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dc.contributor.advisorAndrade, Rodrigo
dc.contributor.authorOuellette, Andrea
dc.date.accessioned2011-10-18T12:46:14Z
dc.date.available2011-10-18T12:46:14Z
dc.date.issued2002
dc.identifier.urihttp://hdl.handle.net/10920/23649
dc.descriptionvii, 29 p.en_US
dc.description.abstractAs many as 20 mammalian homologues to the Drosophila melanogaster transient receptor potential (TRP) gene have been identified and, along with others in the Cenhabordis elegans genome, constitute the TRP gene family. Despite continuous and careful research for the past two decades, the mechanism by which the TRP family of ion channels is activated has evaded scientists. Intracellular Ca2+ store depletion is one hypothesis for the gating of TRP channels, and some researchers believe that TRP is responsible for the calcium-release-activated current, Icrac. Although TRP proteins were first thought to assemble as homomeric cation channels, it has been shown that different TRP proteins coassemble to form functional cation channels. To determine the electrophysiological properties of TRP channels, we expressed human TRP1 and urine TRP4 in human embryonic kidney cells. Co-expression of TRP1 and TRP4 also revealed that TRP4 is an integral part of the resulting channels, and we confirmed that cationic currents can be carried by such heteromers. Further recordings revealed that the arrangement of TRP subunits in the channel tetramer might be responsible for the voltage-dependence/independence of Ca2+ currents detected by voltage clamp technique. In addition, we demonstrate by comparison of the TRP1/4 current-voltage relationship with that of Icrac that the heteromer TRP1/4 is not responsible for Icrac. Although TRP1/4 channels are not responsible for the endogenous Icrac, the electrophysiological recordings in this study show that TRP channels may be responsible for endogenous currents recorded from the pyramidal cells of the prefrontal cortex of rats.en_US
dc.description.sponsorshipDepartment of Psychiatry and Behavioral Neuroscience. School of Medicine. Wayne State University. Detroit, Michigan.
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleVoltage Dependence of the Cation-Nonselective TRP Channels Expressed in HEK293 Cellsen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


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  • Biology Senior Individualized Projects [1489]
    This collection includes Senior Individualized Projects (SIP's) completed in the Biology Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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