Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI
In the past decade, it has become possible to use the nuclear (proton, 1 H) signal of the hydrogen atoms in water for noninvasive assessment of functional and physiological parameters with magnetic resonance imaging (MRI). Here we show that it is possible to produce pH-sensitive MRI contrast by expl...
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Veröffentlicht in: | Nature medicine 2003-08, Vol.9 (8), p.1085-1090 |
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description | In the past decade, it has become possible to use the nuclear (proton,
1
H) signal of the hydrogen atoms in water for noninvasive assessment of functional and physiological parameters with magnetic resonance imaging (MRI). Here we show that it is possible to produce pH-sensitive MRI contrast by exploiting the exchange between the hydrogen atoms of water and the amide hydrogen atoms of endogenous mobile cellular proteins and peptides. Although amide proton concentrations are in the millimolar range, we achieved a detection sensitivity of several percent on the water signal (molar concentration). The pH dependence of the signal was calibrated
in situ
, using phosphorus spectroscopy to determine pH, and proton exchange spectroscopy to measure the amide proton transfer rate. To show the potential of amide proton transfer (APT) contrast for detecting acute stroke, pH effects were noninvasively imaged in ischemic rat brain. This observation opens the possibility of using intrinsic pH contrast, as well as protein- and/or peptide-content contrast, as diagnostic tools in clinical imaging. |
doi_str_mv | 10.1038/nm907 |
format | Article |
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1
H) signal of the hydrogen atoms in water for noninvasive assessment of functional and physiological parameters with magnetic resonance imaging (MRI). Here we show that it is possible to produce pH-sensitive MRI contrast by exploiting the exchange between the hydrogen atoms of water and the amide hydrogen atoms of endogenous mobile cellular proteins and peptides. Although amide proton concentrations are in the millimolar range, we achieved a detection sensitivity of several percent on the water signal (molar concentration). The pH dependence of the signal was calibrated
in situ
, using phosphorus spectroscopy to determine pH, and proton exchange spectroscopy to measure the amide proton transfer rate. To show the potential of amide proton transfer (APT) contrast for detecting acute stroke, pH effects were noninvasively imaged in ischemic rat brain. This observation opens the possibility of using intrinsic pH contrast, as well as protein- and/or peptide-content contrast, as diagnostic tools in clinical imaging.</description><identifier>ISSN: 1078-8956</identifier><identifier>EISSN: 1546-170X</identifier><identifier>DOI: 10.1038/nm907</identifier><identifier>PMID: 12872167</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Brain - anatomy & histology ; Cancer Research ; Hydrogen ; Hydrogen-Ion Concentration ; Infectious Diseases ; Ischemia - metabolism ; Magnetic Resonance Imaging - methods ; Metabolic Diseases ; Molecular Medicine ; Neurosciences ; Peptides ; Peptides - chemistry ; Physiology ; Proteins - chemistry ; Protons ; Rats ; Rats, Sprague-Dawley ; Spectroscopy ; technical-report ; Water - chemistry</subject><ispartof>Nature medicine, 2003-08, Vol.9 (8), p.1085-1090</ispartof><rights>Springer Nature America, Inc. 2003</rights><rights>COPYRIGHT 2003 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Aug 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c624t-51c3fa9eb7a8298e662c535de17c9a7fe7e109af0446b1f32a3b98f40ec4cd53</citedby><cites>FETCH-LOGICAL-c624t-51c3fa9eb7a8298e662c535de17c9a7fe7e109af0446b1f32a3b98f40ec4cd53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2727,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12872167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Jinyuan</creatorcontrib><creatorcontrib>van Zijl, Peter C M</creatorcontrib><creatorcontrib>Payen, Jean-Francois</creatorcontrib><creatorcontrib>Wilson, David A</creatorcontrib><creatorcontrib>Traystman, Richard J</creatorcontrib><title>Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><addtitle>Nat Med</addtitle><description>In the past decade, it has become possible to use the nuclear (proton,
1
H) signal of the hydrogen atoms in water for noninvasive assessment of functional and physiological parameters with magnetic resonance imaging (MRI). Here we show that it is possible to produce pH-sensitive MRI contrast by exploiting the exchange between the hydrogen atoms of water and the amide hydrogen atoms of endogenous mobile cellular proteins and peptides. Although amide proton concentrations are in the millimolar range, we achieved a detection sensitivity of several percent on the water signal (molar concentration). The pH dependence of the signal was calibrated
in situ
, using phosphorus spectroscopy to determine pH, and proton exchange spectroscopy to measure the amide proton transfer rate. To show the potential of amide proton transfer (APT) contrast for detecting acute stroke, pH effects were noninvasively imaged in ischemic rat brain. This observation opens the possibility of using intrinsic pH contrast, as well as protein- and/or peptide-content contrast, as diagnostic tools in clinical imaging.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain - anatomy & histology</subject><subject>Cancer Research</subject><subject>Hydrogen</subject><subject>Hydrogen-Ion Concentration</subject><subject>Infectious Diseases</subject><subject>Ischemia - metabolism</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Metabolic Diseases</subject><subject>Molecular Medicine</subject><subject>Neurosciences</subject><subject>Peptides</subject><subject>Peptides - chemistry</subject><subject>Physiology</subject><subject>Proteins - chemistry</subject><subject>Protons</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Spectroscopy</subject><subject>technical-report</subject><subject>Water - chemistry</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNktFr1TAUxosobs79BYIEwYEPnUmTNs3jGOouTAZzim8lNz3pzWiTmqTg_vul68XrHQMlDwk5v-87h4-TZccEnxJM6492EJg_yw5JyaqccPzzeXpjXue1KKuD7FUItxhjikvxMjsgRc0LUvHDTH4PxnYobgDJwbSARu-isyiYzso-IKeRsdFLBX0_9dI_1MHYgKRt0QhjTKKAokMtRFARjRcItE6vkITo6_XqdfZCJyc43t5H2c3nTzfnF_nl1ZfV-dllrqqCxbwkimopYM1lXYgaqqpQJS1bIFwJyTVwIFhIjRmr1kTTQtK1qDXDoJhqS3qUnSy2acBfE4TYDCbMU0sLbgoNpyUVtPg3SATjjOMZfPcIvHWTn1NpioISQhlhCcoXqJM9NMZqN4fVgQUve2dBm_R9RlLnGhe4SvzpE3w6LQxGPSn4sCdITITfsZNTCM3q2_X_s1c_9tmTv9gNyD5uguunaJwN--D7BVTeheBBN6M3g_R3DcHNvHrNw-ol7u02rmk9QLujtru26xhSyXbgd3k-dnqzgFbGycMfp6V6D5gd5gQ</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Zhou, Jinyuan</creator><creator>van Zijl, Peter C M</creator><creator>Payen, Jean-Francois</creator><creator>Wilson, David A</creator><creator>Traystman, Richard J</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20030801</creationdate><title>Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI</title><author>Zhou, Jinyuan ; van Zijl, Peter C M ; Payen, Jean-Francois ; Wilson, David A ; Traystman, Richard J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c624t-51c3fa9eb7a8298e662c535de17c9a7fe7e109af0446b1f32a3b98f40ec4cd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain - anatomy & histology</topic><topic>Cancer Research</topic><topic>Hydrogen</topic><topic>Hydrogen-Ion Concentration</topic><topic>Infectious Diseases</topic><topic>Ischemia - metabolism</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Metabolic Diseases</topic><topic>Molecular Medicine</topic><topic>Neurosciences</topic><topic>Peptides</topic><topic>Peptides - chemistry</topic><topic>Physiology</topic><topic>Proteins - chemistry</topic><topic>Protons</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Spectroscopy</topic><topic>technical-report</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Jinyuan</creatorcontrib><creatorcontrib>van Zijl, Peter C M</creatorcontrib><creatorcontrib>Payen, Jean-Francois</creatorcontrib><creatorcontrib>Wilson, David A</creatorcontrib><creatorcontrib>Traystman, Richard 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>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>Proquest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Jinyuan</au><au>van Zijl, Peter C M</au><au>Payen, Jean-Francois</au><au>Wilson, David A</au><au>Traystman, Richard J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI</atitle><jtitle>Nature medicine</jtitle><stitle>Nat Med</stitle><addtitle>Nat Med</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>9</volume><issue>8</issue><spage>1085</spage><epage>1090</epage><pages>1085-1090</pages><issn>1078-8956</issn><eissn>1546-170X</eissn><abstract>In the past decade, it has become possible to use the nuclear (proton,
1
H) signal of the hydrogen atoms in water for noninvasive assessment of functional and physiological parameters with magnetic resonance imaging (MRI). Here we show that it is possible to produce pH-sensitive MRI contrast by exploiting the exchange between the hydrogen atoms of water and the amide hydrogen atoms of endogenous mobile cellular proteins and peptides. Although amide proton concentrations are in the millimolar range, we achieved a detection sensitivity of several percent on the water signal (molar concentration). The pH dependence of the signal was calibrated
in situ
, using phosphorus spectroscopy to determine pH, and proton exchange spectroscopy to measure the amide proton transfer rate. To show the potential of amide proton transfer (APT) contrast for detecting acute stroke, pH effects were noninvasively imaged in ischemic rat brain. This observation opens the possibility of using intrinsic pH contrast, as well as protein- and/or peptide-content contrast, as diagnostic tools in clinical imaging.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>12872167</pmid><doi>10.1038/nm907</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Brain - anatomy & histology Cancer Research Hydrogen Hydrogen-Ion Concentration Infectious Diseases Ischemia - metabolism Magnetic Resonance Imaging - methods Metabolic Diseases Molecular Medicine Neurosciences Peptides Peptides - chemistry Physiology Proteins - chemistry Protons Rats Rats, Sprague-Dawley Spectroscopy technical-report Water - chemistry |
title | Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI |
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