SHERP

Single-Molecule Study of the Enzymatic Mechanism and Kinetics of 10-23 Deoxyribozyme using Total Internal Reflection Fluorescence Microscopy
전반사 형광 현미경법을 이용한 10-23 디옥시라이보자임의 효소적 메커니즘과 동역학에 대한 단분자 연구

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Authors
김선영
Advisor
김성근
Major
자연과학대학 생물물리 및 화학생물학과
Issue Date
2015
Publisher
서울대학교 대학원
Keywords
10-23 DeoxyribozymeKineticsEnzymatic MechanismSingle-MoleculeTotal Internal Reflection Fluorescence MicroscopyFluorescence Resonance Energy Transfer
Description
학위논문 (석사)-- 서울대학교 대학원 : 생물물리 및 화학생물학과, 2015. 2. 김성근.
Abstract
Total internal reflection fluorescence (TIRF) microscopy, with the aid of the fluorescence resonance energy transfer (FRET) phenomenon, enables the real-time observation of nanometer-scale structural changes, which are often hidden in ensemble measurements, from a fluorescently labeled single biomolecule. Using TIRF microscopy, we investigated the stepwise enzymatic reaction mechanism of 10-23 deoxyribozyme, an RNA-cleaving DNA enzyme which has been widely studied in various fields of applied science. First, we analyzed the kinetics of the four normal reaction sub-steps of 10-23 deoxyribozyme of enzyme-substrate binding, substrate cleavage, and dissociations of each of the two products by varying the molecular environments specifically the temperature, the pH, and the residue of the cleavage site. Kinetic parameters and rates depending on the environmental changes revealed significant features with regard to the molecular mechanisms of each reaction. Secondly, we identified two additional individual reaction sub-steps which involve the half-binding of a new substrate before the second product dissociation that we termed “shortcut binding” and the subsequent strand displacement of the remaining product by the half-bound substrate. We determined that shortcut binding and strand displacement can occur and conducted a kinetic analysis of each reaction sub-step while varying the substrate concentration. Shortcut binding occurs more frequently at a higher substrate concentration and the rate of shortcut binding and the second dissociation are dependent on the substrate concentration, as the two reactions compete with each other. We calculated the rate equation, noting that shortcut binding accelerates the enzymatic turnover rate. To sum up, by adapting TIRF, we revealed the characteristics of 10-23 deoxyribozyme. These may be essential in the study of the chemical mechanisms and for explorations of the wider use of catalytic nucleic acids.
Language
English
URI
http://hdl.handle.net/10371/131527
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College of Natural Sciences (자연과학대학)Biophysics and Chemical Biology (생물물리 및 화학생물학과)Theses (Master's Degree_생물물리 및 화학생물학과)
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