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Mechanisms of Coupling Between Angiotensin Converting Enzyme 2 and Nicotinic Acetylcholine Receptors

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Mechanisms of Coupling Between Angiotensin Converting Enzyme 2 and Nicotinic Acetylcholine Receptors bioRxiv preprint doi: https://doi.org/10.1101/2021.08.12.456154; this version posted August 12, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Mechanisms of Coupling between Angiotensin Converting Enzyme 2 and Nicotinic Acetylcholine Receptors Nadine Kabbani1*, Kyle D. Brumfield2,3*, Patricia Sinclair4, Arvind Ramanathan5, Menu Leddy6, Rita R. Colwell2,3, and James L Olds7 1 School of Systems Biology, George Mason University; 2 University of Maryland Institute for Advanced Computer Studies, University of Maryland; 3 Maryland Pathogen Research Institute, University of Maryland; 4 Interdiscplinary Program in Neuroscience, George Mason University; 5 Argonne National Laboratory, University of Chicago; 6 Essential Environmental and Engineering Systems, 7 Schar School for Policy and Governance, George Mason University *NK and KB contributed equally to this work. Correspondence: Nadine Kabbani, 4400 University Drive, Fairfax, VA 22030, USA [email protected] Running Title: ACE2 binds the nicotinic receptor Key words: Virus; Toxin; Protein Evolution; Lipid Raft; Angiotensin Converting Enzyme 2; COVID-19; Nicotinic Acetylcholine Receptor; SARS-CoV-2 Abbreviations: nAChRs, Nicotinic Acetylcholine Receptor; ACE2, angiotensin converting enzyme 2; ACh, acetylcholine; Bgtx, α-bungarotoxin; CNS, central nervous system; Co-IP,co- immunoprecipitation; COVID-19, coronavirus disease 2019; Cryo-EM, cryogenic electron microscopy; Ctx, cholera toxin; fBgtx, fluorescent conjugated α-bungarotoxin; CytoB, cytochalasin B; MβCD, methyl-β-cyclodextrin; NGF, nerve growth factor; PC12, pheochromocytoma cell line 12; RBD, receptor binding domain; RBVG, rabies virus bioRxiv preprint doi: https://doi.org/10.1101/2021.08.12.456154; this version posted August 12, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. glycoprotein; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; S protein, Spike glycoprotein; TNFα, tumor necrosis factor α Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), an RNA virus encapsulated by a spike (S) glycoprotein envelope, binds with high affinity to angiotensin converting enzyme 2 (ACE2) during cell entry of a susceptible host. Recent studies suggest nicotinic acetylcholine receptors (nAChRs) play a role in functional ACE2 regulation and nicotine may contribute to the progression of coronavirus disease 2019 (COVID-19). Here, we present evidence for coupling between ACE2 and nAChR through bioinformatic analysis and cell culture experiments. Following molecular and structural protein comparison of over 250 ACE2 vertebrate orthologues, a region of human ACE2 at positions C542-L554 was identified to have sequence similarity to nAChR-binding neurotoxin and rabies virus glycoproteins (RBVG). Furthermore, experiments conducted in PC12 cells indicate a potential for physical interaction between ACE2 and α7 nAChR proteins. Our findings support a model of nAChR involvement in in COVID-19. Introduction In January 2020, an outbreak of SARS-CoV-2 led to the COVID-19 pandemic, resulting in nearly 170M confirmed cases globally by June 2021 [1]. Like other members of the β coronavirus family, this positive-stranded, enveloped RNA virus encodes an S glycoprotein that participates in host cell entry [2]. SARS-CoV-2 S binds with high affinity to ACE2 [3], a transmembrane metalloprotease that cleaves extracellular substrates and is itself subject to proteolytic cleavage [4][5]. While initially discovered as a second form of ACE within the mammalian renin angiotensin system (RAS) [6], orthologs of ACE2 have been reported in numerous species of the subphylum Vertebrata [7] and some insects—which do not contain a closed circulatory system [8,9]. Recent work has demonstrated that ferrets, cats, dogs, and select non-human primates are susceptible to SARS-CoV-2 infection [7,10,11]. However, the exact zoonotic tropisms of SARS-CoV-2 in humans remains elusive. 2 bioRxiv preprint doi: https://doi.org/10.1101/2021.08.12.456154; this version posted August 12, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Nicotine exposure, namely through the α7 nicotinic acetylcholine receptor (nAChR), has the potential to promote expression of ACE2 [12,13] and epidemiological surveillance has shown tobacco smokers present a varied response to SARS-CoV-2 infection and outcome [14]. However, the role of nicotine in SARS-CoV-2 infection remains speculative. Differential reports show contrasting lowered and increased number of hospitalizations across subsets of COVID-19 patients with a smoking history [12,15]. The nAChR is a well-characterized protein complex of the cys-loop channel family [16]. Activated by endogenous ligands, such as acetylcholine (ACh), nAChRs are also targeted by many plant and animal toxins [17]. Specifically, α7 nAChR signaling in immune cells can reduce inflammation via tumor necrosis factor α (TNFα) release [18,19]. It is worth noting that nicotine is known to impact the immune system [20], and interactions between nicotine exposure, cholinergic modulation, and ACE2 have been documented within RAS, as well as in neural systems [12,13,21]. ACE2 signaling in neurons and astrocytes can also contribute to oxidative stress and neuroinflammation in the context of Parkinson’s and Alzheimer’s disease [22]. We build on these observations to explore possible sites of interaction between ACE2 and α7 nAChR. Results of molecular bioinformatic analysis reveal a novel sequence domain within human ACE2 position C542-L554 that maintains noticeable sequence homology to several nAChR targeting toxin proteins as well as the rabies virus glycoprotein (RBVG). These findings are corroborated experimentally by evidence of protein coupling between α7 nAChR and ACE2 within cultured cells. Methods Amino Acid Sequence and Structure Analysis ACE2 amino acid sequences were compiled from the National Center for Biotechnology Information (NCBI) Reference [23] and the Universal Protein (UniProt) Knowledgebase [24] sequence databases for a total of 256 Animalia species of the subphylum Vertebrata, using a modified version of a database curated previously [25]. Amino acid sequences of ACE2 orthologues included in this study can be found in Supplementary File 1. Amino acid sequences were aligned globally using the MUltiple Sequence Comparison by Log-Expectation (MUSCLE) 3 bioRxiv preprint doi: https://doi.org/10.1101/2021.08.12.456154; this version posted August 12, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. software package v.3.8.31 with default parameters [26]. A phylogenetic bootstrap consensus tree was constructed from ACE2 alignments using the Molecular Evolutionary Genetics Analysis X (MEGAX) software packages v.10.1.8 [27] employing neighbor-joining method with 1,000 bootstrap replicates, as described previously [25]. Phylogenetic bootstrap consensus trees were visualized using the Interactive Tree of Life web server v.4 [28]. Patterns of ACE2 amino acid conservation across taxa and within accepted phylogenetic relationships were identified with respect to the human ACE2 amino acid sequence (UniProt: Q9BYF1) as reference using Jalview v.2.11.1.0 [29]. Putative common motifs were identified by comparing toxin protein sequences with the following UniProt identifiers (Alpha-cobratoxin, P01391; Alpha-bungarotoxin, P60615; and Long neurotoxin 3P25671) and Lyssavirus glycoproteins various isolates (ERA, P03524; CVS-11, O92284; Nishigahara RCEH, Q9IPJ6) to human ACE2 using Clustal Omega v.1.2.4 [30]. Human ACE2 at positions C542-L554, was identified by manually comparing conservation scores with 3D structural models predicted using the SWISS-MODEL web-based service [31] and visualized using PyMol Molecular Graphics System v.2.3.5 (Schrodinger, LLC, New York, NY, USA). To visualize hierarchical clustering of the ACE2 motifs across the species included in this study, a protein BLAST [32] Bit-score ratio (reference/query) was calculated for each protein sequence using human ACE2 as a reference. Cell Culture, drug treatment, and microscopy imaging The pheochromocytoma cell line 12 (PC12) was purchased from the American Type Culture Collection (CRL1721™; ATCC, Gaithersburg, MD, USA) and grown under standard conditions on a collagen (Santa Cruz, Dallas, TX, USA) coated matrix (50 μg/ml). PC12 cells were grown in Roswell Park Memorial Institute (RPMI) 1640 medium (ThermoFisher, Waltham, MA, USA) supplemented with horse serum (10% v/v), fetal bovine serum (5% v/v), and Penicillin-Streptomycin (1% v/v). Prior to experimentation (3 days), cells were differentiated using 200 ng/ml 2.5S mouse nerve growth factor (NGF; Millipore, Temecula, CA, USA) (200 ng/ml), as previously described in [33,34]. To test for protein-protein interactions, cells were treated with the following compounds (reconstituted fresh
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