Loading…

Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells

The development of more effective drugs requires knowledge of their bioavailability and binding efficacy directly in the native cellular environment. In-cell nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for investigating ligand–target interactions directly in living cells. Howeve...

Full description

Saved in:
Bibliographic Details
Published in:Journal of medicinal chemistry 2024-01, Vol.67 (2), p.1115-1126
Main Authors: Luchinat, Enrico, Barbieri, Letizia, Davis, Ben, Brough, Paul A., Pennestri, Matteo, Banci, Lucia
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 1126
container_issue 2
container_start_page 1115
container_title Journal of medicinal chemistry
container_volume 67
creator Luchinat, Enrico
Barbieri, Letizia
Davis, Ben
Brough, Paul A.
Pennestri, Matteo
Banci, Lucia
description The development of more effective drugs requires knowledge of their bioavailability and binding efficacy directly in the native cellular environment. In-cell nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for investigating ligand–target interactions directly in living cells. However, the target molecule may be NMR-invisible due to interactions with cellular components, while observing the ligand by 1H NMR is impractical due to the cellular background. Such limitations can be overcome by observing fluorinated ligands by 19F in-cell NMR as they bind to the intracellular target. Here we report a novel approach based on real-time in-cell 19F NMR that allows measuring ligand binding affinities in human cells by competition binding, using a fluorinated compound as a reference. The binding of a set of compounds toward Hsp90α was investigated. In principle, this approach could be applied to other pharmacologically relevant targets, thus aiding the design of more effective compounds in the early stages of drug development.
doi_str_mv 10.1021/acs.jmedchem.3c01600
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10823471</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2918511826</sourcerecordid><originalsourceid>FETCH-LOGICAL-a261t-364c962c0d8d71a5b133cde44caabcca73e000e45302f43de4a2cbe865f3f0ed3</originalsourceid><addsrcrecordid>eNpVkMtOwzAQRS0EoqXwByy8ZJMyfiR1V4gWSpEKSFVZW47ttK4Sp8QJUv8eF7JhNdLM1dHcg9AtgTEBSu6VDuN9ZY3e2WrMNJAM4AwNSUoh4QL4ORoCUJrQjLIBugphDwCMUHaJBkxQkgIVQ_S0clvlTTJTwRo8r6uDbV3rao9nzhvntzg_4rVVZbJxlcVkusDvb2vsPF52lfJ4bssyXKOLQpXB3vRzhD4Xz5v5Mll9vLzOH1eJohlpE5ZxPc2oBiPMhKg0J4xpYznXSuVaqwmz8UXLUwa04CxeFNW5FVlasAKsYSP08Mc9dPmpufVto0p5aFylmqOslZP_L97t5Lb-lgQEZXxCIuGuJzT1V2dDKysXdOygvK27IOmUiJQQQbMYhb9oFC33ddf4WC2S5Mm-_F329mVvn_0A1L55QQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2918511826</pqid></control><display><type>article</type><title>Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Luchinat, Enrico ; Barbieri, Letizia ; Davis, Ben ; Brough, Paul A. ; Pennestri, Matteo ; Banci, Lucia</creator><creatorcontrib>Luchinat, Enrico ; Barbieri, Letizia ; Davis, Ben ; Brough, Paul A. ; Pennestri, Matteo ; Banci, Lucia</creatorcontrib><description>The development of more effective drugs requires knowledge of their bioavailability and binding efficacy directly in the native cellular environment. In-cell nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for investigating ligand–target interactions directly in living cells. However, the target molecule may be NMR-invisible due to interactions with cellular components, while observing the ligand by 1H NMR is impractical due to the cellular background. Such limitations can be overcome by observing fluorinated ligands by 19F in-cell NMR as they bind to the intracellular target. Here we report a novel approach based on real-time in-cell 19F NMR that allows measuring ligand binding affinities in human cells by competition binding, using a fluorinated compound as a reference. The binding of a set of compounds toward Hsp90α was investigated. In principle, this approach could be applied to other pharmacologically relevant targets, thus aiding the design of more effective compounds in the early stages of drug development.</description><identifier>ISSN: 0022-2623</identifier><identifier>ISSN: 1520-4804</identifier><identifier>EISSN: 1520-4804</identifier><identifier>DOI: 10.1021/acs.jmedchem.3c01600</identifier><identifier>PMID: 38215028</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of medicinal chemistry, 2024-01, Vol.67 (2), p.1115-1126</ispartof><rights>2024 The Authors. Published by American Chemical Society</rights><rights>2024 The Authors. Published by American Chemical Society 2024 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-7789-8101 ; 0000-0003-4183-4311 ; 0000-0003-0562-5774</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids></links><search><creatorcontrib>Luchinat, Enrico</creatorcontrib><creatorcontrib>Barbieri, Letizia</creatorcontrib><creatorcontrib>Davis, Ben</creatorcontrib><creatorcontrib>Brough, Paul A.</creatorcontrib><creatorcontrib>Pennestri, Matteo</creatorcontrib><creatorcontrib>Banci, Lucia</creatorcontrib><title>Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells</title><title>Journal of medicinal chemistry</title><addtitle>J. Med. Chem</addtitle><description>The development of more effective drugs requires knowledge of their bioavailability and binding efficacy directly in the native cellular environment. In-cell nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for investigating ligand–target interactions directly in living cells. However, the target molecule may be NMR-invisible due to interactions with cellular components, while observing the ligand by 1H NMR is impractical due to the cellular background. Such limitations can be overcome by observing fluorinated ligands by 19F in-cell NMR as they bind to the intracellular target. Here we report a novel approach based on real-time in-cell 19F NMR that allows measuring ligand binding affinities in human cells by competition binding, using a fluorinated compound as a reference. The binding of a set of compounds toward Hsp90α was investigated. In principle, this approach could be applied to other pharmacologically relevant targets, thus aiding the design of more effective compounds in the early stages of drug development.</description><issn>0022-2623</issn><issn>1520-4804</issn><issn>1520-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVkMtOwzAQRS0EoqXwByy8ZJMyfiR1V4gWSpEKSFVZW47ttK4Sp8QJUv8eF7JhNdLM1dHcg9AtgTEBSu6VDuN9ZY3e2WrMNJAM4AwNSUoh4QL4ORoCUJrQjLIBugphDwCMUHaJBkxQkgIVQ_S0clvlTTJTwRo8r6uDbV3rao9nzhvntzg_4rVVZbJxlcVkusDvb2vsPF52lfJ4bssyXKOLQpXB3vRzhD4Xz5v5Mll9vLzOH1eJohlpE5ZxPc2oBiPMhKg0J4xpYznXSuVaqwmz8UXLUwa04CxeFNW5FVlasAKsYSP08Mc9dPmpufVto0p5aFylmqOslZP_L97t5Lb-lgQEZXxCIuGuJzT1V2dDKysXdOygvK27IOmUiJQQQbMYhb9oFC33ddf4WC2S5Mm-_F329mVvn_0A1L55QQ</recordid><startdate>20240125</startdate><enddate>20240125</enddate><creator>Luchinat, Enrico</creator><creator>Barbieri, Letizia</creator><creator>Davis, Ben</creator><creator>Brough, Paul A.</creator><creator>Pennestri, Matteo</creator><creator>Banci, Lucia</creator><general>American Chemical Society</general><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7789-8101</orcidid><orcidid>https://orcid.org/0000-0003-4183-4311</orcidid><orcidid>https://orcid.org/0000-0003-0562-5774</orcidid></search><sort><creationdate>20240125</creationdate><title>Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells</title><author>Luchinat, Enrico ; Barbieri, Letizia ; Davis, Ben ; Brough, Paul A. ; Pennestri, Matteo ; Banci, Lucia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a261t-364c962c0d8d71a5b133cde44caabcca73e000e45302f43de4a2cbe865f3f0ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luchinat, Enrico</creatorcontrib><creatorcontrib>Barbieri, Letizia</creatorcontrib><creatorcontrib>Davis, Ben</creatorcontrib><creatorcontrib>Brough, Paul A.</creatorcontrib><creatorcontrib>Pennestri, Matteo</creatorcontrib><creatorcontrib>Banci, Lucia</creatorcontrib><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luchinat, Enrico</au><au>Barbieri, Letizia</au><au>Davis, Ben</au><au>Brough, Paul A.</au><au>Pennestri, Matteo</au><au>Banci, Lucia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. Med. Chem</addtitle><date>2024-01-25</date><risdate>2024</risdate><volume>67</volume><issue>2</issue><spage>1115</spage><epage>1126</epage><pages>1115-1126</pages><issn>0022-2623</issn><issn>1520-4804</issn><eissn>1520-4804</eissn><abstract>The development of more effective drugs requires knowledge of their bioavailability and binding efficacy directly in the native cellular environment. In-cell nuclear magnetic resonance (NMR) spectroscopy is a powerful tool for investigating ligand–target interactions directly in living cells. However, the target molecule may be NMR-invisible due to interactions with cellular components, while observing the ligand by 1H NMR is impractical due to the cellular background. Such limitations can be overcome by observing fluorinated ligands by 19F in-cell NMR as they bind to the intracellular target. Here we report a novel approach based on real-time in-cell 19F NMR that allows measuring ligand binding affinities in human cells by competition binding, using a fluorinated compound as a reference. The binding of a set of compounds toward Hsp90α was investigated. In principle, this approach could be applied to other pharmacologically relevant targets, thus aiding the design of more effective compounds in the early stages of drug development.</abstract><pub>American Chemical Society</pub><pmid>38215028</pmid><doi>10.1021/acs.jmedchem.3c01600</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7789-8101</orcidid><orcidid>https://orcid.org/0000-0003-4183-4311</orcidid><orcidid>https://orcid.org/0000-0003-0562-5774</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-2623
ispartof Journal of medicinal chemistry, 2024-01, Vol.67 (2), p.1115-1126
issn 0022-2623
1520-4804
1520-4804
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10823471
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
title Ligand-Based Competition Binding by Real-Time 19F NMR in Human Cells
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T05%3A15%3A50IST&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=Ligand-Based%20Competition%20Binding%20by%20Real-Time%2019F%20NMR%20in%20Human%20Cells&rft.jtitle=Journal%20of%20medicinal%20chemistry&rft.au=Luchinat,%20Enrico&rft.date=2024-01-25&rft.volume=67&rft.issue=2&rft.spage=1115&rft.epage=1126&rft.pages=1115-1126&rft.issn=0022-2623&rft.eissn=1520-4804&rft_id=info:doi/10.1021/acs.jmedchem.3c01600&rft_dat=%3Cproquest_pubme%3E2918511826%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a261t-364c962c0d8d71a5b133cde44caabcca73e000e45302f43de4a2cbe865f3f0ed3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2918511826&rft_id=info:pmid/38215028&rfr_iscdi=true