Curved oligonucleotide constructs as human topoisomerase I inhibitors : a mechanistic study of the enzyme’s recognizing passway.

• المؤلف الرئيسي: Zhao, Guanjia.
• مؤلفون آخرون: School of Physical and Mathematical Sciences
• التنسيق: Final Year Project
• اللغة: English
• منشور في: 2010
• الموضوعات: DRNTU::Science::Biological sciences::Biochemistry
• الوصول للمادة أونلاين: http://hdl.handle.net/10356/38601
• المؤسسة: Nanyang Technological University

Topoisomerases I are enzymes that alter the topological states of DNA. In eukaryotic organisms, including human being, Topoisomerase I is diverse and significant. It is discovered that there are more than normal amount of Topo I enzymes in the tumour cells, making it a potential drug target for cancer therapy. The traditional Topo I inhibitors are organic molecules, and this report aims to develope short oligonucleotides as possible Topo I inhibitors, and also to study the recognition mechanism of human Topoisomerase I with the substrate DNA molecules. In this project, it was not only evidenced that DNA curvature indeed was crucial for the enzyme-substrate recognition, but also the minimum number of A-tracts in the curved constructs was determined. What’s more, inhibitory effects of different types of curvature on Topo I were compared to show that a two-way-curved oligonucleotide was more effective to inhibit Topo I activity than the corresponding one-way-curved oligonucleotide, and this finding might be helpful for better understanding of the enzyme-DNA recognition mechanism.