THESIS
2015
ii leaves, iii-xxxvi, 177 pages : illustrations (some color) ; 30 cm
Abstract
Fluorescence-based techniques are powerful tools for bioscience and biotechnology
research. They are often considered as probes for quantifying and qualifying
biomolecules and visualizers for real-time tracking of biological events. In conventional
fluorescent systems, their strong fluorescence in dilute solutions will be weakened or quenched when their molecules are aggregated in poor solvents or they are fabricated as
solid their films. Such "aggregation-caused quenching" (ACQ) effect has greatly limited
their scope for high-technological applications.
In 2001, an opposite phenomenon to ACQ called "aggregation-induced emission"
(AIE) was discovered. Luminogens with AIE characteristics are generally
non-luminescent in solutions but emit intensely in the aggregated state. They...[
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Fluorescence-based techniques are powerful tools for bioscience and biotechnology
research. They are often considered as probes for quantifying and qualifying
biomolecules and visualizers for real-time tracking of biological events. In conventional
fluorescent systems, their strong fluorescence in dilute solutions will be weakened or quenched when their molecules are aggregated in poor solvents or they are fabricated as
solid their films. Such "aggregation-caused quenching" (ACQ) effect has greatly limited
their scope for high-technological applications.
In 2001, an opposite phenomenon to ACQ called "aggregation-induced emission"
(AIE) was discovered. Luminogens with AIE characteristics are generally
non-luminescent in solutions but emit intensely in the aggregated state. They thus solve
the ACQ problem and meanwhile open up a brand-new platform for exploring
biological applications.
Based on the AIE mechanism, restriction of intramolecular motion, the emission of
AIE luminogens (AIEgens) can be turned on through binding to various biomacromolecules, such as phospholipid, DNA and proteins, allowing analyte
qualification and quantitation, native/denatured protein differentiation, protein
fibrillation monitoring and electrophoretic gel visualization.
Thanks to the outstanding biocompatibility of AIEgens, they can be utilized for
visualizing and tracking cellular activities. In addition to their superior photostability
and long-term persistence in cell, detailed insight on the physiological events can be
achieved.
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