{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/108239"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/108239","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Development of chemical tools for studying biology with light: Photoactivatable donors and photoacoustic probes","abstract":"Chemical tools are essential for the study of complex biological processes. Generally, this is achieved through the controlled perturbation of a biological system and the observation of an effect. In this work, we present the development of molecular tools for both of these aspects. The first chapter highlights our rational development of a photo-controlled formaldehyde do-nor with an internal fluorescence response upon activation. This tool enabled us to establish an assay for the quantification of the released reactive carbon species into the intracellular space. Using this unique approach, we evaluated the dose-dependent impairment of HEK293 cells by formaldehyde in a wound healing assay and showed the potential cytotoxicity of common formaldehyde-releasing prodrug approaches. The second and third chapter summarize our ap-proaches towards activatable contrast agents for photoacoustic imaging, an emerging deep-tissue imaging modality. To address a lack of modular activatable probes for this imaging technique, we combined the analyte specificity of DNA aptamers with commercially available fluorophores to show the feasibility of a general approach. For our proof-of-concept study, we used a thrombin-selective aptamer and were able to show a selective modulation of the photo-acoustic signal upon exposure to thrombin in vitro and in vivo. In addition, we are currently developing new dye platforms, imaging techniques and probes for photoacoustic imaging.","abstract_html":"Chemical tools are essential for the study of complex biological processes. Generally, this is achieved through the controlled perturbation of a biological system and the observation of an effect. In this work, we present the development of molecular tools for both of these aspects. The first chapter highlights our rational development of a photo-controlled formaldehyde do-nor with an internal fluorescence response upon activation. This tool enabled us to establish an assay for the quantification of the released reactive carbon species into the intracellular space. Using this unique approach, we evaluated the dose-dependent impairment of HEK293 cells by formaldehyde in a wound healing assay and showed the potential cytotoxicity of common formaldehyde-releasing prodrug approaches. The second and third chapter summarize our ap-proaches towards activatable contrast agents for photoacoustic imaging, an emerging deep-tissue imaging modality. To address a lack of modular activatable probes for this imaging technique, we combined the analyte specificity of DNA aptamers with commercially available fluorophores to show the feasibility of a general approach. For our proof-of-concept study, we used a thrombin-selective aptamer and were able to show a selective modulation of the photo-acoustic signal upon exposure to thrombin in vitro and in vivo. In addition, we are currently developing new dye platforms, imaging techniques and probes for photoacoustic imaging.","abstract_has_math":false,"creators":["Smaga, Lukas P."],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Chan, Jefferson","Mitchell, Douglas A","Sarlah, David","Zimmerman, Steven C"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2020,"date_issued":"2020-08-27T00:49:52Z","date_published":"2020-08-27T00:49:52Z","updated_at":"2026-07-22T22:24:48Z","subjects":["Formaldehyde, Photoacoustic Imaging"],"languages":["en"],"rights":["Copyright 2020 Lukas P. 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Using this unique approach, we evaluated the dose-dependent impairment of HEK293 cells by formaldehyde in a wound healing assay and showed the potential cytotoxicity of common formaldehyde-releasing prodrug approaches. The second and third chapter summarize our ap-proaches towards activatable contrast agents for photoacoustic imaging, an emerging deep-tissue imaging modality. To address a lack of modular activatable probes for this imaging technique, we combined the analyte specificity of DNA aptamers with commercially available fluorophores to show the feasibility of a general approach. For our proof-of-concept study, we used a thrombin-selective aptamer and were able to show a selective modulation of the photo-acoustic signal upon exposure to thrombin in vitro and in vivo. In addition, we are currently developing new dye platforms, imaging techniques and probes for photoacoustic imaging.","Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2022-05-01","The student, Lukas Smaga, accepted the attached license on 2020-04-01 at 04:40.","The student, Lukas Smaga, submitted this Dissertation for approval on 2020-04-01 at 05:04.","This Dissertation was approved for publication on 2020-04-09 at 08:49.","DSpace SAF Submission Ingestion Package generated from Vireo submission #14929 on 2020-08-25 at 17:39:47","Made available in DSpace on 2020-08-27T00:49:52Z (GMT). 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Generally, this is achieved through the controlled perturbation of a biological system and the observation of an effect. In this work, we present the development of molecular tools for both of these aspects. The first chapter highlights our rational development of a photo-controlled formaldehyde do-nor with an internal fluorescence response upon activation. This tool enabled us to establish an assay for the quantification of the released reactive carbon species into the intracellular space. Using this unique approach, we evaluated the dose-dependent impairment of HEK293 cells by formaldehyde in a wound healing assay and showed the potential cytotoxicity of common formaldehyde-releasing prodrug approaches. The second and third chapter summarize our ap-proaches towards activatable contrast agents for photoacoustic imaging, an emerging deep-tissue imaging modality. To address a lack of modular activatable probes for this imaging technique, we combined the analyte specificity of DNA aptamers with commercially available fluorophores to show the feasibility of a general approach. For our proof-of-concept study, we used a thrombin-selective aptamer and were able to show a selective modulation of the photo-acoustic signal upon exposure to thrombin in vitro and in vivo. 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