{"id":2569,"date":"2023-11-09T02:48:54","date_gmt":"2023-11-09T02:48:54","guid":{"rendered":"https:\/\/healthliteracyasia.com\/id\/2023\/11\/09\/how-viruses-use-fake-proteins-to-hide-in-our-cells\/"},"modified":"2025-10-27T09:22:51","modified_gmt":"2025-10-27T09:22:51","slug":"how-viruses-use-fake-proteins-to-hide-in-our-cells","status":"publish","type":"post","link":"https:\/\/healthliteracyasia.com\/id\/2023\/11\/09\/how-viruses-use-fake-proteins-to-hide-in-our-cells\/","title":{"rendered":"How viruses use \u2018fake\u2019 proteins to hide in our cells"},"content":{"rendered":"\n

Some viruses can hide in our bodies for decades. They make \u2018fake\u2019 human proteins that trick our immune cells into thinking \u2018everything is awesome\u2019, there\u2019s nothing to see here.<\/p>\n\n\n\n

\n \n \"Research\n <\/a>\n<\/div>\n\n\n\n\n

Now, researchers at the Imaging Center of Excellence at Monash and Melbourne Universities have determined the basic structure of one of the two known families of these deceptive proteins.<\/p>\n\n\n\n

Using synchrotron light and working with a common virus that lives in people happily and, for the most part, harmlessly, they worked out the structure of the fake proteins. This is an important first step towards producing better vaccines and drugs to fight viral diseases.<\/p>\n\n\n\n

The research was posted online this week by the Journal of Biological Chemistry. It will appear in the September issue of the journal. The paper describes the structure of m04 immunoevasin from mouse cytomegalovirus, a member of the m02 protein family.<\/p>\n\n\n\n

Cytomegaloviruses belong to the herpesvirus family whose members can cause glandular fever, chicken pox, and cold sores. About half the population becomes infected with the virus, develops flu-like illness, and then carries the virus for life. But the virus can be dangerous to pregnant women and people whose immune system becomes suppressed.<\/p>\n\n\n\n

The mouse variant is an important model for understanding how this family of viruses can hide from our immune systems.<\/p>\n\n\n\n

\u201cOur work highlights how these viruses mimic the immune system in order to evade it,\u201d says Monash University\u2019s Dr Richard Berry, a senior author of the paper. He works in a research group led by Prof Jamie Rossjohn, the other senior author and a Chief Investigator of the Imaging Center.<\/p>\n\n\n\n

Mouse and human immune T-cells patrol our bodies, checking on the health of cells. One of the things they look for is a complex of proteins on the surface of cells. This major histocompatibility complex (MHC) presents a snapshot of what\u2019s inside the cell. If bits of viral protein are detected by the T cells, they flag the infected cell for destruction.<\/p>\n\n\n\n

Viruses fight back by disrupting the production of the MHC protein complex, thus reducing the numbers on the outer membrane.<\/p>\n\n\n\n

But then, the next stage of what could be described as an evolutionary arms race kicks in. If there are too few MHC proteins on the outer membrane of a cell, then a different type of immune cell, termed the natural killer cell, will kill the cell just to be safe.<\/p>\n\n\n\n

Cytomegaloviruses have responded to this by making large families of fake cellular proteins that interfere with natural killer cell recognition. It is the basic structure of one of these families that Rossjohn, Berry, and their colleagues have become the first researchers to reveal.<\/p>\n\n\n\n

\u201cIt\u2019s been a race against our international competitors, which we won with the help of the Australian Synchrotron,\u201d Rossjohn says. \u201cWe were only able to produce very small protein crystals from which to solve the structures\u2014too small to allow us to gain meaningful data with anything other than synchrotron X-rays.\u201d<\/p>\n\n\n\n

Source: RedOrbit<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

Some viruses can hide in our bodies for decades. They make \u2018fake\u2019 human proteins that trick our immune cells into thinking \u2018everything is awesome\u2019, there\u2019s nothing to see here. Now, researchers at the Imaging Center of Excellence at Monash and Melbourne Universities have determined the basic structure of one of the two known families of these deceptive proteins. Using synchrotron light and working with a common virus that lives in people happily and, for the most part, harmlessly, they worked out the structure of the fake proteins. This is an important first step towards producing better vaccines and drugs to fight viral diseases. The research was posted online this week by the Journal of Biological Chemistry. It will appear in the September issue of the journal. The paper describes the structure of m04 immunoevasin from mouse cytomegalovirus, a member of the m02 protein family. Cytomegaloviruses belong to the herpesvirus family whose members can cause glandular fever, chicken pox, and cold sores. About half the population becomes infected with the virus, develops flu-like illness, and then carries the virus for life. But the virus can be dangerous to pregnant women and people whose immune system becomes suppressed. The mouse variant is an important model for understanding how this family of viruses can hide from our immune systems. \u201cOur work highlights how these viruses mimic the immune system in order to evade it,\u201d says Monash University\u2019s Dr Richard Berry, a senior author of the paper. He works in a research group led by Prof Jamie Rossjohn, the other senior author and a Chief Investigator of the Imaging Center. Mouse and human immune T-cells patrol our bodies, checking on the health of cells. One of the things they look for is a complex of proteins on the surface of cells. This major histocompatibility complex (MHC) presents a snapshot of what\u2019s inside the cell. If bits of viral protein are detected by the T cells, they flag the infected cell for destruction. Viruses fight back by disrupting the production of the MHC protein complex, thus reducing the numbers on the outer membrane. But then, the next stage of what could be described as an evolutionary arms race kicks in. If there are too few MHC proteins on the outer membrane of a cell, then a different type of immune cell, termed the natural killer cell, will kill the cell just to be safe. Cytomegaloviruses have responded to this by making large families of fake cellular proteins that interfere with natural killer cell recognition. It is the basic structure of one of these families that Rossjohn, Berry, and their colleagues have become the first researchers to reveal. \u201cIt\u2019s been a race against our international competitors, which we won with the help of the Australian Synchrotron,\u201d Rossjohn says. \u201cWe were only able to produce very small protein crystals from which to solve the structures\u2014too small to allow us to gain meaningful data with anything other than synchrotron X-rays.\u201d Source: RedOrbit<\/p>\n","protected":false},"author":19,"featured_media":2570,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[71,1],"tags":[72,73,74,75,76,77,59],"class_list":["post-2569","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medical-literacy","category-news","tag-health","tag-immunization","tag-infection","tag-protein","tag-research","tag-t-cells","tag-virus"],"yoast_head":"\nHow viruses use \u2018fake\u2019 proteins to hide in our cells - 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