Researchers have come up with a less expensive way to isolate and identify nanobodies that target various parts of the SARS-CoV-2 spike protein and are currently derived from llamas.
The findings, published in the Journal of Biological Chemistry, researchers describe a less expensive way to isolate and identify these so-called nanobodies, will make it easier for scientists around the world to try their hand at discovering nanobodies that target SARS-CoV-2 or other viruses.
“Our method is more straightforward and less expensive than existing techniques,” says Rockefeller University’s Michael P. Rout. “You do need a llama, but that - along with all the most complicated parts of the process - can be outsourced.”
The authors have already used this optimized method to identify multiple nanobodies that appear to work against key variants of the virus, including Omicron.
“COVID is clearly going to be a problem for some time,” Rout says. “We show that many of the nanobodies we have identified with this method target variants-of-concern, so they have real therapeutic potential.”
Compact size
Nanobodies may work where larger antibodies fail, in part due to their compact size. Studies have shown that nanobodies can squeeze into parts of the SARS-CoV-2 virus that larger antibodies cannot reach. Nanobodies also have unusually long shelf-lives, cost very little to mass produce and, because of their unique physical properties, could theoretically be inhaled.
Camelids such as llamas naturally produce nanobodies when exposed to a virus, and Rout and colleagues have developed enormous libraries of promising SARS-CoV-2 nanobodies by giving a small dose of COVID protein to llamas (which produce nanobodies in response, much as humans produce antibodies in response to a vaccine).
After taking small blood samples from the llamas and sequencing the nanobody DNA, the scientists later transfer key genes to bacteria which, in turn, produce many more nanobodies for lab analysis.
Time consuming libraries
But screening these nanobody libraries to see how well they work (and which variants they work against) can be time-consuming and expensive. Rout and colleagues have long relied on the “mass spectrometry” technique, which works extraordinarily well but requires substantial expertise to perform and expensive equipment.
They wondered whether a recently discovered “yeast display method”, which was potentially far less expensive and simpler, could also effectively sort through their nanobody library.
Rout, in collaboration with Rockefeller’s Fred Cross, started by first optimizing the yeast display method. They then used their optimized method to screen a library of nanobodies that they had previously screened with the mass spectrometry technique.
They found that their version of the yeast display method not only identified many of the same nanobody candidates as the other approach, but also identified numerous other candidates that they had missed.
“The method is not ours, but we made it simpler,” said Cross.
Low resource regions
The relatively simple and low-cost procedure described in the paper could empower laboratories in low-resource areas to generate nanobodies against SARS-CoV-2, as well as other viruses.
“A researcher anywhere in the world, with fairly limited resources, could use this technique,” Rout says. “The llama-related stuff could be FedEx-ed from North America.”
For COVID, the long-term goal is that techniques such as these will lower the bar for entry into nanobody research and ultimately produce therapies that prevent infection.
“How we’d make the therapeutic is unestablished, as yet,” Cross says. “The specificity is there and the activity is there, but we don’t have a drug yet. It’d be nice if we did. Hopefully someday.”
With COVID now transitioning to an endemic disease, novel methods for preventing the infection cannot come soon enough.
“New variants become prevalent by evading the immune system,” Cross says. “It’s important to have a fast way to find new nanobodies targeting the variants.”
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