{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/85426"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/85426","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Two -Photon Dual Channel Fluctuation Correlation Spectroscopy: Theory and Application","abstract":"Fluctuation correlation spectroscopy (FCS) is a non-perturbative method used to gain molecular information from stochastic processes such as Brownian motion (Magde, Elson et al. 1972). Dual channel FCS allows for the investigation of static (molecular associations) and kinetic (protein dynamics) parameters of interaction between two species. This technique is able to quantitate in vivo molecular interactions that are critical for cellular study. Data acquisition hardware was built which allows 25 ns time resolution and records the entire photon sequence using a hardware data compression technique. This allows multiple analysis to be performed (i.e. photon counting histogram (Muller, Chen et al. 1999), moment analysis, etc.) The basic theory and simulation of oligomer size effect on dual channel FCS data was done to allow interpretation of an in vivo study involving the amount of aggregation between different somatostatin membrane receptors. The cross-correlation, in combination with Forster resonance energy transfer (FRET), provides a more elegant method to study protein dynamics than the equivalent quenching experiment involving only one channel of detection (Haas and Steinberg 1984). The extra relaxation is present as an extra hump in the autocorrelation and as an anti-correlation for the cross-correlation. This signature anti-correlation differentiates this process from others such as triplet state, rotational diffusion, quenching, etc. In vitro confirmation is provided through studies of ribosome and cameleon proteins.","abstract_html":"Fluctuation correlation spectroscopy (FCS) is a non-perturbative method used to gain molecular information from stochastic processes such as Brownian motion (Magde, Elson et al. 1972). Dual channel FCS allows for the investigation of static (molecular associations) and kinetic (protein dynamics) parameters of interaction between two species. This technique is able to quantitate in vivo molecular interactions that are critical for cellular study. Data acquisition hardware was built which allows 25 ns time resolution and records the entire photon sequence using a hardware data compression technique. This allows multiple analysis to be performed (i.e. photon counting histogram (Muller, Chen et al. 1999), moment analysis, etc.) The basic theory and simulation of oligomer size effect on dual channel FCS data was done to allow interpretation of an in vivo study involving the amount of aggregation between different somatostatin membrane receptors. The cross-correlation, in combination with Forster resonance energy transfer (FRET), provides a more elegant method to study protein dynamics than the equivalent quenching experiment involving only one channel of detection (Haas and Steinberg 1984). The extra relaxation is present as an extra hump in the autocorrelation and as an anti-correlation for the cross-correlation. This signature anti-correlation differentiates this process from others such as triplet state, rotational diffusion, quenching, etc. In vitro confirmation is provided through studies of ribosome and cameleon proteins.","abstract_has_math":false,"creators":["Eid, John Safwat"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Biophysics and Computational Biology","degree_department":null,"school":null,"contributors":["Gratton, Enrico"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-09-25T22:46:03Z","date_published":"2015-09-25T22:46:03Z","updated_at":"2026-07-22T22:26:25Z","subjects":["Biophysics, General"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(MiAaPQ)AAI3069990"],"render_values":[{"text":"(MiAaPQ)AAI3069990","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/85426","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Gratton, Enrico"]},{"key":"dc:creator","label":"Author","values":["Eid, John Safwat"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2015-09-25T22:46:03Z","10000-01-01","2002"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biophysics and Computational Biology"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biophysics, General"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/85426","(MiAaPQ)AAI3069990"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Fluctuation correlation spectroscopy (FCS) is a non-perturbative method used to gain molecular information from stochastic processes such as Brownian motion (Magde, Elson et al. 1972). Dual channel FCS allows for the investigation of static (molecular associations) and kinetic (protein dynamics) parameters of interaction between two species. This technique is able to quantitate in vivo molecular interactions that are critical for cellular study. Data acquisition hardware was built which allows 25 ns time resolution and records the entire photon sequence using a hardware data compression technique. This allows multiple analysis to be performed (i.e. photon counting histogram (Muller, Chen et al. 1999), moment analysis, etc.) The basic theory and simulation of oligomer size effect on dual channel FCS data was done to allow interpretation of an in vivo study involving the amount of aggregation between different somatostatin membrane receptors. The cross-correlation, in combination with Forster resonance energy transfer (FRET), provides a more elegant method to study protein dynamics than the equivalent quenching experiment involving only one channel of detection (Haas and Steinberg 1984). The extra relaxation is present as an extra hump in the autocorrelation and as an anti-correlation for the cross-correlation. This signature anti-correlation differentiates this process from others such as triplet state, rotational diffusion, quenching, etc. In vitro confirmation is provided through studies of ribosome and cameleon proteins.","Made available in DSpace on 2015-09-25T22:46:03Z (GMT). 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Dual channel FCS allows for the investigation of static (molecular associations) and kinetic (protein dynamics) parameters of interaction between two species. This technique is able to quantitate in vivo molecular interactions that are critical for cellular study. Data acquisition hardware was built which allows 25 ns time resolution and records the entire photon sequence using a hardware data compression technique. This allows multiple analysis to be performed (i.e. photon counting histogram (Muller, Chen et al. 1999), moment analysis, etc.) The basic theory and simulation of oligomer size effect on dual channel FCS data was done to allow interpretation of an in vivo study involving the amount of aggregation between different somatostatin membrane receptors. The cross-correlation, in combination with Forster resonance energy transfer (FRET), provides a more elegant method to study protein dynamics than the equivalent quenching experiment involving only one channel of detection (Haas and Steinberg 1984). The extra relaxation is present as an extra hump in the autocorrelation and as an anti-correlation for the cross-correlation. This signature anti-correlation differentiates this process from others such as triplet state, rotational diffusion, quenching, etc. In vitro confirmation is provided through studies of ribosome and cameleon proteins.","Made available in DSpace on 2015-09-25T22:46:03Z (GMT). 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