Compound Uptake into E. coli Can Be Facilitated by N -Alkyl Guanidiniums and Pyridiniums
Multidrug-resistant Gram-negative bacterial infections are on the rise, and with no FDA approvals for new classes of broad-spectrum antibiotics in over 50 years, these infections constitute a major threat to human health. A significant challenge is the inability of most compounds to accumulate in Gr...
Gespeichert in:
Veröffentlicht in: | ACS infectious diseases 2021-01, Vol.7 (1), p.162-173 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 173 |
---|---|
container_issue | 1 |
container_start_page | 162 |
container_title | ACS infectious diseases |
container_volume | 7 |
creator | Perlmutter, Sarah J Geddes, Emily J Drown, Bryon S Motika, Stephen E Lee, Myung Ryul Hergenrother, Paul J |
description | Multidrug-resistant Gram-negative bacterial infections are on the rise, and with no FDA approvals for new classes of broad-spectrum antibiotics in over 50 years, these infections constitute a major threat to human health. A significant challenge is the inability of most compounds to accumulate in Gram-negative bacteria. Recently developed predictive guidelines show that appending a primary amine to an appropriately shaped compound can enhance Gram-negative accumulation. Here, we report that other positively charged nitrogen functional groups, namely,
-alkyl guanidiniums and pyridiniums, can also facilitate compound uptake into Gram-negative bacteria. The accumulation of a set of 60 nonantibiotic compounds, consisting of 20 primary amines and their corresponding guanidiniums and pyridiniums, was assessed in
. We also installed these alternate functional groups onto antibiotic scaffolds and assessed their accumulation and antibacterial activity in Gram-negative bacteria. The results suggest that other positively-charged, nitrogen-containing functional groups should be considered when designing antibiotics with Gram-negative activity. |
doi_str_mv | 10.1021/acsinfecdis.0c00715 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7796962</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2464148018</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3205-3656422a9cb97888f8b958779e4806513c8599804c7e130d382359e0b2c968d53</originalsourceid><addsrcrecordid>eNpVUd1KwzAUDqK4MfcEguTSm878NG1yI8yxTWGoF-7Cq5Cmmca1yWxaoW_js_hkVvbDvDrncL4_-AC4xGiEEcE3SgfrVkbnNoyQRijF7AT0CU1pxAlJT4_2HhiG8IEQwpSzOGbnoEcpIZyypA9eJ77c-MblcLmp1dpA62oPp6Ofb-0LCyfKwTsDZ0rbwtaqNjnMWvgIo3Gxbgs4b5SzuXW2KQNUnchzW-3vC3C2UkUww90cgOVs-jK5jxZP84fJeBFpShCLaMKSmBAldCZSzvmKZ4LxNBUm5ihhmGrOhOAo1qnBFOWUE8qEQRnRIuE5owNwu9XdNFlpcm1cXalCbipbqqqVXln5_-Psu3zzX7LzSERCOoHrnUDlPxsTalnaoE1RKGd8EySJkxh3YTDvoHQL1ZUPoTKrgw1G8q8XedSL3PXSsa6OEx44-xboL-G7i7Y</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2464148018</pqid></control><display><type>article</type><title>Compound Uptake into E. coli Can Be Facilitated by N -Alkyl Guanidiniums and Pyridiniums</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Perlmutter, Sarah J ; Geddes, Emily J ; Drown, Bryon S ; Motika, Stephen E ; Lee, Myung Ryul ; Hergenrother, Paul J</creator><creatorcontrib>Perlmutter, Sarah J ; Geddes, Emily J ; Drown, Bryon S ; Motika, Stephen E ; Lee, Myung Ryul ; Hergenrother, Paul J</creatorcontrib><description>Multidrug-resistant Gram-negative bacterial infections are on the rise, and with no FDA approvals for new classes of broad-spectrum antibiotics in over 50 years, these infections constitute a major threat to human health. A significant challenge is the inability of most compounds to accumulate in Gram-negative bacteria. Recently developed predictive guidelines show that appending a primary amine to an appropriately shaped compound can enhance Gram-negative accumulation. Here, we report that other positively charged nitrogen functional groups, namely,
-alkyl guanidiniums and pyridiniums, can also facilitate compound uptake into Gram-negative bacteria. The accumulation of a set of 60 nonantibiotic compounds, consisting of 20 primary amines and their corresponding guanidiniums and pyridiniums, was assessed in
. We also installed these alternate functional groups onto antibiotic scaffolds and assessed their accumulation and antibacterial activity in Gram-negative bacteria. The results suggest that other positively-charged, nitrogen-containing functional groups should be considered when designing antibiotics with Gram-negative activity.</description><identifier>ISSN: 2373-8227</identifier><identifier>EISSN: 2373-8227</identifier><identifier>DOI: 10.1021/acsinfecdis.0c00715</identifier><identifier>PMID: 33228356</identifier><language>eng</language><publisher>United States</publisher><subject>Anti-Bacterial Agents - pharmacology ; Anti-Bacterial Agents - therapeutic use ; Escherichia coli ; Gram-Negative Bacteria ; Gram-Negative Bacterial Infections - drug therapy ; Guanidine ; Humans</subject><ispartof>ACS infectious diseases, 2021-01, Vol.7 (1), p.162-173</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3205-3656422a9cb97888f8b958779e4806513c8599804c7e130d382359e0b2c968d53</citedby><cites>FETCH-LOGICAL-c3205-3656422a9cb97888f8b958779e4806513c8599804c7e130d382359e0b2c968d53</cites><orcidid>0000-0001-9018-3581</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,2766,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33228356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Perlmutter, Sarah J</creatorcontrib><creatorcontrib>Geddes, Emily J</creatorcontrib><creatorcontrib>Drown, Bryon S</creatorcontrib><creatorcontrib>Motika, Stephen E</creatorcontrib><creatorcontrib>Lee, Myung Ryul</creatorcontrib><creatorcontrib>Hergenrother, Paul J</creatorcontrib><title>Compound Uptake into E. coli Can Be Facilitated by N -Alkyl Guanidiniums and Pyridiniums</title><title>ACS infectious diseases</title><addtitle>ACS Infect Dis</addtitle><description>Multidrug-resistant Gram-negative bacterial infections are on the rise, and with no FDA approvals for new classes of broad-spectrum antibiotics in over 50 years, these infections constitute a major threat to human health. A significant challenge is the inability of most compounds to accumulate in Gram-negative bacteria. Recently developed predictive guidelines show that appending a primary amine to an appropriately shaped compound can enhance Gram-negative accumulation. Here, we report that other positively charged nitrogen functional groups, namely,
-alkyl guanidiniums and pyridiniums, can also facilitate compound uptake into Gram-negative bacteria. The accumulation of a set of 60 nonantibiotic compounds, consisting of 20 primary amines and their corresponding guanidiniums and pyridiniums, was assessed in
. We also installed these alternate functional groups onto antibiotic scaffolds and assessed their accumulation and antibacterial activity in Gram-negative bacteria. The results suggest that other positively-charged, nitrogen-containing functional groups should be considered when designing antibiotics with Gram-negative activity.</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Escherichia coli</subject><subject>Gram-Negative Bacteria</subject><subject>Gram-Negative Bacterial Infections - drug therapy</subject><subject>Guanidine</subject><subject>Humans</subject><issn>2373-8227</issn><issn>2373-8227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUd1KwzAUDqK4MfcEguTSm878NG1yI8yxTWGoF-7Cq5Cmmca1yWxaoW_js_hkVvbDvDrncL4_-AC4xGiEEcE3SgfrVkbnNoyQRijF7AT0CU1pxAlJT4_2HhiG8IEQwpSzOGbnoEcpIZyypA9eJ77c-MblcLmp1dpA62oPp6Ofb-0LCyfKwTsDZ0rbwtaqNjnMWvgIo3Gxbgs4b5SzuXW2KQNUnchzW-3vC3C2UkUww90cgOVs-jK5jxZP84fJeBFpShCLaMKSmBAldCZSzvmKZ4LxNBUm5ihhmGrOhOAo1qnBFOWUE8qEQRnRIuE5owNwu9XdNFlpcm1cXalCbipbqqqVXln5_-Psu3zzX7LzSERCOoHrnUDlPxsTalnaoE1RKGd8EySJkxh3YTDvoHQL1ZUPoTKrgw1G8q8XedSL3PXSsa6OEx44-xboL-G7i7Y</recordid><startdate>20210108</startdate><enddate>20210108</enddate><creator>Perlmutter, Sarah J</creator><creator>Geddes, Emily J</creator><creator>Drown, Bryon S</creator><creator>Motika, Stephen E</creator><creator>Lee, Myung Ryul</creator><creator>Hergenrother, Paul J</creator><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><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9018-3581</orcidid></search><sort><creationdate>20210108</creationdate><title>Compound Uptake into E. coli Can Be Facilitated by N -Alkyl Guanidiniums and Pyridiniums</title><author>Perlmutter, Sarah J ; Geddes, Emily J ; Drown, Bryon S ; Motika, Stephen E ; Lee, Myung Ryul ; Hergenrother, Paul J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3205-3656422a9cb97888f8b958779e4806513c8599804c7e130d382359e0b2c968d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Escherichia coli</topic><topic>Gram-Negative Bacteria</topic><topic>Gram-Negative Bacterial Infections - drug therapy</topic><topic>Guanidine</topic><topic>Humans</topic><toplevel>online_resources</toplevel><creatorcontrib>Perlmutter, Sarah J</creatorcontrib><creatorcontrib>Geddes, Emily J</creatorcontrib><creatorcontrib>Drown, Bryon S</creatorcontrib><creatorcontrib>Motika, Stephen E</creatorcontrib><creatorcontrib>Lee, Myung Ryul</creatorcontrib><creatorcontrib>Hergenrother, Paul J</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>ACS infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perlmutter, Sarah J</au><au>Geddes, Emily J</au><au>Drown, Bryon S</au><au>Motika, Stephen E</au><au>Lee, Myung Ryul</au><au>Hergenrother, Paul J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Compound Uptake into E. coli Can Be Facilitated by N -Alkyl Guanidiniums and Pyridiniums</atitle><jtitle>ACS infectious diseases</jtitle><addtitle>ACS Infect Dis</addtitle><date>2021-01-08</date><risdate>2021</risdate><volume>7</volume><issue>1</issue><spage>162</spage><epage>173</epage><pages>162-173</pages><issn>2373-8227</issn><eissn>2373-8227</eissn><abstract>Multidrug-resistant Gram-negative bacterial infections are on the rise, and with no FDA approvals for new classes of broad-spectrum antibiotics in over 50 years, these infections constitute a major threat to human health. A significant challenge is the inability of most compounds to accumulate in Gram-negative bacteria. Recently developed predictive guidelines show that appending a primary amine to an appropriately shaped compound can enhance Gram-negative accumulation. Here, we report that other positively charged nitrogen functional groups, namely,
-alkyl guanidiniums and pyridiniums, can also facilitate compound uptake into Gram-negative bacteria. The accumulation of a set of 60 nonantibiotic compounds, consisting of 20 primary amines and their corresponding guanidiniums and pyridiniums, was assessed in
. We also installed these alternate functional groups onto antibiotic scaffolds and assessed their accumulation and antibacterial activity in Gram-negative bacteria. The results suggest that other positively-charged, nitrogen-containing functional groups should be considered when designing antibiotics with Gram-negative activity.</abstract><cop>United States</cop><pmid>33228356</pmid><doi>10.1021/acsinfecdis.0c00715</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9018-3581</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2373-8227 |
ispartof | ACS infectious diseases, 2021-01, Vol.7 (1), p.162-173 |
issn | 2373-8227 2373-8227 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7796962 |
source | MEDLINE; American Chemical Society Journals |
subjects | Anti-Bacterial Agents - pharmacology Anti-Bacterial Agents - therapeutic use Escherichia coli Gram-Negative Bacteria Gram-Negative Bacterial Infections - drug therapy Guanidine Humans |
title | Compound Uptake into E. coli Can Be Facilitated by N -Alkyl Guanidiniums and Pyridiniums |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T04%3A09%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Compound%20Uptake%20into%20E.%C2%A0coli%20Can%20Be%20Facilitated%20by%20N%20-Alkyl%20Guanidiniums%20and%20Pyridiniums&rft.jtitle=ACS%20infectious%20diseases&rft.au=Perlmutter,%20Sarah%20J&rft.date=2021-01-08&rft.volume=7&rft.issue=1&rft.spage=162&rft.epage=173&rft.pages=162-173&rft.issn=2373-8227&rft.eissn=2373-8227&rft_id=info:doi/10.1021/acsinfecdis.0c00715&rft_dat=%3Cproquest_pubme%3E2464148018%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2464148018&rft_id=info:pmid/33228356&rfr_iscdi=true |