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Hot Spot Mutagenesis Improves the Functional Expression of Unique Mammalian Odorant Receptors
Vertebrate animals detect odors through olfactory receptors (ORs), members of the G protein-coupled receptor (GPCR) family. Due to the difficulty in the heterologous expression of ORs, studies of their odor molecule recognition mechanisms have progressed poorly. Functional expression of most ORs in...
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Published in: | International journal of molecular sciences 2021-12, Vol.23 (1), p.277 |
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creator | Fukutani, Yosuke Nakamura, Yuko Muto, Nonoko Miyanaga, Shunta Kanemaki, Reina Ikegami, Kentaro Noguchi, Keiichi Ohsawa, Ikuroh Matsunami, Hiroaki Yohda, Masafumi |
description | Vertebrate animals detect odors through olfactory receptors (ORs), members of the G protein-coupled receptor (GPCR) family. Due to the difficulty in the heterologous expression of ORs, studies of their odor molecule recognition mechanisms have progressed poorly. Functional expression of most ORs in heterologous cells requires the co-expression of their chaperone proteins, receptor transporting proteins (RTPs). Yet, some ORs were found to be functionally expressed without the support of RTP (RTP-independent ORs). In this study, we investigated whether amino acid residues highly conserved among RTP-independent ORs improve the functional expression of ORs in heterologous cells. We found that a single amino acid substitution at one of two sites (N
3.39 and 3.43) in their conserved residues (E and L, respectively) significantly improved the functional expression of ORs in heterologous cells. E
and L
also enhanced the membrane expression of RTP-dependent ORs in the absence of RTP. These changes did not alter the odorant responsiveness of the tested ORs. Our results showed that specific sites within transmembrane domains regulate the membrane expression of some ORs. |
doi_str_mv | 10.3390/ijms23010277 |
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3.39 and 3.43) in their conserved residues (E and L, respectively) significantly improved the functional expression of ORs in heterologous cells. E
and L
also enhanced the membrane expression of RTP-dependent ORs in the absence of RTP. These changes did not alter the odorant responsiveness of the tested ORs. Our results showed that specific sites within transmembrane domains regulate the membrane expression of some ORs.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23010277</identifier><identifier>PMID: 35008703</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Amino acid substitution ; Amino acids ; Amino Acids - genetics ; Animals ; Binding sites ; G protein-coupled receptors ; Gene Expression Regulation ; HEK293 Cells ; Humans ; Ligands ; Loss of Function Mutation - genetics ; Mammals - genetics ; Membranes ; Mice ; Mutagenesis ; Mutagenesis - genetics ; Mutant Proteins - metabolism ; Mutation ; Mutation - genetics ; Odor recognition ; Odorant receptors ; Odors ; Protein transport ; Proteins ; Receptors, Odorant - agonists ; Receptors, Odorant - chemistry ; Receptors, Odorant - genetics ; Residues ; Sodium ; Transmembrane domains ; Vertebrates</subject><ispartof>International journal of molecular sciences, 2021-12, Vol.23 (1), p.277</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-3fcf106d0334c6e32273809bba8d70f1aa19e622ea7ee1223259f517f931dfcb3</citedby><cites>FETCH-LOGICAL-c478t-3fcf106d0334c6e32273809bba8d70f1aa19e622ea7ee1223259f517f931dfcb3</cites><orcidid>0000-0001-8307-9671 ; 0000-0002-3716-8590</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2618238577/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2618238577?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25733,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35008703$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fukutani, Yosuke</creatorcontrib><creatorcontrib>Nakamura, Yuko</creatorcontrib><creatorcontrib>Muto, Nonoko</creatorcontrib><creatorcontrib>Miyanaga, Shunta</creatorcontrib><creatorcontrib>Kanemaki, Reina</creatorcontrib><creatorcontrib>Ikegami, Kentaro</creatorcontrib><creatorcontrib>Noguchi, Keiichi</creatorcontrib><creatorcontrib>Ohsawa, Ikuroh</creatorcontrib><creatorcontrib>Matsunami, Hiroaki</creatorcontrib><creatorcontrib>Yohda, Masafumi</creatorcontrib><title>Hot Spot Mutagenesis Improves the Functional Expression of Unique Mammalian Odorant Receptors</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Vertebrate animals detect odors through olfactory receptors (ORs), members of the G protein-coupled receptor (GPCR) family. Due to the difficulty in the heterologous expression of ORs, studies of their odor molecule recognition mechanisms have progressed poorly. Functional expression of most ORs in heterologous cells requires the co-expression of their chaperone proteins, receptor transporting proteins (RTPs). Yet, some ORs were found to be functionally expressed without the support of RTP (RTP-independent ORs). In this study, we investigated whether amino acid residues highly conserved among RTP-independent ORs improve the functional expression of ORs in heterologous cells. We found that a single amino acid substitution at one of two sites (N
3.39 and 3.43) in their conserved residues (E and L, respectively) significantly improved the functional expression of ORs in heterologous cells. E
and L
also enhanced the membrane expression of RTP-dependent ORs in the absence of RTP. These changes did not alter the odorant responsiveness of the tested ORs. 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Due to the difficulty in the heterologous expression of ORs, studies of their odor molecule recognition mechanisms have progressed poorly. Functional expression of most ORs in heterologous cells requires the co-expression of their chaperone proteins, receptor transporting proteins (RTPs). Yet, some ORs were found to be functionally expressed without the support of RTP (RTP-independent ORs). In this study, we investigated whether amino acid residues highly conserved among RTP-independent ORs improve the functional expression of ORs in heterologous cells. We found that a single amino acid substitution at one of two sites (N
3.39 and 3.43) in their conserved residues (E and L, respectively) significantly improved the functional expression of ORs in heterologous cells. E
and L
also enhanced the membrane expression of RTP-dependent ORs in the absence of RTP. These changes did not alter the odorant responsiveness of the tested ORs. Our results showed that specific sites within transmembrane domains regulate the membrane expression of some ORs.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35008703</pmid><doi>10.3390/ijms23010277</doi><orcidid>https://orcid.org/0000-0001-8307-9671</orcidid><orcidid>https://orcid.org/0000-0002-3716-8590</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acid substitution Amino acids Amino Acids - genetics Animals Binding sites G protein-coupled receptors Gene Expression Regulation HEK293 Cells Humans Ligands Loss of Function Mutation - genetics Mammals - genetics Membranes Mice Mutagenesis Mutagenesis - genetics Mutant Proteins - metabolism Mutation Mutation - genetics Odor recognition Odorant receptors Odors Protein transport Proteins Receptors, Odorant - agonists Receptors, Odorant - chemistry Receptors, Odorant - genetics Residues Sodium Transmembrane domains Vertebrates |
title | Hot Spot Mutagenesis Improves the Functional Expression of Unique Mammalian Odorant Receptors |
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