Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/38616
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dc.contributor.authorZhang, Yi.-
dc.date.accessioned2010-05-13T08:01:09Z-
dc.date.available2010-05-13T08:01:09Z-
dc.date.copyright2010en_US
dc.date.issued2010-
dc.identifier.urihttp://hdl.handle.net/10356/38616-
dc.description.abstractHuman topoisomerase I is a group of enzyme that is responsible for the interconversions of different topological forms of DNA molecules in vivo. One of the most significant function of it is untangling the supercoiling in DNA molecules during cellular metabolic processes like replication and transcription, by introducing a transient breakage in one strand in order to make the opposing strand pass through freely and release the stress. This paper raised a new concern that DNA curvature plays a role in the binding of topoisomerase I to supercoiled DNA molecules, which suggested possible mechanisms for topoisomerase I recognition and interaction during its catalyzing reaction. DNA minicircles with relatively few base pairs were synthesized in order to mimic the supercoiling state of DNA molecules, and its binding to topoisomerase I was proven to be efficient, which suggested a future target for topoisomerase I inhibitor.en_US
dc.format.extent21 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Biochemistryen_US
dc.titleRecognition of forcibly curved DNA by human topoisomerase I.en_US
dc.typeFinal Year Project (FYP)en_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degreeBachelor of Science in Chemistry and Biological Chemistryen_US
dc.contributor.supervisor2Li Tianhuen_US
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Appears in Collections:SPMS Student Reports (FYP/IA/PA/PI)
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