Wakana received her B.S. in Agriculture at Hokkaido University, Japan in 2018. She began her research career as an undergraduate under Dr.Takasuka, studying biomass-degrading enzymes, and Dr. Kato, studying the discovery of bioactive natural compounds.
In 2018, Wakana started graduate school at the University of Minnesota, and joined Dr. Kate Adamala’s lab. She is interested in enzyme engineering for natural product synthesis and gene-based tool development for biocomputer.
The HTGAA course is based on the classic Fab-Lab “Hot to Make Almost Anything” fabrication class.
BioAcademy is the best resource to learn basisc of bioengineering, including specific applications of most cutting edge techniques. We run a synthetic cell module, including overwiew of the field of synthetic life and examples of synthetic cell based tools for biological engineering.
Excellent resource for beginning and advanced DIY biological engineers, biospaces and self-taught biohackers, as well as interesting supplement for anyone studying basics of modern biological engineering.
Build-a-Cell is an international community of scientists and policymakers working on building synthetic cells. We facilitate collaborations between groups in different areas of synthetic cell research, we engage with scientists in other disciplines to promote use of synthetic cell tools, and we provide information for the general public.
Our lab participated in every one of the bi-annual Build-a-Cell workshops, and we are actively pursuing collaborations with many Build-a-Cell members.
Kate Adamala is the co-founder and leader of Build-a-Cell.
The HTGAA course is based on the classic Fab-Lab “Hot to Make Almost Anything” fabrication class.
BioAcademy is the best resource to learn basisc of bioengineering, including specific applications of most cutting edge techniques. We run a synthetic cell module, including overwiew of the field of synthetic life and examples of synthetic cell based tools for biological engineering.
Excellent resource for beginning and advanced DIY biological engineers, biospaces and self-taught biohackers, as well as interesting supplement for anyone studying basics of modern biological engineering.
Astrobiology is studying past, present and future of the life on the Universe. Synthetic cells are the perfect tool to answer many of the questions typically asked by astrobiologists, including engineering synthetic cells to resemble earliest terrestrial life forms for studying of the origins of life on Earth, engineering synthetic cell systems to explore possibilities of biochemistries yielding life on other planets, and exploring possible future evolution scenarios for various life forms. Using synthetic cells we can ask many questions about “weird life” events and alternative life forms, questions that would be nearly impossible to answer studying modern, complex terrestrial cells.
Our work is driven by the question of what is the multidimensional niche space for life, and what are the molecular mechanisms of these boundary physicochemical conditions of life? This leads naturally to the questions of how does terrestrial life responds to changes at those boundary conditions, and can synthetic biology be used to expand these? We aim at defining comprehensive matrix describing mechanisms in which environment restricts basic processes of biology, and developing framework for studying and designing living systems around those limitations.
Exploring the Informational Transitions Bridging Inorganic Chemistry and Minimal Life
Understanding what separates life from non-life is critical to solving some of the great outstanding questions in science, such as how life first emerged and how we might unambiguously detect life on other worlds. The transition from non-living to living matter has been notoriously difficult to quantify, limiting our ability to develop the necessary theory for understanding life or its universal properties. One of the most significant challenges is the complexity of the examples of life available to study, which represent the product of more than 3.5 billion years of evolution. Systems representing the intermediate stages of complexity between simple chemistry and modern biology are only now becoming accessible to study in the lab with advances in systems chemistry and minimal synthetic life, respectively. These have not yet been connected to explore the uncharacterized landscape between simple chemical systems and the much more complex biochemical architectures characteristic of life today. Our project is an unprecedented opportunity to systematically study the full pathway from non-life to life through a synthesis of bottom-up chemistry, top-down minimal biology and fundamental theory. We aim to build very simple systems from chemical and biological parts, and by studying varying stages of programmed complexity and autonomy, systematically evaluate the transitions in information through which these become more life-like, self-referential entities.
We are developing solutions for automating and scaling thropought of synthetic cell epxeriments. Microfluidic rigs help us work faster, iterating more genetic circuit designs with automated liposome formation and streamlined detection of protein expression.
Our first rig recently started producing droplets with fluorescent RNA.
Most of the efforts of biological research, both in studying healthy organisms as well as disease states, is focused either on studying the whole live cell (or organism), or on studying isolated reactions between few purified and well defined components in vitro. Most biological processes are not isolated events of interaction between few components, but rather complex interconnected networks built of often multifunctional nodes (proteins acting on many targets). The in vitro studies give results that are less relevant to natural biology – since an experiment with a few purified components does not acknowledge the vast complexity of a natural system. On the other hand, live cell studies are notoriously hard to reproduce and interpret, due to the variability between live subjects, as well as due to the inherent complexity of biology (cross-talk between the studied process and other pathways, or background signal from unrelated processes is often present).
Synthetic minimal cells deliver a solution bridging the existing gap between in vitro and live cell research: use synthetic minimal cells to investigate multicomponent gene pathways, combining the advantages of in vitro systems with the relevancy and complexity approaching that of whole cell studies.
Reading and controlling cells is the core purpose of modern synthetic biology, and the overarching goal of all biomedical studies. Both studying mechanisms of most diseases, as well as investigating healthy cellular processes, is currently done as either in vitro or live cell experiments. In vitro research methods are easy to use, cheap and efficient way to obtain information about behavior of specific, well defined protein or nucleic acid complexes or single enzymes, or to characterize small molecule interactions between metabolites or drugs and their specific biological targets. However, since life is structured in complexes that involve many components organized in precise 3D assemblies, the in vitro experiments often only deliver information about small snapshot of this complex, natural system. Studies of live cells allow to obtain truly biologically relevant information about complex pathways, but at significantly higher cost, and with results that are harder to interpret and often less reproducible. The variability between live cell subjects and the underlying intricacy of interconnected biological networks constantly interacting with each other makes signal measured in live cell experiments often more noisy and the experiment itself difficult to design.
Synthetic minimal cells offer a platform that allows studying complex genetic pathways, while keeping the complexity of the system at a level that still allows us understanding fully what the system contains and how to engineer it. Our research focuses on building tools for general use in many areas of synthetic biology, as well as studying some specific cases of complex biological processes, both healthy and diseased, that are not accessible by studying natural complex cells.
During long term space missions, astronauts will encounter situations that are impossible to fully predict in advance. The isolation of the crew, for many years at a time, means that mission architecture needs to include plans for as many unpredictable situations as possible. The harsh environment of space and other planets will put high pressure on astronaut’s bodies. Providing on-demand, customizeable medical care under those conditions is very challenging.
We cannot plan for all pharmacy needs of astronauts by stocking the required drugs in advance. Long space missions require novel approach to producing pharmacticals on short notice from pre-defined, limited raw materials. Synthetic minimal cells provide just the right kind of programmable bioreactors that can be used to manufacture small molecule and biological drugs in short amount of time. Synthetic cells can be lyophilised and stored for a long time, and the programmability of the synthetic cell genetic circuits means almost every kind of chemical transition can be coded with the appropriate enzyme, and new enzymatic pathways for manufacturing drugs can be created on demand. Our research focuses on designing mission-oriented solutions for preparation and storage of synthetic cells for the purposes of small scale, fast and responsive manufacturing of pharmaceuticals.
Natural cells have a whole set of endogenous metabolic processes, pathways that use small molecules for suporrting the natural cell’s metabolism and growth. One of the biggest challenges in modern metabolis engineering is to integrate newly constructed pathways with the host metabolism. When trying to discover a new pathway, or improve efficiency of an existing enzyme pathway, we often run into the problem of not being able to tell whether the changes have the desired effect in the background noise of endogenous cell metabolism.
Synthetic minimal cells have no endogenous metabolism beyond what is engineered into those cells in the first place. Therefore, we can understand and control flux of small molecule substrates within the synthetic cell. This makes designing new pathways and optimizing existing ones much easier. Additionally, the short turnaround time of a synthetic cell experiment, without needing to wait for transformants to grow to test each new plasmid combination, make iterating metabolic engineering designs much faster.
Our research focuses on engineering methods for high throughput, combinatorial design of multi-gene pathways using synthetic cells as the chassis for testing and optimizing expression.
For large scale natural product synthesis, synthetic cells are mostly research and development tool, at this point it is still cheaper and easier to perform industrial scale production in a live bug. Synthetic cell screens can help identify candidate pathways, and optimize it before scaling up for industrial manufacturing.
Synthetic cell systems can be a good tool for small scale, pilot studies, or for rapid prototyping of on-demand production of small batches of biologicals or precious small molecule compounds.
Terrier Orion with synthetic cell experiment, launch at NASA Wallops, 2018 06 21
Synthetic cells can be used as a chassis for biological and biomedical experiments under the conditions of space flight: performing reliable RNA and protein production and formation of drug particles will be crucial for establishing human presence on the Moon, Mars colony and for maintaining the health of people and animals during space flights and colonization. They can be prepared in advance and stored, lyophilised, for a long time.
We have developed synthetic cell epxerimenta payload, with a team of the RockSat-C 18 program. The payload was succesfully launched in a Terrier Orion sounding rocket from NASA Wallops in June 2018, increasing the TRL of this project to 6. This was, to our knowledge, the first time cell-free protein expression experiment was performed under spaceflight conditions.
Synthetic minimal cells have been proposed as a possible tool for biomanufacturing during long-term space missions and on extraterrestrial colonies, as well as a tool for future terraforming efforts. Synthetic minimal cells are bioreactors built specifically to mimic certain aspects of cellular processes, by reconstituting specific genetic pathways, encapsulated within a biomimic membrane. Thus, synthetic minimal cell technology combines most advantages of classical in vitro studies, with added capabilities, including spatial interactions, and interactions between many scaffolded and encapsulated proteins at once.
Traditionally, the information contained in the genetic material can travel only as far and as fast as the mass of the nucleic acids being duplicated during cell division. In the case of synthetic cells, since their autonomous reproduction is unnecessary, once a winning formula for a particular synthetic cell is discovered locally, it can simply be transmitted as digital information riding on optical fibers or radio waves at high speed (and using digital compression makes high bit rates and practically zero error rates feasible with currently available apparatus). Such information can be reduced back to synthetic cells anywhere with a synthetic cell generating apparatus ‐ be it in another country, spaceship or planet.
Our work focuses on developing mission architecture: preparation, storage and experimental conditions compatible with various flight scenarios. We are building syntetic cells to model various natural processes, to study elements of biology under the conditions of spaceflight. The primary goal of this research is to gather information about how natural terrestrial organisms behave under space flight conditions, for the benefit of designing human space exploration strategies. The other goal of this research is to help refine physicochemical boundaries for biochemistry as we know it, to aid in designing life detection systems.
