Antibody-biogel partnership can be stronger defense than previously thought, study proves

September 07, 2017

(Chapel Hill, N.C. -- Sept. 7, 2017) -- Strong molecular bonds between antibodies and biological gels, like mucus, aren't necessary to catch pathogens as was previously thought, according to new research from the University of North Carolina at Chapel Hill. In fact, rapid and weak interactions between antibodies and biogels are much better suited to locking down foreign invaders in the body's sticky first line of defense.

"Biological gels, like mucus, are abundant in the body and protect every opening and exposed organ not covered by the skin," said Sam Lai, an associate professor in the UNC Eshelman School of Pharmacy. "If we can trap pathogens in mucus and extracellular matrices, we can prevent them from getting to the cells they want to infect and, therefore, prevent infections from spreading or happening altogether."

Mucus and other biogels are networks of entangled polymer fibers. Conventional wisdom says that it is pointless to use antibodies to bolster the ability of these gels to trap bacteria, parasites, viruses and other invaders. The attraction between antibodies (proteins that bind to and flag pathogens in the body) and the polymer mesh is just too weak.

"Many people appreciate that antibodies have a high affinity for pathogens," said Greg Forest, the Grant Dahlstrom Distinguished Professor in the UNC Department of Mathematics and a longstanding collaborator of Lai's. "Antibodies also have an affinity for biological matrices, but the affinity is very weak, so few people paid attention to it. After all, why would weak and short-lived binding matter at all?

"Turns out it not only matters, it makes antibodies far more effective as a third-party booster of biogel barrier properties that can protect us from pathogens far better than the biogel alone."

In their previous work, Lai's group has shown that carefully engineered antibodies could bind pathogens and trap them in mucus in the lab. However, most scientists still believe a strong attraction between antibodies and biogels, just like strong attraction between antibodies to pathogens, to be essential for a strong defense. The UNC researchers explain that weak binding is actually better in an article published in Nature Communications.

"The paradox is caused by the fact that strong attraction between antibodies and the polymer mesh of biogels would actually compromise the ability for antibodies to bind pathogens" said Jay Newby, a postdoctoral fellow in the UNC mathematics department and co-first author of the study.

"Weak antibody-matrix interactions allow antibodies to quickly accumulate on the pathogen surface, where the collective antibody-pathogen complex could then become trapped in the polymer mesh."

It's like looking for a parking spot in a crowded lot, Lai said.

"If all the cars park for hours on average, then it is going to be very difficult for a new vehicle to find a spot. That's strong binding," he said. "But if each car is only parked for a minute or less, then you'll have no trouble finding a spot. That is how weak binding works. Rapid and weak interactions mean the antibody-pathogen complex has a greater chance to get stuck -- or 'park' -- before it can make its way through the mucus layer."

Jennifer Schiller, a graduate student in the Lai Lab and co-first author of the study, said providing the body with the proper antibodies is the key.

"You can think of antibodies as messenger molecules that help the body recognize what is foreign," Schiller said. "They're a critical part of the body's immune response."

Antibodies are proteins that recognize and bind to invaders, making it easier for the body's immune system to deal with them. The right antibodies can bind with a pathogen and then also bind with a biogel like mucus, effectively trapping the pathogen until it is removed by the body's systems.

"That's the game: immobilize the pathogen long enough for the barrier that it's caught in to be cleared naturally," said Schiller.

This work advances our understanding of basic immunology and demonstrates that the appropriate antibodies could prevent the spread of infections that are already present in the body by trapping them in mucus and other biological matrices, Lai said. This work will allow scientists to engineer better antibodies to trap a variety of pathogens, even sperm, for prophylactic and therapeutic applications.

Lai's work has spun off a company, Mucommune, which is working to engineer antibodies that can be applied topically to prevent diseases at the infection site. Currently all antibodies used to treat patients are given systemically to treat conditions such as autoimmune disorders and cancers. One example of an antibody drug that works systemically is Humira, which is used to treat rheumatoid arthritis and other conditions.

Topical antibodies would protect a specific infection site, Lai said. Swallowing a pill could protect the gut; a puff from an inhaler would protect the lungs.

"Nurses and doctors could get a daily nasal spray containing antibodies against a diverse array of flu strains," Lai said.
About the University of North Carolina at Chapel Hill

The University of North Carolina at Chapel Hill, the nation's first public university, is a global higher education leader known for innovative teaching, research and public service. A member of the prestigious Association of American Universities, Carolina regularly ranks as the best value for academic quality in U.S. public higher education. Now in its third century, the University offers 77 bachelor's, 111 master's, 65 doctorate and seven professional degree programs through 14 schools and the College of Arts and Sciences. Every day, faculty, staff and students shape their teaching, research and public service to meet North Carolina's most pressing needs in every region and all 100 counties. Carolina's more than 322,000 alumni live in all 50 states, the District of Columbia and 165 countries. More than 175,000 live in North Carolina.  

School of Pharmacy contact: David Etchison, (919) 966-7744,

University of North Carolina at Chapel Hill

Related Antibodies Articles from Brightsurf:

Scientist develops new way to test for COVID-19 antibodies
New research details how a cell-free test rapidly detects COVID-19 neutralizing antibodies and could aid in vaccine testing and drug discovery efforts.

Mussels connect antibodies to treat cancer
POSTECH research team develops innovative local anticancer immunotherapy technology using mussel protein.

For an effective COVID vaccine, look beyond antibodies to T-cells
Most vaccine developers are aiming solely for a robust antibody response against the SARS-CoV-2 virus, despite evidence that antibodies are not the body's primary protective response to infection by coronaviruses, says Marc Hellerstein of UC Berkeley.

Children can have COVID-19 antibodies and virus in their system simultaneously
With many questions remaining around how children spread COVID-19, Children's National Hospital researchers set out to improve the understanding of how long it takes pediatric patients with the virus to clear it from their systems, and at what point they start to make antibodies that work against the coronavirus.

The behavior of therapeutic antibodies in immunotherapy
Since the late 1990s, immunotherapy has been the frontline treatment against lymphomas where synthetic antibodies are used to stop the proliferation of cancerous white blood cells.

Re-engineering antibodies for COVID-19
Catholic University of America researcher uses 'in silico' analysis to fast-track passive immunity

Seroprevalence of antibodies to SARS-CoV-2 in 10 US sites
This study estimates how common SARS-CoV-2 antibodies are in convenience samples from 10 geographic sites in the United States.

Neutralizing antibodies in the battle against COVID-19
An important line of defense against SARS-CoV-2 is the formation of neutralizing antibodies.

Three new studies identify neutralizing antibodies against SARS-CoV-2
A trio of papers describes several newly discovered human antibodies that target the SARS-CoV-2 virus, isolated from survivors of SARS-CoV-2 and SARS-CoV infection.

More effective human antibodies possible with chicken cells
Antibodies for potential use as medicines can be made rapidly in chicken cells grown in laboratories.

Read More: Antibodies News and Antibodies Current Events is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to