About This Project
Zap-pore is a low-cost (10$), open-source DIY tool for electroporation, using everyday tools and common materials to transfer DNA into agrobacterium, an important model organism for plant genetic engineering and other microbes. DNA Transformation is a critical step in expressing proteins, and enzymes in microbes. Designed for resource-constrained settings, it nurtures creativity and hands-on learning in bacterial and plant synthetic biology.
Ask the Scientists
Join The DiscussionWhat is the context of this research?
We are in the midst of a biotechnology revolution, where living mechanisms are being studied and engineered at unprecedented rates. A fundamental technique in life sciences and synthetic biology is transformation: the insertion of foreign DNA, in the form of circular DNA strands (plasmids), into microbes (1). Transforming the microbe Agrobacterium tumefaciens is vital to genetically engineer plants (2). Furthermore, transformation is a critical step in expressing proteins, enzymes, and produce bio molecules of interest in microbes. Transformations are commonly conducted using an electroporator, where electric voltage is applied to generate pores in cell membranes, which enable uptake of DNA into the cell. Uptake of plasmids for a microbe is a function of voltage at which the pulse (Kilovolts) is applied, and duration of pulse (milliseconds) (3). However, the standard electroporators are expensive and they are out of reach for students and the under resourced.
What is the significance of this project?
In most educational settings, students use inefficient transformation methods, such as heat shock, because electroporation is too expensive (> 3000$). The consumables for electroporation are expensive ($3 per cuvette). The advantages of conventional electroporators are controllable voltage and usability. Disadvantages are high-cost, fixed pulse time, and high volume of biological reagents. Recent work demonstrated piezoelectric based electroporation ($0.20) after scaling up. The advantages are extreme low-cost. Disadvantages are fixed voltage, fixed pulse time, need for equipment such as 3D printers and need for high volumes of reagents. We propose Zap-pore, an open-source, low-cost (~ $10), DIY electroporator with control over voltages and pulse times and uses very low volumes of reagents. The tool enables scientific advancement in characterizing transformation properties of a wide variety of bacterial strains and allows users to genetically engineer plants using agrobacterium.
What are the goals of the project?
We developed Zap-pore, and we completed proof-of-concept experiments, demonstrating the tool’s usability. We developed a comprehensive user manual (will be published in an open access journal later). Currently, we are improving its efficiency and working on minimizing reagent consumption. Past hardware, we have to develop website where documentation is shared, along with ability for the user community to share results making and using Zap-pore.
Zap-pore will be implemented within MIT, targeting students. This focused approach will allow us to refine the tool and gather feedback. Once successful, we plan to expand its use, including incorporating it into the “How to Grow (Almost) Anything” course taught by Dr. Kong and Prof. Church with a new plant module (20 students at MIT, Harvard, and 100+ students who join virtually worldwide). We anticipate Zap-pore will benefit a diverse global audience, including universities, high schools, community biolabs, and maker spaces.
Budget
1. Procuring Materials and Prototyping:
○ Materials for beta testing and refinement of the tool: Gather all electronic components.
○ Prototyping: Continue refining the versions of the tool based on feedback and testing.
2. Undergraduate Training and Engagement: Organize workshops to train undergraduates on building and using Zap-pore.
○ Hands-on Support: Provide hands-on support and mentorship to help students build their own tools and conduct experiments.
3. Testing and Optimization:
○ Efficiency Testing: Measure efficiency and work on improving it. Implementation of the tool for agrobacterium and subsequent plant genetic engineering.
○ Reagent Minimization: Optimize the tool to reduce reagent consumption, crucial for resource-constrained settings.
○ User Testing: Conduct user testing of the final version with undergraduate students and the “How to Grow (Almost) Anything” course to gather real-world feedback and improve the tool.
Endorsed by
Project Timeline
The project timeline starts with procuring materials and prototyping in the first two months, followed by testing and optimization in months two to four. User testing and final adjustments occur in months five and six. The final phase, spanning months seven to twelve, focuses on the website launch and community outreach. Key steps include timely material procurement, thorough testing, responsive user feedback, and strategic outreach, all crucial for the project's success.
Dec 26, 2024
Project Launched
Jan 31, 2025
Procuring materials
Feb 28, 2025
Prototyping -Develop superior prototype
Apr 30, 2025
Testing and optimization - we will test for transformation efficiency for agrobacterium and improve while working on minimizing reagent consumption.
Jun 30, 2025
User Testing and Final Adjustments. Work with the MIT Biomaker space, targeting undergraduate students to refine the tool and gather feedback.
Meet the Team
Team Bio
Dr. David Kong has done pioneering work in developing automated fluidic tools and hardware for biological applications and applying open-source frameworks to biological hardware. He brings 10+ years of experience as a PI at MIT Media Lab and MIT Lincoln Laboratory in developing field tools which feature sample processing and multiple processes integrated within a single system. He also founded Metafluidics, an open repository of design files for fluidic systems.
Mani Sai Suryateja Jammalamadaka
Mani Sai Suryateja Jammalamadaka (Teja), a graduate researcher at MIT, has a background in mechanical engineering with a bachelors from BITS-Pilani and a masters in synthetic biology from CRI-Paris (Universite Paris Cite). He works on the interface of engineering and biotechnology for the development of low-cost biodevices and high throughput biological platforms. Before joining MIT, he carried out research work at MIT-Meche, Ecole Polytechnique and INSERM (France).
In addition to his research pursuits, he is actively engaged in teaching and mentoring. He has had the privilege of serving as a graduate teaching fellow and teaching assistant at MIT, where he has supported students in courses such as Quantitative and Evolutionary Biology, "How To Grow (Almost) Anything" and "How to Make (Almost) Anything" and Experiential Sustainability. He finds great fulfillment in sharing my knowledge and helping students from diverse backgrounds excel.
Furthermore, he is passionate about establishing collaborations and knowledge exchange in the scientific community. As a co-organizer of the Global Community Bio Summit, he curated workshops and facilitated networking among community bio labs worldwide.
Lab Notes
Nothing posted yet.
Additional Information
Zap-pore is not just about the technical achievement of reducing costs, but also about nurturing a deeper sense of ownership and intellectual curiosity among students and makers. By allowing students to build their own tools, we add a unique layer of knowledge and engagement that would be lost if the tools were simply provided as kits. This hands-on, playful approach is crucial for preserving the joy of making and exploring, which aligns perfectly with Experiment Foundation's values.
Project Backers
- 0Backers
- 0%Funded
- $0Total Donations
- $0Average Donation