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        <identifier>oai:www.ideals.illinois.edu:2142/84875</identifier>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Kranz, David M.</dc:contributor>
          <dc:creator>Brodnicki, Thomas Charles</dc:creator>
          <dc:date>2015-09-25T22:28:17Z</dc:date>
          <dc:date>2015-09-25T22:28:17Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1997</dc:date>
          <dc:date>1997</dc:date>
          <dc:description>Mutant 2C scTCRs were further examined in ligand binding experiments. The 2C TCR recognizes a peptide (QL9) presented by the MHC product L$\sp{\rm d}$. Four alanine mutations which affected mAb binding also disrupted binding to the QL9/L$\sp{\rm d}$ complex by greater than ten-fold relative to the wild-type scTCR. A fifth $\alpha$ chain mutation, located within a loop that is analogous to the fourth hypervariable region (HV4) of the $\beta$ chain, disrupted binding to QL9/L$\sp{\rm d}$ approximately five-fold. Based on these results and a homology model of the 2C $\alpha$ chain variable region, these five residues are likely to be involved in either stabilization of CDR loops or in direct contact with the peptide/MHC ligand.</dc:description>
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  Previous issue date: 1997</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 86156
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>195 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1997.</dc:description>
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          <dc:identifier>(MiAaPQ)AAI9717257</dc:identifier>
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          <dc:subject>Health Sciences, Immunology</dc:subject>
          <dc:title>T Cell Receptor Alpha Chain Residues Involved in Antibody Binding and Recognition of peptide/MHC Ligand</dc:title>
          <dc:type>text</dc:type>
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            <grantor>University of Illinois at Urbana-Champaign</grantor>
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            <name>Ph.D.</name>
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