<?xml version='1.0' encoding='UTF-8'?><?xml-stylesheet href='static/style.xsl' type='text/xsl'?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-19T17:28:31Z</responseDate><request verb="GetRecord" identifier="oai:ecommons.cornell.edu:1813/67559" metadataPrefix="dim">https://ecommons.cornell.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:ecommons.cornell.edu:1813/67559</identifier><datestamp>2026-05-15T19:47:10Z</datestamp><setSpec>com_1813_35</setSpec><setSpec>col_1813_47</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author">Walker, Joshua Aaron</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="chair">Alabi, Christopher Akinleye</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="committeeMember">Delisa, Matthew</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="committeeMember">Baird, Barbara Ann</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2019-10-15T16:48:09Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2020-08-29T06:00:21Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2019-08-30</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="other">ProQuest Submission ID: 11591</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="other">ProQuest Publication ID: 22587779</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1813/67559</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="doi">https://doi.org/10.7298/vzs9-0176</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="bibid">11050542</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">Bioconjugates are an indispensable tool for molecular biology as well as an established modality for biomedical imaging and drug delivery. Broadly, bioconjugation is the use of a chemical cross-linker to covalently attach non-natural reporters, chemical handles, drug cargo, or targeting ligands to biologics to augment their innate properties and functions. Many bioconjugation strategies attach a single non-natural component to the biomolecule of interest. This limits the functional complexity of the resulting bioconjugate. Incorporating multiple functionalities and/or stimuli responsive units has the potential to enable new applications of bioconjugates as molecular probes and drug carriers. Herein, we present a survey of our work towards developing multifunctional bioconjugates. We develop a new strategy for the site-specific modification of native antibodies. This strategy enables dual “click” modification of native antibodies. We also develop new synthetic methods for the synthesis of oligothioetheramides. We apply this new synthesis to study the effect of cross-linker sequence on the biophysical properties of antibody-drug conjugates. Finally, we discuss our efforts to develop molecular probes to characterize the surface of extracellular vesicles and quantify endosomal escape for siRNA therapeutics. Taken together, these works highlight the importance of chemical cross-linkers in the design of multifunctional bioconjugates for a variety of applications.</dim:field>
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   <dim:field mdschema="dc" element="subject">Chemical engineering</dim:field>
   <dim:field mdschema="dc" element="subject">Antibody-drug Conjugates</dim:field>
   <dim:field mdschema="dc" element="subject">Bioconjugates</dim:field>
   <dim:field mdschema="dc" element="subject">Click Chemistry</dim:field>
   <dim:field mdschema="dc" element="subject">Sequence-defined Polymers</dim:field>
   <dim:field mdschema="dc" element="subject">siRNA Therapeutics</dim:field>
   <dim:field mdschema="dc" element="subject">Site-specific Protein Modification</dim:field>
   <dim:field mdschema="dc" element="subject">Chemistry</dim:field>
   <dim:field mdschema="dc" element="subject">Bioengineering</dim:field>
   <dim:field mdschema="dc" element="title">Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes</dim:field>
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   <dim:field mdschema="thesis" element="degree" qualifier="discipline">Chemical Engineering</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="grantor">Cornell University</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="level">Doctor of Philosophy</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="name">Ph.D., Chemical Engineering</dim:field>
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   <dim:field mdschema="cris" element="virtual" qualifier="author">Walker, Joshua Aaron</dim:field>
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   	&lt;Title>Multifunctional Chemical Cross-linkers for Drug Carriers and Molecular Probes&lt;/Title>
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   	&lt;PublicationDate>2019-08-30&lt;/PublicationDate>
   	&lt;DOI>https://doi.org/10.7298/vzs9-0176&lt;/DOI>
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        	&lt;DisplayName>Walker, Joshua Aaron&lt;/DisplayName>
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    &lt;Keyword>Chemical engineering&lt;/Keyword>
    &lt;Keyword>Antibody-drug Conjugates&lt;/Keyword>
    &lt;Keyword>Bioconjugates&lt;/Keyword>
    &lt;Keyword>Click Chemistry&lt;/Keyword>
    &lt;Keyword>Sequence-defined Polymers&lt;/Keyword>
    &lt;Keyword>siRNA Therapeutics&lt;/Keyword>
    &lt;Keyword>Site-specific Protein Modification&lt;/Keyword>
    &lt;Keyword>Chemistry&lt;/Keyword>
    &lt;Keyword>Bioengineering&lt;/Keyword>
   	&lt;Abstract>Bioconjugates are an indispensable tool for molecular biology as well as an established modality for biomedical imaging and drug delivery. Broadly, bioconjugation is the use of a chemical cross-linker to covalently attach non-natural reporters, chemical handles, drug cargo, or targeting ligands to biologics to augment their innate properties and functions. Many bioconjugation strategies attach a single non-natural component to the biomolecule of interest. This limits the functional complexity of the resulting bioconjugate. Incorporating multiple functionalities and/or stimuli responsive units has the potential to enable new applications of bioconjugates as molecular probes and drug carriers. Herein, we present a survey of our work towards developing multifunctional bioconjugates. We develop a new strategy for the site-specific modification of native antibodies. This strategy enables dual “click” modification of native antibodies. We also develop new synthetic methods for the synthesis of oligothioetheramides. We apply this new synthesis to study the effect of cross-linker sequence on the biophysical properties of antibody-drug conjugates. Finally, we discuss our efforts to develop molecular probes to characterize the surface of extracellular vesicles and quantify endosomal escape for siRNA therapeutics. Taken together, these works highlight the importance of chemical cross-linkers in the design of multifunctional bioconjugates for a variety of applications.&lt;/Abstract>
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