A molecule responsible for ending the activity of an enzyme essential to the Middle East Respiratory Syndrome (MERS) virus replication has been identified by researchers, including an Indian-origin.
The virus is in the international spotlight again as South Korea faces the largest MERS outbreak outside the Middle East.
More than 2,800 people have been quarantined during the outbreak. The World Health Organization (WHO) reported 27 deaths and 172 confirmed cases in its most recent update on June 22.
Professors Arun Ghosh and Andrew Mesecar from Purdue University in the US have been studying the virus and creating and testing molecular compounds that could lead to potential treatments since shortly after MERS was discovered.
"The team identified molecules that inhibit an enzyme essential to MERS virus replication and discovered a characteristic of the enzyme that is very different from other coronaviruses, the family of viruses to which MERS-CoV belongs," Mesecar said.
"This enzyme is a prime target - an Achilles' heel of the virus."
The team was targeting an enzyme within the MERS virus called 3C-like protease, without which the virus cannot create more viruses to further an infection.
"We captured the protease's atomic structure through this work, which provides the map to design potent new drugs to fight MERS," said Mesecar.
The MERS virus emerged in 2012 and was mostly confined to the Middle East until 2014 when cases were identified in the US, Britain, France and Italy. Till date, 25 countries have reported cases, according to the WHO.
"It is a threat to public health and there currently is no treatment or vaccine. We continue to study the virus to improve our understanding of how it works and ways to prevent its spread."
The study was published in the Journal of Biological Chemistry.