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dc.contributor.authorZhang, Lejie
dc.contributor.authorZhang, Mei
dc.contributor.authorBellve, Karl D.
dc.contributor.authorFogarty, Kevin E.
dc.contributor.authorCastro, Maite A.
dc.contributor.authorBrauchi, Sebastian
dc.contributor.authorKobertz, William R.
dc.date2022-08-11T08:08:24.000
dc.date.accessioned2022-08-23T15:53:59Z
dc.date.available2022-08-23T15:53:59Z
dc.date.issued2019-09-25
dc.date.submitted2020-06-01
dc.identifier.citation<p>bioRxiv 781799; doi: https://doi.org/10.1101/781799. <a href="https://doi.org/10.1101/781799" target="_blank">Link to preprint on bioRxiv service.</a></p>
dc.identifier.doi10.1101/781799
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29461
dc.description.abstractSmall molecule fluorescent wheat germ agglutinin (WGA) conjugates are routinely used to demarcate mammalian plasma membranes because they bind to the cell’s glycocalyx. Here we describe the derivatization of WGA with a pH sensitive rhodamine fluorophore (pHRho: pKa = 7) to detect proton channel fluxes and extracellular proton accumulation and depletion from primary cells. We found that WGA-pHRho labeling was uniform, did not appreciably alter the voltage-gating of glycosylated ion channels, and the extracellular changes in pH directly correlated with proton channel activity. Using single plane illumination techniques, WGA-pHRho was used to detect spatiotemporal differences in proton accumulation and depletion over the extracellular surface of cardiomyocytes, astrocytes, and neurons. Because WGA can be derivatized with any small molecule fluorescent ion sensor, WGA conjugates should prove useful to visualize most electrogenic and non-electrogenic events on the extracellular side of the plasma membrane.
dc.language.isoen_US
dc.relation<p>Now published in <em>The Journal of General Physiology</em> doi: <a href="http://dx.doi.org/10.1085/jgp.201912498" target="_blank">10.1085/jgp.201912498</a></p>
dc.rightsThe copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC-ND 4.0 International license.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectwheat germ agglutinin
dc.subjectproton channel fluxes
dc.subjectplasma membranes
dc.subjectbiophysics
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectBiochemistry
dc.subjectBiophysics
dc.titleWheat Germ Agglutinin Conjugated Fluorescent pH Sensors for Visualizing Proton Fluxes [preprint]
dc.typePreprint
dc.source.journaltitlebioRxiv
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2705&amp;context=faculty_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1686
dc.identifier.contextkey17935224
refterms.dateFOA2022-08-23T15:53:59Z
html.description.abstract<p><p id="x-x-x-p-2">Small molecule fluorescent wheat germ agglutinin (WGA) conjugates are routinely used to demarcate mammalian plasma membranes because they bind to the cell’s glycocalyx. Here we describe the derivatization of WGA with a pH sensitive rhodamine fluorophore (pHRho: pKa = 7) to detect proton channel fluxes and extracellular proton accumulation and depletion from primary cells. We found that WGA-pHRho labeling was uniform, did not appreciably alter the voltage-gating of glycosylated ion channels, and the extracellular changes in pH directly correlated with proton channel activity. Using single plane illumination techniques, WGA-pHRho was used to detect spatiotemporal differences in proton accumulation and depletion over the extracellular surface of cardiomyocytes, astrocytes, and neurons. Because WGA can be derivatized with any small molecule fluorescent ion sensor, WGA conjugates should prove useful to visualize most electrogenic and non-electrogenic events on the extracellular side of the plasma membrane.</p>
dc.identifier.submissionpathfaculty_pubs/1686
dc.contributor.departmentBiomedical Imaging Group, Program in Molecular Medicine
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology


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The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC-ND 4.0 International license.
Except where otherwise noted, this item's license is described as The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC-ND 4.0 International license.