Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties

A new synthetic methodology for the combinatorial preparation of C-terminus-modified Green and Red Fluorescent Protein chromophores is described. This method involves the modification of the previously reported [2+3] cycloaddition reaction scheme to incorporate new R2 groups in the imidate used in t...

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Main Author: Fellows, William Brett
Other Authors: Tolbert, Laren M.
Format: Others
Language:en_US
Published: Georgia Institute of Technology 2014
Subjects:
Online Access:http://hdl.handle.net/1853/52318
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spelling ndltd-GATECH-oai-smartech.gatech.edu-1853-523182014-09-13T03:33:56ZCombinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical propertiesFellows, William BrettGreen fluorescent proteinChromophoreSynthesisCombinatorialRed fluorescent proteinHot dog stackingSolid stateCrystal structureAggregate induced emissionReprecipitationA new synthetic methodology for the combinatorial preparation of C-terminus-modified Green and Red Fluorescent Protein chromophores is described. This method involves the modification of the previously reported [2+3] cycloaddition reaction scheme to incorporate new R2 groups in the imidate used in the final step. This is achieved through two primary routes: (a) the imidation of nitriles using hydrochloric acid gas and (b) the O-alkylation of amides using a variant of Meerwein's Salt to provide conjugated imidates. The preparation of fluorescent microcrystals and nanofibers from Green Fluorescent Protein chromophore derivatives via the reprecipitation method is also demonstrated. The properties of these microcrystals and nanofibers, especially in relation to the powder obtained from organic solvents, are also explored. Additionally, it is demonstrated that the size and shape of the microcrystals and nanofibers can be modulated with varying experimental conditions for RP. A new class of AIE-active GFP chromophores is reported. These chromophores contain a benzoxazole group on the phenyl ring and varying lengths of alkyl chains on the imidazolidinone nitrogen. These benzoxazole-based chromophores exhibit unique properties in the solid state not previously observed for GFP chromophore derivatives, namely, a broadening of the excitation spectrum and red-shifting of the emission, likely caused by excimer formation. The crystal structure also reveals a unique "hot-dog" stacking motif. Additionally, some projects which require further work are discussed at the end of the thesis. These include a stress-responsive GFP-based polymer and DNA-binding fluorophores.Georgia Institute of TechnologyTolbert, Laren M.2014-08-27T13:41:33Z2014-08-27T13:41:33Z2014-082014-07-03August 20142014-08-27T13:41:33ZDissertationapplication/pdfhttp://hdl.handle.net/1853/52318en_US
collection NDLTD
language en_US
format Others
sources NDLTD
topic Green fluorescent protein
Chromophore
Synthesis
Combinatorial
Red fluorescent protein
Hot dog stacking
Solid state
Crystal structure
Aggregate induced emission
Reprecipitation
spellingShingle Green fluorescent protein
Chromophore
Synthesis
Combinatorial
Red fluorescent protein
Hot dog stacking
Solid state
Crystal structure
Aggregate induced emission
Reprecipitation
Fellows, William Brett
Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties
description A new synthetic methodology for the combinatorial preparation of C-terminus-modified Green and Red Fluorescent Protein chromophores is described. This method involves the modification of the previously reported [2+3] cycloaddition reaction scheme to incorporate new R2 groups in the imidate used in the final step. This is achieved through two primary routes: (a) the imidation of nitriles using hydrochloric acid gas and (b) the O-alkylation of amides using a variant of Meerwein's Salt to provide conjugated imidates. The preparation of fluorescent microcrystals and nanofibers from Green Fluorescent Protein chromophore derivatives via the reprecipitation method is also demonstrated. The properties of these microcrystals and nanofibers, especially in relation to the powder obtained from organic solvents, are also explored. Additionally, it is demonstrated that the size and shape of the microcrystals and nanofibers can be modulated with varying experimental conditions for RP. A new class of AIE-active GFP chromophores is reported. These chromophores contain a benzoxazole group on the phenyl ring and varying lengths of alkyl chains on the imidazolidinone nitrogen. These benzoxazole-based chromophores exhibit unique properties in the solid state not previously observed for GFP chromophore derivatives, namely, a broadening of the excitation spectrum and red-shifting of the emission, likely caused by excimer formation. The crystal structure also reveals a unique "hot-dog" stacking motif. Additionally, some projects which require further work are discussed at the end of the thesis. These include a stress-responsive GFP-based polymer and DNA-binding fluorophores.
author2 Tolbert, Laren M.
author_facet Tolbert, Laren M.
Fellows, William Brett
author Fellows, William Brett
author_sort Fellows, William Brett
title Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties
title_short Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties
title_full Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties
title_fullStr Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties
title_full_unstemmed Combinatorial synthesis of new GFP- and RFP-like chromophores and their photophysical properties
title_sort combinatorial synthesis of new gfp- and rfp-like chromophores and their photophysical properties
publisher Georgia Institute of Technology
publishDate 2014
url http://hdl.handle.net/1853/52318
work_keys_str_mv AT fellowswilliambrett combinatorialsynthesisofnewgfpandrfplikechromophoresandtheirphotophysicalproperties
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