A collaborative crew from Penn Drugs and Penn Engineering has uncovered the mathematical rules behind a 500-million-year-old protein community that determines whether or not overseas supplies are acknowledged as buddy or foe.
How does your physique inform the distinction between pleasant guests, like drugs and medical gadgets, and dangerous invaders comparable to viruses and different infectious brokers? In accordance with Jacob Brenner, a physician-scientist on the College of Pennsylvania, the reply lies in a protein community that dates again over 500 million years, lengthy earlier than people and sea urchins developed alongside separate paths.
“The complement system is maybe the oldest-known a part of our extracellular immune system,” says Brenner. “It performs a vital position in figuring out overseas supplies like microbes, medical gadgets, or new medicine—notably the bigger ones like within the COVID vaccine.”
The complement system can act as each protector and aggressor, providing protection on one aspect whereas harming the physique on the opposite. In some circumstances, this historical community worsens circumstances like stroke by mistakenly focusing on the physique’s personal tissues. As Brenner explains, when blood vessels leak, complement proteins can attain mind tissue, prompting the immune system to assault wholesome cells and resulting in worse outcomes for sufferers.
Now, by way of a mix of laboratory experiments, coupled differential equations, and computer-based modeling and simulations, an interdisciplinary crew from the College of Engineering and Utilized Science and the Perelman College of Drugs has uncovered the mathematical rules behind how the complement community “decides” to launch an assault.
Of their examine revealed in Cell, the crew identifies a molecular tipping level referred to as the essential percolation threshold. This threshold is determined by how carefully complement-binding websites are spaced on the floor of the mannequin invader they designed. If the websites are too far aside, complement activation fades. If they’re shut sufficient—under the brink—it triggers a series response, quickly recruiting immune brokers in a response that spreads like wildfire.
“This discovery allows us to design therapeutics the way in which you’d design a automobile or a spaceship—utilizing the rules of physics to information how the immune system will reply—quite than counting on trial and error,” says Brenner, who’s co-senior creator of the examine.
Simplifying complexity
Whereas many researchers attempt to break complicated organic techniques down into smaller elements comparable to cells, organelles, and molecules, the crew took a distinct strategy. They considered the system by way of a mathematical lens, specializing in fundamental values like density, distance, and velocity.
“Not each side of biology will be described that manner,” says co-senior creator Ravi Radhakrishnan, bioengineering chair and professor in Penn Engineering. “The complement pathway is pretty ubiquitous throughout many species and has been preserved by way of a really lengthy evolutionary time, so we needed to explain the method utilizing a principle that’s common.”
First, a crew from Penn Drugs, led by supplies scientist Jacob Myerson and nanomedicine analysis affiliate Zhicheng Wang, exactly engineered liposomes—tiny, nanoscale fats particles typically used as a drug-delivery platform—by studding them with immune-system binding websites. They generated dozens of liposome batches, every with a exactly tuned density of binding websites, after which noticed how complement proteins sure and unfold in vitro.
The crew then analyzed the experimental information with mathematical instruments to evaluate the binding unfold dynamics and immune component recruitment charges and used computational instruments to visualise and simulate the reactions to determine when thresholds have been being approached.
What they noticed within the lab—that nearer spacing of proteins ramped up immune exercise—turned a lot clearer when considered by way of a mathematical lens.
The crew’s strategy drew from complexity science, a area that makes use of math and physics to check techniques with many transferring elements. By stripping away the organic specifics, they have been in a position to determine elementary patterns—like tipping factors and section adjustments—that designate how the immune system decides when to strike.
“We took that preliminary remark after which tried to manage exactly how carefully spaced proteins have been on the floor,” Myerson says. “We discovered that there’s this threshold spacing that’s actually the important thing to understanding how this complement mechanism can activate or off in response to floor construction.”
“If you happen to look solely on the molecular particulars, it’s simple to assume that each system is exclusive,” provides Radhakrishnan. “However while you mannequin complement mathematically, you see a sample emerge, not not like how forest fires unfold, or scorching water percolates by way of espresso grounds.”
The method of percolation
Whereas a lot of the analysis on percolation came about within the Nineteen Fifties, within the context of petroleum extraction, the physics matched these the researchers noticed in complement proteins. “Our system’s dynamics map fully onto the equations of percolation,” says Myerson.
Sahil Kulkarni, a doctoral pupil in Radhakrishnan’s lab, not solely discovered that the arithmetic of percolation predicted the experimental outcomes that Brenner and Myerson’s groups noticed, however that complement activation follows a discrete sequence of steps.
First, an “ignition occasion” happens, by which a overseas particle makes contact with the immune system. “It’s like an ember falling in a forest,” says Kulkarni. “If the bushes are spaced too far aside, the hearth doesn’t unfold. But when they’re shut collectively, the entire forest burns.”
Similar to some bushes in a forest fireplace solely get singed, percolation principle within the context of biology predicts that not all overseas particles have to be absolutely coated in complement proteins to set off an immune response. “Some particles are absolutely engulfed, whereas others get just some proteins,” Kulkarni explains.
It may appear suboptimal, however that patchiness is probably going a characteristic, not a bug—and one of many chief causes that evolution chosen percolation as the tactic for activating complement within the first place. It permits the immune system to reply effectively by coating solely “sufficient” overseas our bodies for recognition with out overexpending assets or indiscriminately attacking each particle.
Not like ice formation, which spreads predictably and irreversibly from a single rising crystal, percolation permits for extra diverse, versatile responses, even ones that may even be reversed. “As a result of the particles aren’t uniformly coated, the immune system can stroll it again,” provides Kulkarni.
It’s additionally power environment friendly. “Producing complement proteins is pricey,” says Radhakrishnan. “Percolation ensures you employ solely what you want.”
The following steps alongside the invention cascade
Wanting forward, the crew is happy to use their mathematical framework to different complicated organic networks such because the clotting cascade and antibody interactions, which depend on comparable interactions and dynamics.
“We’re notably fascinated with making use of these strategies to the coagulation cascade and antibody interactions,” says Brenner. “These techniques, like complement, contain dense networks of proteins making split-second choices, and we suspect they might comply with comparable mathematical guidelines.”
Moreover, their findings trace at a blueprint for designing safer nanomedicines, Kulkarni notes, explaining how formulation scientists can use this to fine-tune nanoparticles—adjusting protein spacing to keep away from triggering complement. This might assist scale back immune reactions in lipid-based vaccines, mRNA therapies, and CAR T remedies, the place complement activation poses ongoing challenges.
“These sorts of issues stay on the intersection of fields,” says Myerson. “You want science and engineering know-how to construct precision techniques, complexity science to cut back 100s of equations modeling every protein-protein interplay to a vital three, and medical professionals who can see the scientific relevance. Investing in crew science accelerated these outcomes.”
Reference: “A percolation section transition controls complement protein coating of surfaces” by Zhicheng Wang, Sahil Kulkarni, Jia Nong, Marco Zamora, Alireza Ebrahimimojarad, Elizabeth Hood, Tea Shuvaeva, Michael Zaleski, Damodar Gullipalli, Emily Wolfe, Carolann Espy, Evguenia Arguiri, Jichuan Wu, Yufei Wang, Oscar A. Marcos-Contreras, Wenchao Track, Vladimir R. Muzykantov, Jinglin Fu, Ravi Radhakrishnan, Jacob W. Myerson and Jacob S. Brenner, 13 June 2025, Cell.
DOI: 10.1016/j.cell.2025.05.026
Extra help got here from the Pennsylvania Division of Well being Analysis Method Fund (Award W911NF1910240), the Division of Protection (Grant W911NF2010107), and Nationwide Science Basis (Grant 2215917). Funding was additionally offered by the Chancellor’s Grant for Impartial Scholar Analysis at Rutgers College–Camden. Instrumentation was supported partly by the Abramson Most cancers Middle (NCI P30 016520) and Penn Cytomics and Cell Sorting Shared Useful resource Laboratory (RRID: SCR_022376.)