Novel protein interactions with ACE2 disrupted by SARS-CoV-2, contributes to COVID-19 pathologies

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The novel coronavirus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused severe morbidity and mortality across the world. Other than flu-like symptoms of respiratory disease, SARS-CoV-2 infection can also cause systemic manifestations, leading to a wide range of pathologies, including thrombosis and microvascular injury and stroke, vascular system disruption, gastrointestinal complications, ocular and dermatological symptoms, cardiac and kidney pathologies, neurological manifestations, male infertility, and a Kawasaki-like blood and heart disorder in children.

A severe and often fatal immune response called a “cytokine storm” can occur following SARS-CoV-2 infection. Some patients suffer from a range of complications several months after testing negative for SARS-CoV-2, and this is called ‘Long Haul’  or ‘Long’ COVID-19.  The causes behind this phenomenon are not well understood.

This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. Links to the preliminary and peer-reviewed reports are available in the Sources section at the bottom of this article. View Sources

The human ACE2 receptor and its role in SARS-CoV-2 entry into host cells

The angiotensin-converting enzyme 2 (ACE2), the primary receptor for entry of SARS-CoV-2 into human cells, also plays a role in blood pressure regulation and vasodilation by the renin-angiotensin system, and digestion of protein in the gut. The binding of SARS-CoV-2 to ACE2 leads to a downregulation in ACE2 function, which may be associated with systemic damage.

“Angiotensin-converting enzyme 2 (ACE2) is of obvious interest because it is a primary receptor for SARS-CoV-2 entry into human cells.”

Elevated soluble ACE2 levels have been found in severely ill COVID-19 patients, explaining the reduced expression of membrane-bound ACE2. According to a recent study, sACE2 may have a role in SARS-CoV-2 entry via other receptors.

ACE2 Unidirectional Reciprocal Rank (URR) Network. ACE2’s top 10 unidirectional ERC proteins for a web of reciprocal rank (RR20) connections. The network is particularly enriched for cytokine signaling and immunity. Highly interconnected proteins include COL4A5, F5, GEN1, and IFNAR2. ACE2 is highlighted in purple, and blue shading intensity indicates the level of reciprocal connectivity for different proteins.
ACE2 Unidirectional Reciprocal Rank (URR) Network. ACE2’s top 10 unidirectional ERC proteins for a web of reciprocal rank (RR20) connections. The network is particularly enriched for cytokine signaling and immunity. Highly interconnected proteins include COL4A5, F5, GEN1, and IFNAR2. ACE2 is highlighted in purple, and blue shading intensity indicates the level of reciprocal connectivity for different proteins.

A novel approach - evolutionary inference - to understanding protein-ACE2 s interactions

A better understanding of what kind of proteins ACE2 interacts with can shed light on disease manifestations and potential treatment avenues. Researchers from the US attempted a new approach to predict candidate proteins interacting with ACE2. They used evolutionary inference to identify a group of mammalian proteins that “coevolve” along with ACE2. This study is published on the bioRxiv* preprint server.

The novel approach is called evolutionary rate correlation (ERC), and it detects proteins with highly correlated evolutionary rates in mammalian evolution. These proteins can be good candidates for biological interactions with ACE2.

“Overall, the underlying concept behind the evolutionary rate coevolution concept (also called evolutionary rate covariance or evolutionary rate coevolution) is that coevolving proteins will show correlated rates of change across evolution and that this reflects functional interactions.”

The approach has revealed many fundamental ACE2-protein interactions which may be relevant to COVID-19 pathologies. While some proteins reported to be linked to severe COVID-19 are currently not known to interact with ACE2 directly, some other novel proteins interacting with ACE2 may be relevant to COVID-19.

ACE2 has strong connections to coagulation pathway proteins relevant to COVID-19 pathologies

With the help of reciprocal rankings of protein ERCs, the researchers identified strongly interconnected protein networks associated with ACE2 that are relevant to COVID-19 pathologies. The findings show that ACE2 has strong connections to coagulation pathway proteins, including coagulation factor V and fibrinogen components FGG, FGB, and FGA.

The fibrinogen components may mediate through ACE2 connections to clusterin, which removes misfolded extracellular proteins, and GPR141, functions of which are relatively not clear.

SARS-CoV-2 disrupts novel protein-ACE2 interactions contributing to COVID-19 pathologies

Moreover, ACE2 has links to proteins part of cytokine signaling and immune response such as IFNAR2, XCR1, and TLR8, and to the androgen receptor.  The ERC pre-screening approach has also clarified potential functions for some previously uncharacterized proteins and additional functions for some already well-characterized proteins.

The study also discussed validation approaches for ACE2 interacting proteins predicted by ERC. The authors propose that SARS-CoV-2 infection disrupts novel protein interactions of ACE2, which contributes to the wide range of COVID-19 pathologies.

“Finally, if evidence mounts that ERCs can be informative in predicting protein interactions, the approach can be applied more broadly as an additional tool for detecting protein interaction networks involved in biological processes and disease.”

This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. Links to the preliminary and peer-reviewed reports are available in the Sources section at the bottom of this article. View Sources

Journal references:

Article Revisions

  • Apr 8 2023 - The preprint preliminary research paper that this article was based upon was accepted for publication in a peer-reviewed Scientific Journal. This article was edited accordingly to include a link to the final peer-reviewed paper, now shown in the sources section.
Susha Cheriyedath

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Susha Cheriyedath

Susha is a scientific communication professional holding a Master's degree in Biochemistry, with expertise in Microbiology, Physiology, Biotechnology, and Nutrition. After a two-year tenure as a lecturer from 2000 to 2002, where she mentored undergraduates studying Biochemistry, she transitioned into editorial roles within scientific publishing. She has accumulated nearly two decades of experience in medical communication, assuming diverse roles in research, writing, editing, and editorial management.

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