Carbonic anhydrase II does not exhibit Nitrite reductase or Nitrous Anhydrase Activity

Carbonic anhydrase II (CA II) is a zinc metalloenzyme that catalyzes the reversible interconversion of water and CO2 to bicarbonate and a proton. CA II is abundant in most cells, and plays a role in numerous processes including gas exchange, epithelial ion transport, respiration, extra- and intracel...

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Veröffentlicht in:Free radical biology & medicine 2018-03, Vol.117, p.1-5
Hauptverfasser: Andring, Jacob T., Lomelino, Carrie L., Tu, Chingkuang, Silverman, David N., McKenna, Robert, Swenson, Erik R.
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container_title Free radical biology & medicine
container_volume 117
creator Andring, Jacob T.
Lomelino, Carrie L.
Tu, Chingkuang
Silverman, David N.
McKenna, Robert
Swenson, Erik R.
description Carbonic anhydrase II (CA II) is a zinc metalloenzyme that catalyzes the reversible interconversion of water and CO2 to bicarbonate and a proton. CA II is abundant in most cells, and plays a role in numerous processes including gas exchange, epithelial ion transport, respiration, extra- and intracellular pH control, and vascular regulation. Beyond these CO2 and pH-linked roles, it has been postulated that CA II might also reduce nitrite (NO2-) to nitric oxide (NO), as bicarbonate and NO2- both exhibit sp2 molecular geometry and NO also plays an important role in vasodilation and regulation of blood pressure. Indeed, previous studies by Aamand et al. have shown that bovine CA II (BCA II) possesses nitrite dehydration activity and paradoxically demonstrated that CA inhibitors (CAIs) such as dorzolamide and acetazolamide significantly increased NO production (Aamand et al., 2009; Nielsen and Fago, 2015) [1,2]. Hence, the goal of this work was to revisit these studies using the same experimental conditions as Aamand et al. measuring NO generation by two methods, and to examine the structure of CA II in complex with NO2- in the presence and absence of dorzolamide. Our results contradict the previous findings and indicate that CA II does not exhibit nitrite reductase or dehydration activity, and that this is not enhanced in the presence of CA inhibitors. In addition, a structural examination of BCA II in complex with NO2- and superimposed with dorzolamide demonstrates that CA inhibitor binding at the active site to the zinc moiety blocks potential NO2- binding. [Display omitted] •Membrane inlet mass spectrometry and NO electrode measurements show tCA has no nitrite reductase or nitrous anhydrase activity.•There is no potentiation of CA-mediated nitrite reductase or nitrous anhydrase activity by the CA inhibitor, dorzolamide.•Structural examination of the CA II active site shows no ability to bind nitrite to the zinc in the presence of dorzolamide.
doi_str_mv 10.1016/j.freeradbiomed.2018.01.015
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CA II is abundant in most cells, and plays a role in numerous processes including gas exchange, epithelial ion transport, respiration, extra- and intracellular pH control, and vascular regulation. Beyond these CO2 and pH-linked roles, it has been postulated that CA II might also reduce nitrite (NO2-) to nitric oxide (NO), as bicarbonate and NO2- both exhibit sp2 molecular geometry and NO also plays an important role in vasodilation and regulation of blood pressure. Indeed, previous studies by Aamand et al. have shown that bovine CA II (BCA II) possesses nitrite dehydration activity and paradoxically demonstrated that CA inhibitors (CAIs) such as dorzolamide and acetazolamide significantly increased NO production (Aamand et al., 2009; Nielsen and Fago, 2015) [1,2]. Hence, the goal of this work was to revisit these studies using the same experimental conditions as Aamand et al. measuring NO generation by two methods, and to examine the structure of CA II in complex with NO2- in the presence and absence of dorzolamide. Our results contradict the previous findings and indicate that CA II does not exhibit nitrite reductase or dehydration activity, and that this is not enhanced in the presence of CA inhibitors. In addition, a structural examination of BCA II in complex with NO2- and superimposed with dorzolamide demonstrates that CA inhibitor binding at the active site to the zinc moiety blocks potential NO2- binding. [Display omitted] •Membrane inlet mass spectrometry and NO electrode measurements show tCA has no nitrite reductase or nitrous anhydrase activity.•There is no potentiation of CA-mediated nitrite reductase or nitrous anhydrase activity by the CA inhibitor, dorzolamide.•Structural examination of the CA II active site shows no ability to bind nitrite to the zinc in the presence of dorzolamide.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2018.01.015</identifier><identifier>PMID: 29355738</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Carbonic anhydrase II ; Carbonic Anhydrase II - chemistry ; Cattle ; Crystallography, X-Ray ; Dinitrogen trioxide ; Nitrite ; Nitrite reductase ; Nitrite Reductases - chemistry ; Nitrous acid ; Nitrous anhydrase ; Oxidoreductases - chemistry</subject><ispartof>Free radical biology &amp; medicine, 2018-03, Vol.117, p.1-5</ispartof><rights>2018</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-17b2bbc1d8c93acc8833cfd722bfe3f4101d589dc54b7ebee18d904345b3e2473</citedby><cites>FETCH-LOGICAL-c383t-17b2bbc1d8c93acc8833cfd722bfe3f4101d589dc54b7ebee18d904345b3e2473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S089158491830025X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29355738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andring, Jacob T.</creatorcontrib><creatorcontrib>Lomelino, Carrie L.</creatorcontrib><creatorcontrib>Tu, Chingkuang</creatorcontrib><creatorcontrib>Silverman, David N.</creatorcontrib><creatorcontrib>McKenna, Robert</creatorcontrib><creatorcontrib>Swenson, Erik R.</creatorcontrib><title>Carbonic anhydrase II does not exhibit Nitrite reductase or Nitrous Anhydrase Activity</title><title>Free radical biology &amp; medicine</title><addtitle>Free Radic Biol Med</addtitle><description>Carbonic anhydrase II (CA II) is a zinc metalloenzyme that catalyzes the reversible interconversion of water and CO2 to bicarbonate and a proton. 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[Display omitted] •Membrane inlet mass spectrometry and NO electrode measurements show tCA has no nitrite reductase or nitrous anhydrase activity.•There is no potentiation of CA-mediated nitrite reductase or nitrous anhydrase activity by the CA inhibitor, dorzolamide.•Structural examination of the CA II active site shows no ability to bind nitrite to the zinc in the presence of dorzolamide.</description><subject>Animals</subject><subject>Carbonic anhydrase II</subject><subject>Carbonic Anhydrase II - chemistry</subject><subject>Cattle</subject><subject>Crystallography, X-Ray</subject><subject>Dinitrogen trioxide</subject><subject>Nitrite</subject><subject>Nitrite reductase</subject><subject>Nitrite Reductases - chemistry</subject><subject>Nitrous acid</subject><subject>Nitrous anhydrase</subject><subject>Oxidoreductases - chemistry</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1LAzEQhoMotlb_gix48bI12STdBE-lVC0UvajXsElmaUq7qUkq9t-7a1vBmzAwMPO88_EidEPwkGAyulsO6wAQKqudX4MdFpiIISZt8BPUJ6KkOeNydIr6WEiSc8FkD13EuMQYM07FOeoVknJeUtFH75MqaN84k1XNYmdDFSGbzTLrIWaNTxl8LZx2KXt2KbgEWQC7NamjfPgp-m3Mxr_SsUnu06XdJTqrq1WEq0MeoLeH6evkKZ-_PM4m43luqKApJ6UutDbECiNpZYwQlJralkWha6A1a_-1XEhrONMlaAAirMSMMq4pFKykA3S7n7sJ_mMLMam1iwZWq6qB9jJFpJCSMM5Ii97vURN8jAFqtQluXYWdIlh1xqql-mOs6oxVmLTBW_X1YdFWd72j9uhkC0z3ALTvfjoIKhoHjQHrApikrHf_WvQN5WySiA</recordid><startdate>201803</startdate><enddate>201803</enddate><creator>Andring, Jacob T.</creator><creator>Lomelino, Carrie L.</creator><creator>Tu, Chingkuang</creator><creator>Silverman, David N.</creator><creator>McKenna, Robert</creator><creator>Swenson, Erik R.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201803</creationdate><title>Carbonic anhydrase II does not exhibit Nitrite reductase or Nitrous Anhydrase Activity</title><author>Andring, Jacob T. ; Lomelino, Carrie L. ; Tu, Chingkuang ; Silverman, David N. ; McKenna, Robert ; Swenson, Erik R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-17b2bbc1d8c93acc8833cfd722bfe3f4101d589dc54b7ebee18d904345b3e2473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Carbonic anhydrase II</topic><topic>Carbonic Anhydrase II - chemistry</topic><topic>Cattle</topic><topic>Crystallography, X-Ray</topic><topic>Dinitrogen trioxide</topic><topic>Nitrite</topic><topic>Nitrite reductase</topic><topic>Nitrite Reductases - chemistry</topic><topic>Nitrous acid</topic><topic>Nitrous anhydrase</topic><topic>Oxidoreductases - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andring, Jacob T.</creatorcontrib><creatorcontrib>Lomelino, Carrie L.</creatorcontrib><creatorcontrib>Tu, Chingkuang</creatorcontrib><creatorcontrib>Silverman, David N.</creatorcontrib><creatorcontrib>McKenna, Robert</creatorcontrib><creatorcontrib>Swenson, Erik R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Free radical biology &amp; medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andring, Jacob T.</au><au>Lomelino, Carrie L.</au><au>Tu, Chingkuang</au><au>Silverman, David N.</au><au>McKenna, Robert</au><au>Swenson, Erik R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbonic anhydrase II does not exhibit Nitrite reductase or Nitrous Anhydrase Activity</atitle><jtitle>Free radical biology &amp; medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2018-03</date><risdate>2018</risdate><volume>117</volume><spage>1</spage><epage>5</epage><pages>1-5</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>Carbonic anhydrase II (CA II) is a zinc metalloenzyme that catalyzes the reversible interconversion of water and CO2 to bicarbonate and a proton. 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Hence, the goal of this work was to revisit these studies using the same experimental conditions as Aamand et al. measuring NO generation by two methods, and to examine the structure of CA II in complex with NO2- in the presence and absence of dorzolamide. Our results contradict the previous findings and indicate that CA II does not exhibit nitrite reductase or dehydration activity, and that this is not enhanced in the presence of CA inhibitors. In addition, a structural examination of BCA II in complex with NO2- and superimposed with dorzolamide demonstrates that CA inhibitor binding at the active site to the zinc moiety blocks potential NO2- binding. [Display omitted] •Membrane inlet mass spectrometry and NO electrode measurements show tCA has no nitrite reductase or nitrous anhydrase activity.•There is no potentiation of CA-mediated nitrite reductase or nitrous anhydrase activity by the CA inhibitor, dorzolamide.•Structural examination of the CA II active site shows no ability to bind nitrite to the zinc in the presence of dorzolamide.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29355738</pmid><doi>10.1016/j.freeradbiomed.2018.01.015</doi><tpages>5</tpages></addata></record>
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subjects Animals
Carbonic anhydrase II
Carbonic Anhydrase II - chemistry
Cattle
Crystallography, X-Ray
Dinitrogen trioxide
Nitrite
Nitrite reductase
Nitrite Reductases - chemistry
Nitrous acid
Nitrous anhydrase
Oxidoreductases - chemistry
title Carbonic anhydrase II does not exhibit Nitrite reductase or Nitrous Anhydrase Activity
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