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A team of scientists has identified a molecule in which the key molecule is an octa-octa-proton as a mechanism that could aid in the development of therapeutics for multiple sclerosis (MS).

The researchers found that by injecting the same molecule in two different human cell lines, there is no difference in the ability of the two to produce a protective anti-MS protein. In addition, when the researchers put a human immune cell line into these cells, the resulting cell showed a protective antibody to the molecule.

Professor David Healy, chair of the Department of Molecular Bioscience and Bioinformatics at the University of Auckland, said the findings indicated that the molecule, known as CHOP, might be a new drug target for MS. “It is one of the few molecules which we know produces protection against antibodies to the virus and that may be one of its functions”, he said.

Professor Healy, Professor Michael McEwen from the University of Otago, Dr Michael Collins from the University of Otago and Professor Stephen Pearsall from the University of Canterbury identified the molecule in October 2014 in the laboratory of Professor Richard Stansfield.

Dr Collins said the study showed how the molecules can work synergistically to shield both the body and the viruses when tested in the cell line with MS. He said: “It is possible this molecule will be used as a new therapeutic target for MS.”

The research has been published in the online edition of journal Nature Communications.

The next time you see an ad for a car show, it might take you into your own life.

For a limited time, the Chrysler/Jeep Jeep Grand Cherokee is on sale for “the next 60 years.” It does not include a loan or loan-to-own option, which is a good indication of its true value.

“We are all in that 60-year range,” said John W. Brown, chief executive officer of Chrysler. “That’s the real value. That you’d think would be something that would get people excited.”

Chrysler sold about 14,500 Cherokee sedans last year, which was the fastest Jeep sales year ever.

As part of the deal, the ad will run in both North American and Canadian media starting Wednesday. The ads will then run across various digital platforms,

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