Contributors | p. xi |
Preface | p. xv |
Volumes in Series | p. xvii |
Chemical and Functional Probing of RNA Structure, Interactions, and Folding | p. 1 |
Nucleotide Analog Interference Mapping | p. 3 |
Introduction | p. 4 |
Materials and Reagents | p. 7 |
Methods | p. 9 |
Properties of Analogs | p. 19 |
Nucleotide Analog Interference Suppression | p. 25 |
Conclusions | p. 26 |
References | p. 27 |
Hydroxyl-Radical Footprinting to Probe Equilibrium Changes in RNA Tertiary Structure | p. 31 |
Introduction | p. 32 |
Sample Preparation | p. 34 |
Equilibrium òOH Footprinting Based on Peroxidative Fenton Chemistry | p. 35 |
Equilibrium òOH Footprinting Based on Oxidative Fenton Chemistry | p. 36 |
Cleavage Product Separation | p. 38 |
Quantitation of the Changes in the Reactivity and Data Analysis | p. 40 |
Conclusions | p. 44 |
Acknowledgments | p. 44 |
References | p. 44 |
Rapid Quantification and Analysis of Kinetic òOH Radical Footprinting Data Using SAFA | p. 47 |
Introduction | p. 48 |
Using SAFA | p. 50 |
Data Normalization | p. 57 |
Data Visualization | p. 61 |
Conclusion | p. 64 |
Acknowledgment | p. 64 |
References | p. 65 |
High-Throughput SHAPE and Hydroxyl Radical Analysis of RNA Structure and Ribonucleoprotein Assembly | p. 67 |
Introduction | p. 68 |
Theory | p. 70 |
Practice | p. 73 |
Examples and Interpretation | p. 78 |
Perspectives and Conclusion | p. 86 |
Acknowledgments | p. 86 |
References | p. 87 |
Metal Ion-Based RNA Cleavage as a Structural Probe | p. 91 |
Introduction | p. 92 |
Mechanisms of Metal Ion-Based Cleavage of Nucleic Acids | p. 92 |
Metal Ion-Based Cleavage of RNA as a Structural Probe | p. 95 |
Protocols | p. 98 |
Acknowledgment | p. 103 |
References | p. 103 |
2'-Amino-Modified Ribonucleotides as Probes for Local Interactions Within RNA | p. 107 |
Introduction | p. 108 |
2'-Amino-2'-Deoxynucleotide Synthesis and Incorporation | p. 110 |
2'-Amino-2'-Deoxynucleotides as Sites for Covalent Modification | p. 111 |
General Strategy for Investigating 2'-Hydroxyl Interactions Using 2'-Deoxy and 2'-Aminonucleotides | p. 112 |
Studies of RNA Catalysis Using 2'-Amino-2'-Deoxynucleotides | p. 114 |
Using 2'-Aminonucleotides to Investigate RNA Structure and Function: Case Studies | p. 116 |
Conclusions | p. 121 |
Acknowledgments | p. 121 |
References | p. 122 |
RNA Crosslinking Methods | p. 127 |
Introduction | p. 128 |
Synthesis of Modified RNA Crosslinking Substrates | p. 129 |
Generation of Crosslinked RNAs | p. 135 |
Mapping of Crosslinked Nucleotides | p. 139 |
Assessing the Validity of Crosslinking Data | p. 141 |
References | p. 143 |
Chemical Probing of RNA and RNA/Protein Complexes | p. 147 |
Introduction | p. 148 |
Materials | p. 150 |
Handling of the Chemicals | p. 151 |
Optimization of the Chemical Probing Reactions | p. 152 |
Procedure of Chemical Probing | p. 154 |
RNA Extraction | p. 159 |
Normalization of the RNA Sample | p. 160 |
Primer Extension Analysis | p. 160 |
Data Evaluation | p. 162 |
Summary | p. 164 |
Acknowledgments | p. 164 |
References | p. 164 |
RNA Folding During Transcription: Protocols and Studies | p. 167 |
Introduction | p. 168 |
Protocol 1: Determination of Transcriptional Pause Sites | p. 169 |
Protocol 2: Structural Mapping of Paused Complexes | p. 172 |
Protocol 3: Cotranscriptional RNA Folding as Measured via Oligohybridization | p. 174 |
Protocol 4: Cotranscriptional RNA Folding Measured via P RNA Catalytic Activity | p. 175 |
Protocol 5: The Folding of Self-Cleaving RNAs During Transcription | p. 179 |
Additional Methodologies | p. 181 |
Cotranscriptional Folding Studies from our Laboratory | p. 181 |
References | p. 190 |
Catalytic Activity as a Probe of Native RNA Folding | p. 195 |
Introduction | p. 196 |
Preliminary Measurements of Catalytic Reaction | p. 199 |
Following RNA Folding by Continuous Activity Assay | p. 203 |
Following RNA Folding by Discontinuous Activity Assay | p. 206 |
Other Applications of Catalytic Activity as a Probe of Folding | p. 209 |
Acknowledgments | p. 215 |
References | p. 215 |
Probing RNA Structure Within Living Cells | p. 219 |
Introduction | p. 220 |
Experimental Procedure | p. 221 |
Application | p. 234 |
Limitations | p. 235 |
Conclusion | p. 236 |
Acknowledgments | p. 236 |
References | p. 236 |
Structural Analysis of RNA in Living Cells by In Vivo Synchrotron X-Ray Footprinting | p. 239 |
Introduction | p. 240 |
Beamline Setup for In Vivo Footprinting | p. 241 |
Preparation of Samples | p. 242 |
Exposure of Cells to X-Ray Beam | p. 244 |
Isolation of Total RNA from Irradiated Cells | p. 247 |
Primer Extension | p. 248 |
Analysis of X-Ray Footprinting Experiments | p. 251 |
Results on E. coli RNAs | p. 253 |
Future of Footprinting | p. 255 |
Acknowledgments | p. 255 |
References | p. 255 |
Determination of Intracellular RNA Folding Rates Using Self-Cleaving RNAs | p. 259 |
Introduction | p. 260 |
Using RNA Turnover Rates as a ôClockö for Measuring RNA Assembly Kinetics | p. 262 |
Applications | p. 280 |
Acknowledgments | p. 285 |
References | p. 285 |
Identifying Metal Ion Interactions in RNA | p. 287 |
Separation of RNA Phosphorothioate Oligonucleotides by HPLC | p. 289 |
Introduction: Phosphorothioate Oligonucleotides and the Need for Separation | p. 290 |
HPLC Separation of Phosphorothioate Diastereomers | p. 294 |
Materials and Methods | p. 298 |
Examples of Phosphorothioate Oligonucleotide Separations | p. 299 |
Acknowledgments | p. 307 |
References | p. 307 |
Use of Phosphorothioates to Identify Sites of Metal-Ion Binding in RNA | p. 311 |
Introduction | p. 312 |
Use of Phosphorothioate-Containing Ribozymes to Identify Sites of Metal-Ion Binding | p. 312 |
Protocols | p. 322 |
Acknowledgments | p. 330 |
References | p. 331 |
EPR Methods to Study Specific Metal-Ion Binding Sites in RNA | p. 335 |
Introduction | p. 336 |
Room Temperature EPR Spectroscopy to Quantify Mn2+ Bound to RNA | p. 341 |
Low-Temperature EPR Spectroscopy of Mn2+ Ions Bound to RNA | p. 345 |
ENDOR Spectroscopy to Identify Metal Ligands | p. 350 |
ESEEM Spectroscopy | p. 357 |
Summary | p. 361 |
Acknowledgments | p. 364 |
References | p. 364 |
RNA Thermodynamics | p. 369 |
Optical Melting Measurements of Nucleic Acid Thermodynamics | p. 371 |
Introduction | p. 371 |
Instrumentation | p. 372 |
Calibrations | p. 373 |
Brief Theory of Optical Melting Experiments | p. 375 |
Two-State Assumption | p. 378 |
¿Cp°-Assumption | p. 378 |
Experimental Design | p. 378 |
Data Interpretation | p. 382 |
Error Analysis | p. 383 |
Summary | p. 384 |
Acknowledgments | p. 384 |
References | p. 384 |
Analyzing RNA and DNA Folding Using Temperature Gradient Gel Electrophoresis (TGGE) with Application to In Vitro Selections | p. 389 |
Introduction | p. 390 |
Temperature Gradient Gel Electrophoresis | p. 391 |
Experimental Design and Application of TGGE to RNA and DNA | p. 399 |
Acknowledgment | p. 406 |
References | p. 406 |
Studying RNA-DNA and RNA-Protein Interactions by Isothermal Titration Calorimetry | p. 409 |
Introduction | p. 410 |
Required Materials | p. 411 |
Instrumentation | p. 411 |
Sample Considerations and Preparation | p. 412 |
Cleaning the Sample Cell and Titration Syringe | p. 414 |
Collecting Titration Data | p. 415 |
Data Processing and Analysis | p. 418 |
Special Considerations | p. 420 |
Conclusions | p. 421 |
References | p. 422 |
Author Index | p. 423 |
Subject Index | p. 431 |
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