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Understanding Cell Surface Proteins’ Behaviour May Help Us Design Better, Less Toxic Drugs

A Simon Fraser University chemist is the lead author on a new paper that advances scientific of the structure and function of glycoproteins, in particular the number and positioning of sugars on them.

PLOS ONE, an international, peer-reviewed, open-access, online, , has just published the paper, N-glycoproteome of E14.Tg2a Mouse Embryonic Stem Cells.*

Glycoproteins are membrane proteins and are often involved in human diseases. They facilitate between cells, and interactions with pathogens, such as viruses and bacteria, and with external environments.

SFU chemist and her colleagues have discovered how nature can vary the amount of a dominant sugar type (N-Glycan) on membrane proteins on a cell surface. The variation helps stabilize these proteins and facilitate their functioning.

The researchers verified their observation of a between the number of sugars on a glycoprotein and its function in five animal species – worms, flies, fish, mice and humans. This led to their realization that the has been conserved through evolution.

To obtain the number of N-Glycans on proteins, the researchers used proteomics – a combination of mass spectrometry (MS) and high-performance liquid chromatography (HPLC). In less than an hour, high-throughput technique identifies the exact place where N-Glycans attach on hundreds of glycoproteins.

The scientists analyzed in one type of mouse embryonic stem cells by genetically shutting down the Hypoxanthine Phosphoribosyltransferase (HPRT) gene in the cells.

As an aside, HPRT deficiency causes Lesch-Nyhan syndrome in humans, a metabolic disorder characterized by mental retardation and self-mutilation.

Sun says this deeper understanding of the correlation between sugars’ positioning on glycoproteins and the proteins’ functions will benefit medical researchers and the pharmaceutical industry.

“As membrane proteins, glycoproteins are biologically important,” explains Sun, who is fluent in Mandarin and English, and is originally from Mailand China.

“They mediate cells’ communication to their environment, thus governing a plethora of cellular processes and functions, including growth, development, immunity and aging.

“Understanding how membrane proteins adapt to better protect themselves will help us design better, less toxic drugs to treat diseases.”


* http://dx.plos.org/10.1371/journal.pone.0055722
Simon Fraser University