Matthew Griffin, described as “The Adviser behind the Advisers” and a “Young Kurzweil,” is the founder and CEO of the World Futures Forum and the 311 Institute, a global Futures and Deep Futures consultancy working between the dates of 2020 to 2070, and is an award winning futurist, and author of “Codex of the Future” series. Regularly featured in the global media, including AP, BBC, Bloomberg, CNBC, Discovery, RT, Viacom, and WIRED, Matthew’s ability to identify, track, and explain the impacts of hundreds of revolutionary emerging technologies on global culture, industry and society, is unparalleled. Recognised for the past six years as one of the world’s foremost futurists, innovation and strategy experts Matthew is an international speaker who helps governments, investors, multi-nationals and regulators around the world envision, build and lead an inclusive, sustainable future. A rare talent Matthew’s recent work includes mentoring Lunar XPrize teams, re-envisioning global education and training with the G20, and helping the world’s largest organisations envision and ideate the future of their products and services, industries, and countries. Matthew's clients include three Prime Ministers and several governments, including the G7, Accenture, Aon, Bain & Co, BCG, Credit Suisse, Dell EMC, Dentons, Deloitte, E&Y, GEMS, Huawei, JPMorgan Chase, KPMG, Lego, McKinsey, PWC, Qualcomm, SAP, Samsung, Sopra Steria, T-Mobile, and many more.
WHY THIS MATTERS IN BRIEF
There are many parts of the world that need vaccines, especially in a pandemic, and this system will not only be fast it’ll be portable and be able to produce vaccines at scale.
Love the Exponential Future? Join our XPotential Community, future proof yourself with courses from XPotential University, read about exponential tech and trends, connect, watch a keynote, or browse my blog.
As the global COVID-19 pandemic hit the world faced many challenges but two were particularly urgent: first develop a vaccine then second make enough of it for everyone on the planet as quickly as possible. While organisations like DARPA were working on solutions to pandemics way before COVID-19 hit, such as their P3 program which aimed to identify pandemics and develop vaccines to stop them in their tracks in under 60 days, today we’re still seeing just how hard it is to manufacture viable vaccines at the speed and scale needed to get life back to the “new normal.”
Now GE have announced they’ve teamed up with DARPA on a moonshot project to create a revolutionary mobile vaccine platform that could fit on a truck and make potentially hundreds of millions of vaccines where they’re needed in days.
Standing in a lab on the GE Research campus in Niskayuna, New York, John Nelson holds up a sample of Synthetic DNA inside a vial that is small enough to fit comfortably between his thumb and forefinger. Nelson, who has worked as a senior principal scientist at GE Research for the last 24 years, says there’s enough synthetic DNA inside that half-gram vile to produce an estimated 5,000 vaccines.
“It took us under a day to produce this,” he says.
Now Nelson and his team are using their expertise in producing industrial amounts of synthetic DNA to take on a new challenge: finding a way to more easily and quickly mass-produce vaccines globally.
In August, GE Research and its partners were awarded an up to $41 million, five-year project by DARPA to help “develop a mobile medical manufacturing platform” that will be able to produce DNA and RNA-based vaccines in under three days.
This proposed production system is part of a new DARPA program managed by Dr. Amy Jenkins in the Biological Technologies Office called Nucleic Acids On-Demand Worldwide (NOW), and the program has two primary purposes: the first is to develop new technologies to improve the preparedness of deployed troops against bio-threat attacks, and the second is to tackle the threat of emerging infectious diseases.
As a dual use platform the system could be used by the military to more quickly distribute vaccines and therapeutics, such as some of the recently approved COVID-19 vaccines, as part of humanitarian operations.
“What our engineers like to say is that we’re taking an entire pharmaceutical processing plant and shrinking it down to fit within a 6-foot by 6-foot by 6-foot framework,” Nelson says.
Meet the GE Vaccine dream team
Of course, anyone who follows the news knows that producing enough vaccines for the entire population during a crisis and doing it quickly is a massive challenge. Mass production of DNA and RNA, the building blocks of many modern-day vaccines, typically takes weeks. The strands have to be assembled from oligonucleotides — short DNA molecules that have to be assembled into the DNA sequence, in much the same way that a puzzle is put together from a bunch of smaller pieces. Typically, the material needs to be grown in a lab using living cells before it is used to formulate a vaccine and injected into recipients’ arms.
Nelson, who holds 65 US patents, invented a synthetic method for making DNA in a shorter time and requiring less space and equipment.
“If you need a gallon of DNA to vaccinate Albany, that DNA is going to take multiple 500-liter fermenters of bacteria doing it the old way,” Nelson says. “What we’ve developed is a synthetic method to do that enzymatically using a much smaller container.”
They are using enzymes — proteins that catalyze biochemical reactions — to assemble the DNA and RNA. Unlike bacteria, Nelson and his team don’t need to feed the enzymes and clean up after them. Nelson says the process is like printing the same page of a cookbook and mass-producing a recipe.
“We’ve put the master copy in, we put all of our ingredients in, and we stick it in an incubator,” he says. “When we come back in roughly 10 hours, there are grams of pure DNA there, so we’ve eliminated fermenters growing bacteria and breaking that bacteria open to get the DNA from them.”
The project couldn’t be more timely amid the pandemic. The approach has the potential to be compatible with mRNA vaccines, which are the basis of COVID-19 jabs from Pfizer and Moderna. Those vaccines use messenger mRNA molecules to teach a person’s immune system how to make antibodies to keep a person from becoming sick if they come in contact with the virus.
Nelson along with his colleagues Weston Griffon, Erik Kvam and Brian Davis will oversee this DARPA research with a small, multidisciplinary team at GE Research known as RUN FAST (Rapid Universal Nucleic Acids using Fieldable Automated Synthesis Technology), some of whom have been working for two decades on a faster method for making larger quantities of DNA-based vaccine doses. By combining their expertise in chemistry, molecular biology and engineering with the talents of their partners at the Broad Institute, DNA Script, MedInstill, Molecular Assemblies and the University of Washington, the GE Research team believes it should be possible to integrate all of the steps needed to create a mobile vaccine production platform.
The final assembly, when it is ready, could fit inside a walk-in closet.
“Think of this generic box we’re making like a typewriter and a photocopy machine, but for vaccines,” he says. “We first print out the master version, then copy it over and over. Ultimately, what we will have to demonstrate with our box is that we have all the ink that we will need — we have all the tools within there for making these DNA copies — and that the copies that get made will have exactly the right sequence.”
Nelson has worked on many scientific and technological breakthroughs throughout his career at GE Research, including projects to amplify DNA from trace amounts in forensic samples, individual microbes and circulating tumor cells. With RUN FAST, he says he’s most excited about creating something for DARPA that could possibly go on to deliver tangible medical help to people on a large scale.
“I’ve done a lot of things that are considered novel, but this is a huge project that is trying to hook together a variety of really unique technologies in a completely automated way,” Nelson says. “It’s really exciting to know that we’re doing something that has never been done before; automating the production of pharmaceutical-grade DNA from scratch.”