Researchers discover protein’s ability to inhibit HIV release.
A family of proteins that promotes virus entry into cells also has the ability to block the release of HIV and other viruses, University of Missouri researchers have found. This is a surprising finding that provides new insights into the understanding of not only HIV infection, but also that of Ebola and other viruses. The study was published in the Proceedings of the National Academy of Sciences.
According to estimates from the Centers for Disease Control and Prevention, more than one million Americans currently are living with AIDS. AIDS, which stands for acquired immunodeficiency syndrome, is a condition characterized by progressive failure of the immune system. It is caused by the human immunodeficiency virus type 1 (HIV-1).
When HIV-1 or any virus infects a cell, it replicates and spreads to other cells. One type of cellular protein, T-cell immunoglobulin and mucin domain, or TIM-1, has previously been shown to promote entry of some highly pathogenic viruses into host cells. The researchers have found that the same protein possesses a unique ability to block the release of HIV-1 and Ebola virus.
This study shows that TIM proteins keep viral particles from being released by the infected cell and instead keep them tethered to the cell surface. This is true for several important enveloped viruses including HIV and Ebola. The medical community may be able to use this insight to slow the production of these viruses, the team state.
The researchers performed a series of experiments that revealed the protein’s ability to inhibit HIV-1 release, resulting in diminished viral production and replication.
HIV-1 attacks cells that are vital to the body’s immune system, such as T cells. These white blood cells play an important role in the body’s response to infection, but HIV-1 disrupts the cells’ ability to fight back against infection. When the virus enters a host cell, it infects the cell and replicates, producing viral particles that spread to and infect other cells. The researchers found that as the viral particles attempt to bud from, or leave, the infected cell, the TIM-family proteins located on the surface of the cell can attach to lipids on the surface of the viral particle.
These lipids, known as phosphatidylserine (PS), are normally present on the inner side of the cellular membrane but can be exposed to the outer side upon viral infection. When the TIM-family proteins come in contact with PS, the viral particle becomes attached to the host cell, keeping the particle from being released from the cell. Because TIM-family proteins and PS are present on the surface of the cell and the viral particle, the viral particles get stuck to one another, forming a network of viral particles that accumulate on the surface of the host cell, rather than being released to infect other cells.
By using molecular, biochemical and electron microscopic approaches, the researchers observed the TIM and PS interactions in human cells. The next step is for the researchers to study the biological significance of TIM-family proteins in animals and patients and to determine the fate of the infected cell once it accumulates a buildup of viral particles.
The team state that they are not yet at the point to draw a conclusion as to whether this is a positive or a negative factor. However, this discovery furthers the ultimate goal of understanding the biology of TIM-family proteins and potentially developing applications for future antivirus therapies.
Source: University of Missouri System
Michelle Petersen View All
I am an award-winning science journalist and health industry veteran who has taught and worked in the field.
Featured by numerous prestigious brands and publishers, I specialize in clinical trial innovation–-expertise I gained while working in multiple positions within the private sector, the NHS, and Oxford University, where I taught undergraduates the spectrum of biological sciences integrating physics for over four years.
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