Like a butterfly, immune protein 'flutters' in search of viruses

A hairpin loop from a pre-mRNA. Highlighted are the nucleobases (green) and the ribose-phosphate backbone (blue). Note that this is a single strand of RNA that folds back upon itself. Credit: Vossman/ Wikipedia

Researchers at Rutgers Robert Wood Johnson Medical School have identified an important step in the process that allows our bodies to fight viruses. Their work also explains how mutations that derail this process cause autoimmune disorders. This research, published Thursday in Molecular Cell, provides the framework to develop new treatments for viral infections.

For a to spread and cause an infection, it replicates itself inside of a host cell, the process of which generates viral nucleic acids such as DNA and RNA. However, our immune system has elaborate mechanisms in place to defend against both common viruses, such as influenza, and emerging viruses. The Rutgers team studied the process in which an immune receptor called RIG-I, which was discovered more than a decade ago to be a key player in the battle against RNA viruses, patrols the body in search of viral RNAs. Once the immune receptor discovers a viral RNA, it ends its search and activates the cell's antiviral response.

The study's author, Swapnil C. Devarkar, Ph.D., likened the process to a butterfly, "The continuous cycle of association and dissociation of RIG-I with RNAs is reminiscent of a butterfly. As a butterfly is constantly fluttering to and from anything that resembles a flower, similarly RIG-I is constantly sampling RNAs in the cell in search of a viral RNA." Dr. Devarkar is a post-doctoral fellow in the laboratory of Smita Patel, Ph.D., professor of biochemistry and molecular biology at the medical school.

When RIG-I discovers a viral RNA, not only does the fluttering stop, but it also signals for multiple molecules of RIG-I to gather on the viral RNA, activating the cell's antiviral response. The study has identified this as a critical step because it can only occur in the presence of viral RNAs.

In addition to this finding, the research team learned that RIG-I mutations previously linked with the autoimmune disorder Singleton-Merton syndrome cause defects in the that normally allows RIG-I to flutter away, or disassociate, from RNAs that do not contain viral signatures. When this occurs, according to the study, mutated versions of RIG-I become trapped in stable and long-lived complexes with cellular RNAs that eventually trigger abnormal immune responses.

According to Dr. Devarkar, given the importance of RIG-I in , autoimmune diseases, and cancer immunotherapy, the findings presented in this study can be used to leverage RIG-I in antiviral and cancer therapies.

Explore further

New technique reveals how Zika virus interacts inside our cells

More information: Swapnil C. Devarkar et al, RIG-I Uses an ATPase-Powered Translocation-Throttling Mechanism for Kinetic Proofreading of RNAs and Oligomerization, Molecular Cell (2018). DOI: 10.1016/j.molcel.2018.08.021
Journal information: Molecular Cell

Provided by Rutgers University
Citation: Like a butterfly, immune protein 'flutters' in search of viruses (2018, October 1) retrieved 2 April 2020 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Feedback to editors

User comments