December 24, 2007

Volume 85, Number 52

p. 10

Biochemistry

Antibodies Against RNA

Library method to generate antibodies is widely applicable

Carmen Drahl

FOR THE FIRST TIME, researchers have used a generally applicable method to elicit antibodies against RNA. This achievement promises to bring routine antibody technology from protein research to the burgeoning RNA field. It could lead to the widespread use of RNA-binding antibodies in RNA structure determination and biochemical and medical diagnostics.

Traditional immunization-based antibody technology is not used to elicit antibodies to RNA, because nucleases degrade RNA that's injected into an animal. The new anti-RNA antibodies come from an existing library of phage-displayed synthetic antibody fragments that a team led by three University of Chicago professors—chemist Joseph A. Piccirilli and molecular biologists Shohei Koide and Anthony A. Kossiakoff—screened for binding to RNA.

The screening identified two antibody fragments that bind tightly and specifically to the 3-D structure of a model RNA called ΔC209 P4-P6. The team used one of those fragments to assist crystallization of the model RNA, making it possible to resolve its X-ray crystal structure at higher resolution than was attained previously (Proc. Natl. Acad. Sci. USA, DOI: 10.1073/pnas.0709082105).

Proteins can help RNA crystallize because "a protein's surface is more amenable to forming crystal packing interactions than a nucleic acid's," says William G. Scott of the University of California, Santa Cruz, a crystallographer who specializes in RNA structure.

In the presence of the antibody fragment, the model RNA maintains its previously observed structure. The fragment forms a pocket around a protruding uridine nucleotide in the RNA. Such bulged nucleotides, which are common in RNA structures, could provide a generalized handle for antibody binding, according to Piccirilli.

The team has "developed a technology that has many promising applications, given the ubiquitous functions of RNA in the cell," says Adrian R. Ferré-D'Amaré of Fred Hutchinson Cancer Research Center, Seattle. Although the library that yielded the RNA antibodies was designed to unearth protein-binding antibody fragments, the team is now engineering libraries better suited to RNA. Adjustments to the library have yielded antibodies to other RNAs, Piccirilli says.

Antibodies to proteins or polysaccharides are invaluable in cellular imaging and disease detection. The team hopes its approach will facilitate exploration of RNA's roles in biology.

Chemical & Engineering News

ISSN 0009-2347

Copyright © 2008 American Chemical Society