Anti-flu proteins work as designed, researchers confirm

Oct 02, 2012 by Lori Ann White
SSRL is aiding in the computational design of anti-flu proteins. Credit: Nikola Stojanovic/SSRL

(Phys.org)—Understanding why proteins interact with certain specific molecules and not with the myriad others in their environment is a major goal of molecular biology. Now, in a series of recent papers, researchers describe how they designed proteins from scratch to have a high affinity and high specificity for targets on flu viruses, and then validated the two best designs using X-ray diffraction data collected at the Stanford Synchrotron Radiation Lightsource (SSRL).

The validated proteins are now being developed as potential therapeutics against a wide range of health-threatening . If successful, this would mark the first example of proteins with therapeutic applications being designed using a computational model, rather than starting from observations of their natural activity in the laboratory – a processed termed de novo in biology and chemistry.

Nobel Prize-winning chemist Linus Pauling had suggested in the 1940s that a combination of many weak and nonspecific interactions, such as hydrogen bonding and , underlies the highly specific affinities between some molecules.

Following on that insight, a team led by David Baker of the University of Washington used massively parallel computing to virtually sift through numerous configurations of more than 800 natural proteins in search of a few configurations predicted to interact weakly with the target, a protein that enables flu viruses to attach to and invade cells lining the human respiratory tract.

A total of 88 of the computer-designed  proteins were produced in the lab, and further experiments isolated two of them that bound specifically to the target site. After additional optimization, the two proteins were shown to bind to the Spanish and versions of the flu with very high affinity. They also blocked the replication of H1N1 flu viruses in human cell cultures. What's more, studies at the SSRL showed that the structural details of the binding between these two designed proteins and Spanish flu protein were virtually indistinguishable from those designed in the computer, providing crucial atomic-level validation for the computational methods.

The team also made significant breakthroughs in understanding the design principles of natural functional sites while developing the computational methods they used to design their interactions.

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