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iGEM ETH Zurich 2014

Project Overview

Mosaicoli

Mosaicoli : from simplicity to complexity with biologic gates

Figure 1 A Textile Cone Snail ([http://en.wikipedia.org/wiki/Conus_textile Conus textile])
Location: Cod Hole, Great Barrier Reef, Australia
[http://commons.wikimedia.org/wiki/File:Textile_cone.JPG Photographer: Richard Ling (CC-BY-SA 3.0)]

What if these surprising patterns on sea snail shells would come from a simple rule, followed by all subsection on the shell?

For example in the picture below, you can see that a similar pattern can be produced by already a simple rule, in which every cell decides on its state (white or green) depending on the state of the 2 cells above it. This rule is called an XOR gate: If one of the two cells above is ON, the cell below them is ON, if both cells above are ON or if both cells above are OFF, the cell below is OFF.

As a matter of fact, many of the complex patterns you can see in nature come from simple rules. It is the case for hurricanes, flocks of birds, neural networks etc. We call this phenomenon emergence. Emergent phenomena are not predictable from the initial conditions and this is why they surprise us. If you are interested in emergence of complexity in general, you can read more about the background of our project.

As a team, we are driven by our fascination for the emergence of complexity and try to make these snail shells patterns, called Sierpinski triangles, emerge on our own grid of bacteria. To achieve this goal we encode the rule that leads to emergence of these patterns in the DNA of these bacteria. This approach, defined Synthetic Biology, is the application of engineering principles to the fundamental components of biology. Here we are using information processing principles in order to control the path of the information through all cells.

This way, Mosaicoli not only endeavors to learn more about how a complex pattern can emerge from simple rules, but also develops new tools for controlling communication between cells and implementing reliable biological circuits. For a more detailed description of our goals, go to the Goals section. For an outlook on the possible applications of our project, jump directly to Applications and outlook.

Background

"The whole is more than the sum of its parts" Aristotle

Emergence describes how novel properties can arise from lower-complexity parts, where these properties are not observed.^[12] This phenomenon is wide-spread in nature. One straight-forward example is water: from the molecules of H₂O, which are here considered as simple subparts, we are able to consider the liquid "water" at a higher level of complexity, with properties such as viscosity, pressure, transparency...

One particular pattern formation retained our attention: some sea snail present a complex pattern on their shells. The "Cloth of Gold" observed on textile cones results from an inner computation of the neural cells of the sea snail. This pattern appears row by row (computation after computation) and the pigments of the next row are determined by the pigments of the row before.

This pattern formation was formalized by Neuman in the concept of cellular automata. Following a simple pre-programmed logic rule, the state of a spot on the shell, corresponding to the color (either white or brown), is determined by the states of three parent spots (from the previous computation round). Wolfram ^[11] elaborated a whole theory on these cellular automata.

According to cellular automata theory, emergent patterns offer a large panel of properties: striking examples are the rule 30 which gives an apparently random pattern and the rule 110 which has been proven to be Turing complete. With cellular automata, you cannot predict how the final pattern will look like even if you know the rule that governs its property. Thus the intricated computations of steps poses the problem of complexity.

Our Project: Mosaicoli

Principle and goals

The aim of our project is to investigate the emergence of complexity and how we can deal with complexity in general. Our project addresses this goal in two ways.

First, we follow a biomimetic approach. This approach corresponds to the motto "What I cannot create, I cannot understand" (Richard Feynman). We are inspired by Sierpinski triangle patterns present on sea snail shells, and engineer the same kind of emergent patterns on grids of bacterial colonies. These patterns are emergent because they arise directly from one logic gate implemented in all bacteria. This project that combines modeling and wet-lab work will enable us to answer some questions such as how complexity can emerge from simple rules, whether it can be predicted from simple rules, how we can deal with crosstalk and leakiness of biological systems to enable a good predictability.

Second, we widen the scope of our investigation to other projects and disciplines, from scientific fields to philosophy, sociology or art. We address the issue of how to deal with complexity, by interviewing experts in several fields and conducting a larger scale study with a survey. Do these people consider that parts are strictly ordered, and try to reduce complexity to simple parts strictly following a set of deterministic rules, or do they accept that complexity comprises a mix of order and disorder, that a part of uncertainty cannot be neglected and that complex systems should be studied as a whole? Both approaches have their advantages and their drawbacks, which one should we choose to deal with the increasing complexity of our world?

Here is a more detailed list of subgoals:

Make a Sierpinski triangle pattern appear on a grid of bacteria
Conjugate quorum sensing and logic gates in bacterial colonies
Implement an XOR gate in an E. coli
Characterize integrases (retrieve missing parameters)
Lower the leakiness in quorum sensing systems
Study quorum sensing crosstalk in order to implement orthogonal communication
Be able to predict accurately the system’s behavior
Conduct a survey about how to deal with complexity
Gather interviews of experts from different fields
Find our own answer to this question thanks to our Mosaicoli

Implementation in E. Coli

More details

Mosaicoli involves three main plasmid constructs per cell, one for quorum sensing, one for production of integrases, and the last with the integrase-based XOR logic gate to perform computation. Each cell can receive two orthogonal N-acyl homoserine latones (AHLs) - the LuxI product N-(3-oxohexanoyl)-L-homoserine (3OC₆-HSL) and the LasI product N-(3-oxododecanoyl)-L-homoserine (3OC₁₂-HSL). The 3OC₆-HSL or the 3OC₁₂-HSL received by the cell bind to their corresponding receptor proteins LuxR and LasR, thus activating them. The LuxR-3OC₆-HSL or LasR-3OC₁₂-HSL complexes bind to the corresponding promoters Plux and Plas on the second plasmid and induce the expression of two integrases Bxb1 or ΦC31, respectively. Additionally, we use riboregulators to reduce leakiness in the expression of the integrase genes from the promoters P_lux or P_las^[10].

The integrases act on an asymmetric transcription terminator present present on the third plasmid, that contains the XOR gate. The terminator is located between a constitutive promoter and the start of two consecutive downstream genes in one operon, luxI and gfp. If the terminator is in its "functional” orientation, expression from these genes is not possible, because it is prematurely terminated. Further, the terminator is flanked by two pairs of opposing recombination sites recognised by ΦC31 and Bxb1, respectively. In the absence of both integrases, the terminator is in its functional orientation and thus blocks transcription. Expression of either integrase alone inverts the DNA encoding the terminator. It is no longer in its functional orientation and transcription of luxI (or lasI) and gfp is enabled. Presence of both integrases inverts the terminator twice bringing it back to its original functional orientation. Thus, transcription is blocked again^[9]. After the integrases acted on their corresponding recombination sites, the sites recombine in a way leaving the integrases unable to invert the region a second time.

Colonies of such cells are placed in a grid in a 3D-printed millifluidic chip. In each colony, all cells can exist in one of two states - ON or OFF. The cells are OFF if they do not produce any GFP and LuxI (or LasI) and ON when they produce GFP and LuxI (or LasI). The produced LuxI or LasI enzymes catalyse the production of the corresponding AHL molecules which diffuse out and are propagated to the colonies in the next row. Each colony updates its state by integrating signals from its neighbours (colonies in the previous rows). We expect to see complex fluorescent patterns, such as the Sierpinski triangles, after several rows of colonies on the grid have updated their states.

More details

E. coli bacteria are able to communicate by producing molecules that can cross their cell membrane by simple diffusion. These molecules are called quorum sensing molecules. In our project Mosaicoli, the cells in every colony on the grid are able to sense these molecules coming from the two colonies above it, and to produce a molecule for the next colonies below it.

In order to make a pattern appear on our grid, we need to tell every cell on this grid:

to sense the signals coming from the two cells above.
if it senses only one signal, to produce a fluorescent protein and generate the signal for the cells below
to produce nothing if it senses both signals or if it does not sense any signal.

In synthetic biology, you can tell the cell to compute this algorithm by inserting a genetic circuit. Here is how we did it:

For sensing the signals coming from above, we added in every cell two genes (luxR and lasR) that produce two proteins (LuxR and LasR) that will bind respectively the blue and the red quorum sensing molecules of the figure above. The blue and red complexes created this way trigger the production of other proteins called integrases (Bxb1 and ΦC31). Integrases flip a DNA sequence between two flanking sequences called att-sites (the triangles in the animation above).
This sequence between att-sites (see the large, black T in the animation above) is placed in such a way that it blocks production of a fluorescent protein. Once an integrase is present, the DNA sequence is flipped and production becomes possible. You can see in the animation that if an integrase is present, it can remove this blocking sequence (turn the black T upside down). However if both integrases are present, this sequence is flipped twice and it blocks production of fluorescence again.
When the fluorescent protein is produced, a second protein is produced as well which triggers the production of a quorum sensing molecule sent to the cells below.

If you want to know more about quorum sensing and integrases, you can read the article Biological tools in our Background page.

Biological tools: quorum sensing and integrases

Quorum Sensing

Bacteria, usually found in multi-species neighborhoods with billions of cells, where thought to live and divide isolated from its surroundings. However, bacteria do not try to out-compete the neighbors by mindless exponential growth but can exchange information via cell-to-cell communications in order to coordinate gene-expression and as a result the overall behavior of the population. This communicative endeavor is commonly described as quorum sensing and based on the synthesis, secretion and diffusion of small molecules or 'autoinducers'.

One of the best studied quorum sensing models was found in the Gram-negative bacterium V. fischeri in the early 1980s^[4]. Depending on the cell density and the corresponding autoinducer concentration, communication between the bacteria induces bioluminescence in the whole V. fischeri population. The small molecule responsible for this behavior was identified as N-(3-oxohexanoyl)-L-homoserine lactone, which is part of the N-acyl homoserine lactone (AHL) family. This AHL is synthesized by an enzyme called LuxI, diffuses through cell membranes and can then reach the cytosol of neighboring cells. There it binds to and activates LuxR, a protein positively regulating gene transcription. Subsequently to the investigation of V. fischeri, several other AHLs (with specific acyl side chains) and corresponding LuxR/LuxI like systems were found in various bacterial species, coordinating diverse responses including plasmid transfer, virulence, and antibiotic resistance^[5].

Here we focus in particular on the quorum sensing circuitry of V. fischeri and Pseudomonas aeruginosa, another Gram-negative bacteria. The additional systems are called LasR/LasI and RhlR/RhlI, also employing AHL molecules as autoinducers and are similar to the prototypical LuxR/LuxI system. Even though a key feature of quorum sensing molecules and its receptors is high specificity designed for intraspecies communication, the structural similarity of the different AHL molecules can cause unwanted gene expression. This cross-talk has to be taken into account when re-engineering LuxR/LuxI like systems for synthetic modules and circuits^[6].

Integrases

Site specific serine recombinases, or integrases, are enzymes recognizing pairs of short and non-identical DNA sequences. Within those sites they irreversibly catalyze the excision or unidirectional inversion of the DNA bases, depending on the orientation of the recognition sequence (often referred to as attB or attP). Many recombinases originate from phages integrating their genes into bacterial host genomes, hence they often do not require specific co-factors and are fully functional when heterologously expressed in bacteria. As a result, they can be employed as molecular tools in biotechnology^[7].

Due to the site-specificity, recombinases like Bxb1 and ΦC31 can be employed orthogonally in synthetic systems. In addition, the combination of multiple recombinases -and their corresponding specific recognition sites- with gene regulatory sequences like promoters and terminators, allowed the engineering of Boolean logic gates^[8]. For example, when an asymmetric terminator sequence is placed within a pair of recombination sites, the RNA polymerase can only proceed along this sequence if exactly one recombinase is available. Otherwise the terminator is blocking gene transription by default, or due to the repeated inversion, is again fully function as soon as both recombinases are present^[9]. Such recombinase-based logic gates are at the core of our genetic circuits.

Applications and outlook

Future development of synthetic biological systems will require the implementation of reliable synthetic circuits. These gene circuits will be designed to program new biological behaviour, dynamics, and logic control^[1]. A crucial part to coordinate and control the biological computation needed to perform their tasks can be seen in multichannel orthogonal communication. In order to achieve the goals of our project we need to thoroughly characterize available components, improve their performance, and develop novel constructs that get closer to actual multichannel orthogonal communication and subsequent logic processing. With our findings we will try to make a contribution to the field of biological computation by enabling further development of complex systems that rely on the interaction between its subparts.

These biological computers in turn also need to find a way to be implemented in patients, if they are developed to perform therapeutic tasks. A promising application of such synthetic biological systems is cell based therapy by alginate-microencapsulated implants^[2][3]. We will try to achieve communication and input integration in a grid of alginate beads and thus producing a more complex behavior than a single bead could show. This can be seen as a step towards the development of artificial organs composed of multiple alginate-microencapsulated implants, that work together to tackle tasks a single implant, which is not communicating with its neighbors, could not solve.

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Team:ETH Zurich/project/overview

From 2014.igem.org

Revision as of 12:12, 2 September 2014

Project Overview

Mosaicoli

Mosaicoli : from simplicity to complexity with biologic gates

Abstract

Mosaicoli : from simplicity to complexity with biologic gates

Background

"The whole is more than the sum of its parts" Aristotle

Our Project: Mosaicoli

Principle and goals

Implementation in E. Coli

More details

More details

Biological tools: quorum sensing and integrases

Quorum Sensing

Integrases

Applications and outlook

We thank our sponsors: