use of bacteria as a source of flow.</p>
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<math>\coprod_{i=1}^N x_i</math>
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[[Image:Team-SDU-Denmark-hastighed-vinkel-2.jpg|thumb|center|550px|'''Figure 6''': Shows the mean velocity in the z(perpendicular to the surface) and y(parallel to the surface) direction as a function of the flagella agle, pridicted by the static model.]]
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[https://2010.igem.org/Team:SDU-Denmark/Background#Literature 10]
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<p style="text-align: justify;">The above figure shows the average flow velocity as a function of the angle of the flagella. In the above case only one wall is taken into account. The one of most importance is the top-one which shows the flow velocity parallel to the tube. According to these figures we get the best velocity at an angle of around 0.7 rad or approximately 40 degrees, where the angle is measured from the axis perpendicular to the wall.
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</p>
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=== Model expansions ===
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=====3-D=====
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<p style="text-align: justify;">
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All the programs we have written have been created for easy transfer from the 2-D model to a 3-D model. We have made the adjustments needed in order for it to become 3-D, unfortunately we have not had time to check it for errors and to gain some results.
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</p>
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=====A flagella row on the other wall=====
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<p style="text-align: justify;">
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In our model we settled for placing bacteria on one wall. During the real-life application, flagella would most likely be placed on both walls. This is not something we have tried to implement in our model, although doing so should just be a matter of creating an extra grid and adapting the existing model to this. If this was done, it would improve the usability of the model.
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</p>
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===== A better double-wall approximation =====
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<p style="text-align: justify;">
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The double-wall approximation we made is a very rough approximation based on what you do when you have a single wall. The model could be improved a lot by making a better approximation, though aside from simply creating more mirror-points, we have not investigated how this could be done, but it would most likely be quite difficult.
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</p>
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=== References  ===
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<p style="text-align: justify;">
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[1] Kim M. J., Breuer K. S., [http://microfluidics.engin.brown.edu/Breuer_Papers/Journals/Small2008_Bacterial_Pump.pdf ''Microfluidic pump powered by self-organizing bacteria''], Small 4, 111-118. (2007)
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<br>
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[2] Berg H. C., [http://www.annualreviews.org/eprint/cDJrS190m62mDRwHrlp9/full/10.1146/annurev.biochem.72.121801.161737 ''The rotary motor of bacterial flagella''], Annu. Rev. Biochem. 72, 19-54. (2003)
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[3] Berg H. C., ''E. coli in Motion'', Springer, New York. (2004)
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[4] Floresa H., Lobatonb E., Méndez-Diezc S., Tlupovad S., Cortezd R., ''A study of bacterial flagellar bundling'', Bulletin of Mathematical Biology 67 137–168. (2005)
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[5] Reicherta M., Stark H., ''Synchronization of rotating helices by hydrodynamic interactions'', Eur. Phys. J. E 17, 493-500. (2005)
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[6] Turner L., Ryu W. S., Berg H.C., [http://jb.asm.org/cgi/content/full/182/10/2793?view=long&pmid=10781548 ''Real-Time Imaging of Fluorescent Flagellar Filaments''], JOURNAL OF BACTERIOLOGY, 2793–2801. (2000)
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[7] http://commons.wikimedia.org/wiki/File:Flagellum_base_diagram.svg
 +
<br>
 +
[8] Uchida N., Golestanian R., [http://prl.aps.org/abstract/PRL/v104/i17/e178103 ''Synchronization and Collective Dynamics in A Carpet of Microfluidic Rotors''], Phys. Rev. Lett. 104 178103 (2009)
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</p>
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=== 11. Litterature  ===
 
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1. hest hest
 
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We know what we expect from our system, but does the math agree?
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</p>
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Latest revision as of 20:34, 27 October 2010