Protein tail crucial to membrane fusion

RICE U. (US) — New findings shed light on the role that a protein plays in a group of hereditary neurological disorders that affects 20,000 people in the U.S.

The study, published in the journal Proceedings of the National Academy of Sciences, offers the first detailed account of the biochemical workings of atlastin, produced by one of the genes linked to hereditary spastic paraplegia.

The condition’s primary symptoms are progressive spasticity and weakness of the leg and hip muscles, resulting from the slow degeneration of the nerves that carry signals from the spinal column to the legs, feet, and toes.

While scientists know that HSP can result from more than two dozen different genetic mutations, they don’t know how the mutations cause nerve degeneration.

“We discovered a couple of years ago that atlastin plays a key role in building and maintaining an important internal compartment of healthy cells called the endoplasmic reticulum,” says James McNew, associate professor of biochemistry and cell biology at Rice University and the lead co-author of the study.

“HSP is known to primarily affect long nerve cells that can stretch from the lower back all the way to the base of the leg. It appears that atlastin plays a particularly crucial role in maintaining the health of these cells, and we want to know why.”

“Membrane fusion is a fundamental process involved in many cell functions, but only a few proteins can initiate it,” McNew says.

“Until 2009, we thought all membrane fusion proteins operated in the same basic way. Atlastin was completely different because it’s an enzyme that utilizes chemical energy to drive fusion. We really had to start from scratch to determine how it worked.”

Membranes are both the brick walls and the zip-lock bags of microbiology. Every living cell is encased in a water-tight membrane of fatty acids, and all of the cell’s interactions with the outside world are mediated by what can and cannot pass through that membrane.

When a virus invades a healthy cell, it uses membrane fusion. When a sperm fertilizes an egg, it uses membrane fusion. Membranes are also used inside the cell, where they serve as biochemical reaction chambers, as cargo containers and as pipelines.

To find out how atlastin initiates membrane fusion, researchers conducted  experiments involving the fruit-fly version of atlastin, which is remarkably similar to the version found in humans.

By selectively disabling portions of the protein and examining how those modifications affected atlastin’s ability to promote membrane fusion in the test tube and cell cultures, the team gradually built a picture of how atlastin works.

They found that pairs of atlastin proteins, each of which is anchored in a separate membrane, can bind to one another when both partners are functional enzymes. That action draws the separated membranes together and allows fusion to occur.

Additionally, they found that a small piece near the end of atlastin was required for fusion activity.

“Atlastin has a fairly short tail, which protrudes from the site where the protein is anchored into the membrane,” says Andrea Daga, a scientist at the Eugenio Medea Scientific Institute in Italy.

“When we deleted this tail, we found that the protein could not stimulate membrane fusion, even when the two copies bound together normally.”

Prior gene sequencing studies have show that some HSP patients have genetic mutations that result in defects in this critical tail region of the atlastin protein, McNew says.

“This study, as well as work by others, suggests the area of the cell where atlastin promotes membrane fusion, the endoplasmic reticulum, is a good target for future studies into the causes of HSP.”

The research was supported by the National Institutes of Health, the Mathers Charitable Foundation, the Italian Ministry of Health, the French Association Against Myopathies, and Telethon Italy.

The illustration shows how two atlastin proteins, each anchored in a separate membrane, bind to one another to initiate membrane fusion. The protein’s tail (light blue) plays a key role in initiating fusion. (Credit: J. McNew)

More news from Rice University: www.media.rice.edu/media/