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Pando Bioscience screens ~1,000x more enzyme variants than traditional methods 75% faster, 80% cheaper: the pitch behind the one-pot screen Design-build-test-learn cycle compressed to about one month Founders are Ginkgo Bioworks and Harvard Medical School alumni Selected for Y Combinator Winter 2023 batch Proprietary polymerase Saiyan-Phi29 in the pipeline Pando Bioscience screens ~1,000x more enzyme variants than traditional methods 75% faster, 80% cheaper: the pitch behind the one-pot screen Design-build-test-learn cycle compressed to about one month Founders are Ginkgo Bioworks and Harvard Medical School alumni Selected for Y Combinator Winter 2023 batch Proprietary polymerase Saiyan-Phi29 in the pipeline
Biotech · Synthetic Biology · YC W23

The Company Teaching AI to Design a Better Enzyme

Pando Bioscience built a screening machine that tests roughly a thousand times more enzyme variants than a normal lab. Then it pointed a generative-AI model at all that data. The goal is unglamorous and specific: cheaper enzymes for the people who make medicine.

Enzymes are the quiet machinery of modern medicine. They stitch together drug molecules, copy DNA in diagnostic tests, and cut costs in factories most people never think about. When an enzyme is a little too slow, or a little too fragile, or works only under expensive conditions, the bill lands somewhere - usually in the price of the finished product. Pando Bioscience, a Watertown, Massachusetts company that went through Y Combinator's Winter 2023 batch, is built around the belief that most of those enzymes are quietly leaving money on the table.

The company's answer combines two things that biotech often keeps in separate rooms: a generative-AI model that proposes new enzyme designs, and a physical screening platform that tests them at high volume. The AI suggests specific mutations meant to improve several properties at once. The screen checks whether those guesses actually work. What comes back feeds the model again.

"Unlocking the full potential of enzymes to drive down costs and boost productivity in pharma."
The Bottleneck

The problem is throughput, not imagination

Designing an enzyme has never been the hard part. Testing enough of them is. Traditional directed evolution and screening are slow and expensive, which means an AI model trying to learn enzyme behavior is usually starved for data. Pando's central bet is that if you dramatically raise how many variants you can test, the AI finally has enough to learn from - and each cycle makes the next one smarter.

Pando says its ultra-high-throughput "one-pot" screening platform tests roughly 1,000 times more enzyme variants than conventional approaches, about 75% faster and 80% cheaper. The platform's trick is converting many different biological signals into abundant, quantifiable data across varied conditions - the kind of clean numbers a model can actually use.

1,000×More variants screened
75%Faster than traditional
80%Cheaper to run
Figure 1 — The design-build-test-learn loop, compressed to ~1 month
DesignAI proposes mutations
BuildVariants synthesized
TestOne-pot screen
LearnData retrains model
Round and round. Each faster loop is another lesson the model keeps. Speed here is not vanity - it is how the AI gets better.
Head to head

Why the screen is the moat

Plenty of startups claim "AI for proteins." Fewer talk about the boring machine that feeds the AI. Pando's differentiation sits in that unfashionable place - the screening throughput - because it is what turns a clever model into one that keeps improving. The chart below sketches the company's own framing of that gap.

Figure 2 — Variants tested per cycle (relative, company framing)
Traditional
~1x
Pando one-pot
~1,000x
Not to scale, by necessity. A true 1,000:1 bar would run off the page - which is roughly the point Pando is making.
The dirty secret of "AI for biology" is that most models starve for data. Pando's answer is to feed them.
What it sells

Two ways to make money

Pando works both sides of the enzyme market. For pharmaceutical, diagnostic, and biotech customers, it improves existing enzymes or discovers new ones - a services and engineering relationship aimed at cutting manufacturing costs and raising productivity. At the same time, it develops its own proprietary enzyme assets. One named example is Saiyan-Phi29, a high-fidelity Phi29 polymerase of the sort used in DNA amplification and sequencing.

That dual model - engineer for clients, and build a catalog you own - is a common shape in the enzyme business, and it hedges a young company between near-term revenue and longer-term product value.

Pando at a glance

  • What: AI-designed enzymes for pharma manufacturing and diagnostics
  • How: Generative-AI design + ultra-high-throughput one-pot screening
  • Cycle: Design-build-test-learn in about one month
  • Own product: Saiyan-Phi29 high-fidelity polymerase
  • Backing: Y Combinator, Winter 2023 (W23)
  • Base: 134 Coolidge Ave, Watertown, Massachusetts
The people

From a synthetic-biology unicorn to a five-person team

Pando was founded in 2022 by Will (Yangxiaolu) Cao and Yang Wang, who met the field the hard way. Cao, the CEO, was an early employee at Ginkgo Bioworks and, during her PhD, switched from engineering machines to engineering bacteria. She has published first-author papers in Cell and Nature Biotechnology. Wang spent six years at Harvard Medical School before also joining Ginkgo. Their shorthand for the company's focus is blunt: AI-guided enzyme engineering is in their wheelhouse.

Will Cao changed her PhD from engineering machines to engineering bacteria. That pivot is the whole company: stop building the machine, build the thing that builds it.

There is a small tell in the name, too. Pando is one of the largest and oldest living organisms on Earth - a single clonal aspen grove in Utah whose thousands of trunks share one root system. A company obsessed with iterating on biology at scale could not have picked a more on-the-nose namesake.

The map

Where Pando fits

The enzyme and protein-engineering space is crowded with capable names - established players and a wave of AI-first startups all promising better proteins. Pando's position is narrow on purpose. It is not trying to be a drug company or a platform for everything. It is trying to be the group that can iterate on an enzyme faster and cheaper than the customer could in-house, and prove it with data from its own screen. In a hype cycle full of "AI will cure everything," that narrowness reads less like a limitation and more like a plan.

Figure 3 — The market position, in one line
Slow, in-house enzyme R&D  →  Pando's AI + screen  →  Cheaper, higher-performing enzymes
The through-line. Everything Pando builds points at the same outcome: fewer wasted cycles between an idea for an enzyme and one that works.

For a customer, the pitch is concrete. Bring an enzyme that is holding back a process - too costly, too slow, too finicky - and Pando's loop tries to hand back a version that behaves. For the industry, the more interesting question is whether the screening-first approach compounds the way the company believes it will. Every faster loop is a wager that it does.

synthetic biology enzyme engineering generative ai protein design biocatalysis ultra-high-throughput screening pharma manufacturing molecular diagnostics yc w23