RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
about
Pyrene is highly emissive when attached to the RNA duplex but not to the DNA duplex: the structural basis of this differenceFluorescence of covalently attached pyrene as a general RNA folding probe.Common and distinctive features of GNRA tetraloops based on a GUAA tetraloop structure at 1.4 A resolution.An early transition state for folding of the P4-P6 RNA domain.How a chemist looks at RNA.Multivector fluorescence analysis of the xpt guanine riboswitch aptamer domain and the conformational role of guanineEvaluation of dynamic features of Escherichia coli 16S ribosomal RNA in homogeneous physiological solution.Topological rearrangement yields structural stabilization and interhelical distance constraints in the Kin.46 self-phosphorylating ribozyme.Measuring the folding transition time of single RNA molecules.Dissection of the ion-induced folding of the hammerhead ribozyme using 19F NMR.Using pyrene-labeled HIV-1 TAR to measure RNA-small molecule binding.Uridine 2'-carbamates: facile tools for oligonucleotide 2'-functionalization.Kinetic and thermodynamic framework for P4-P6 RNA reveals tertiary motif modularity and modulation of the folding preferred pathway.Multiple conformational states of the hammerhead ribozyme, broad time range of relaxation and topology of dynamicsPermanent or reversible conjugation of 2'-O- or 5'-O-aminooxymethylated nucleosides with functional groups as a convenient and efficient approach to the modification of RNA and DNA sequences.Site-specific fluorescent labeling of large RNAs with pyrene.Pyrenemethyl ara-uridine-2'-carbamate: a strong interstrand excimer in the major groove of a DNA duplex.Polymerase-Mediated Site-Specific Incorporation of a Synthetic Fluorescent Isomorphic G Surrogate into RNA.Interactions of the N-terminal domain of ribosomal protein L11 with thiostrepton and rRNA.Site-specific fluorescent and affinity labelling of RNA by using a small engineered twin ribozyme.Photo-physical properties of 2-(1-ethynylpyrene)-adenosine: influence of hydrogen bonding on excited state properties.Convenient and efficient approach to the permanent or reversible conjugation of RNA and DNA sequences with functional groups.Interaction between beta-amyloid and lens alphaB-crystallin.Use of fluorescence spectroscopy to elucidate RNA folding pathways.Functionalization of 2″-C-(Piperazinomethyl)-2′,3′-BcNA (Bicyclic Nucleic Acids) with Pyren-1-ylcarbonyl Units
P2860
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P2860
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
description
1999 nî lūn-bûn
@nan
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@ast
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@en
type
label
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@ast
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@en
prefLabel
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@ast
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@en
P356
P1433
P1476
RNA tertiary folding monitored by fluorescence of covalently attached pyrene.
@en
P2093
P304
14224-14237
P356
10.1021/BI991333F
P407
P577
1999-10-01T00:00:00Z