Chow, Christine S. (1992) Transition metal complexes as probes for higher-order structure in RNA. Dissertation (Ph.D.), California Institute of Technology. http://resolver.caltech.edu/CaltechTHESIS:10142011-105722078
A series of transition metal complexes were employed to examine higher-order structure in ribonucleic acids. Our results indicate that the complexes Ru(phen)_3^(2+), Ru(TMP)_3^(2+), Rh(TMP)_3^(3+), Rh(phen)_2phi^(3+), Rh(phi)_2bpy^(3+), and Rh(DIP)_3^(3+) (phen = 1,10-phenanthroline; TMP = 3,4,7,8,-tetramethy1-1,10-phenanthroline; phi = 9,10- phenanthrenequinone diimine; bpy = bipyridyl; DIP = 4,7-dipheny1-1,10-phenanthroline) have different affinities for tRNA and bind RNA by several different modes of interaction, as shown through a variety of biophysical analyses. These differences in binding have been attributed to the different shapes of the metal complexes. Photolysis of the metal complexes promotes cleavage of native, structured RNA at diverse and novel sites with comparable efficiency and analogous product formation as found with cleavage of double-stranded DNA. As on DNA, RNA strand scission promoted by the complexes of rhodium(III) occurs through an oxidative pathway with the sugar moiety as the target. Reactions with the complexes of ruthenium(II) are consistent with mediation by singlet oxygen with the nucleic acid base as the target. The site selectivity associated with cleavage appears to be based upon the different binding properties and therefore the molecular shapes of the complexes. Ru(TMP)_3^(3+) cleaves at a subset of solvent accessible sites cleaved by Ru(phen)_3^(2+). Different sites of cleavage on tRNA are apparent with the rhodium complexes, Rh(phen)_2phi^(3+), Rh(phi)_2bpy^(3+), and Rh(DIP)_3^(3+), while Rh(TMP)_3^(3+) does not promote strand scission of RNA. In particular, Rh(phen)_2phi^(3+) targets sites of triple-base interaction, D-TΨC loop interactions, and helix-loop junctions in tRNA, where the major groove is open and accessible. Rh(DIP)_3^(3+) targets RNA loop structures and G-U mismatches that occur within an RNA double-helix. These shape-selective probes, which promote strand scission of tRNA at unique sites, have also been applied to probe mutant tRNAs and to delineate the structure of 5S rRNA. This study demonstrates that small molecules can recognize distinct structures along an RNA strand and suggests that these structures may be utilized for specific recognition by proteins.
|Item Type:||Thesis (Dissertation (Ph.D.))|
|Degree Grantor:||California Institute of Technology|
|Division:||Chemistry and Chemical Engineering|
|Thesis Availability:||Restricted to Caltech community only|
|Defense Date:||20 January 1992|
|Default Usage Policy:||No commercial reproduction, distribution, display or performance rights in this work are provided.|
|Deposited By:||Julie Guan|
|Deposited On:||14 Oct 2011 20:16|
|Last Modified:||26 Dec 2012 04:39|
- Final Version
Restricted to Caltech community only
See Usage Policy.
Repository Staff Only: item control page