Impacts of sequence and structure on pyrrolocytosine fluorescence in RNA

Abstract

Fluorescence spectroscopy encompasses many useful methods for studying the structures and dynamics of biopolymers. Applications to nucleic acids require the use of extrinsic fluorophores such as fluorescent base analogues (FBAs), which mimic the native bases but have enhanced fluorescence quantum yields. In this work, we use multiple complementary methods to systematically investigate the sequence- and structure-dependence of the fluorescence of the FBA pyrrolocytosine (pC) within RNA. We demonstrate that pC is typically brightest in conformations in which it is base-stacked but not base-paired, properties that distinguish it from more widely used FBAs. This effect is strongly sequence-dependent, with adjacent adenosine and cytidine residues conferring the greatest contrast between stacked and unstacked structures. Structural heterogeneity was resolved in single-stranded RNA and fully complementary and mismatched double-stranded RNA using time-resolved fluorescence measurements and fluorescence-detected circular dichroism spectroscopy. Double-stranded contexts are distinguished from single-stranded contexts by the presence of inter-strand energy transfer from opposing bases, while base-paired pC is distinguished by its short excited state lifetime. This work will enhance the value of pC as a structural probe for biologically and medicinally significant RNAs by guiding the selection of labeling sites and interpretation of the resulting data. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=81 SRC="FIGDIR/small/618031v2_ufig1.gif" ALT="Figure 1"> View larger version (17K): org.highwire.dtl.DTLVardef@17fe2c1org.highwire.dtl.DTLVardef@1001feforg.highwire.dtl.DTLVardef@130b5a9org.highwire.dtl.DTLVardef@e692dd_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOGRAPHICAL ABSTRACTC_FLOATNO C_FIG