Recently, a grassroots effort initiated by families and clinicians led to the discovery of a human genetic disorder with severe consequences that is linked to a mutation in the human NGLY1 gene. In a big step towards understanding the effects of this mutation, research by scientists at the RIKEN-Max Planck Joint Research Center implicate the enzyme ENGase as the factor responsible for deficient protein degradation that occurs in the absence of mouse Ngly1 gene expression. The study found that a lack of the Ngly1 peptide results in the incomplete removal of the sugar portion of glycoproteins, a process called deglycosylation. The result is that proteins that should be broken down in the cytostol are instead aggregated in the cells.
The ability of proteins to function and interact with other molecules properly often depends on their three-dimensional configuration, which can be changed through the addition or subtraction of sugar chains. When proteins are not made correctly, they are sent to be broken down in the cytostol. NGLY1 is a cytostolic enzyme that removes the sugar chains from specific types of glycoproteins, and ENGase is another cytostolic enzyme in animal cells that degrades the free sugars left behind. The big question is whether NGLY1 deficiency affects protein degradation, and if so, how.
The researchers tackled this problem by first creating a model glycoprotein for examining this process in animal cells. Next, they expressed the model protein in cells derived from four types of mice, wild-type, Ngly1 knockout, Engase knockout, and double knockout, and measured how much of the model protein was degraded and how much of the undegraded portion still had attached sugar chains.
As expected, they found sugar chains were not removed from the model protein in the double knockout cells because they lacked both of the deglycolyslation enzymes. Interestingly, Ngly1 knockout cells contained a normal proportion of de-sugared model protein. This indicated that ENGase might be responsible for the deglycosylation that occurred in the Ngly1 knockout cells.
Next, they inhibited protein synthesis in these four types of cells and found that normal protein degradation, both sugared and de-sugared, proceeded in the wild-type, Engase knockout, and double knockout cells. Critically, the amount of de-sugared protein remained high and undegraded in the Ngly1 knockout cells.
This indicated two key points. First, removal of sugar chains by ENGase appeared to have created a form of the protein that, in the absence of Ngly1 could not be degraded properly. To confirm this hypothesis, they used mass spectrometry and showed that when the model protein was de-sugared by ENGase, one sugar molecule remained attached to the protein. Second, normal protein degradation in the double knockout indicates that deglycosylation of the model protein by Ngly1 was not necessary as long as the incomplete removal of sugars by ENGase was prevented.
People with the NGLY1 mutation have many severe symptoms, from delayed development and epilepsy to abnormal liver function and the inability to make tears.
The team note that while it is currently unclear how these symptoms correlate with reduced protein degradation caused by insoluble aggregates, if the abnormal aggregation of this type of glycoprotein is somehow related to them, it is tempting to speculate that inhibition of ENGase activity may serve as a therapeutic target for patients carrying mutations in the NGLY1 gene.
Michelle Petersen is the founder of Healthinnovations, having worked in the health and science industry for over 21 years, which includes tenure within the NHS and Oxford University. Healthinnovations is a publication that has reported on, influenced, and researched current and future innovations in health for the past decade.
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An avid campaigner in the fight against child sex abuse and trafficking, Michelle is a passionate humanist striving for a better quality of life for all humans by helping to provide traction for new technologies and techniques within healthcare.