METHODS IN MOLECULAR BIOLOGY™ 335 FFlluuoorreesscceenntt EEnneerrggyy TTrraannssffeerr NNuucclleeiicc AAcciidd PPrroobbeess DDeessiiggnnss aanndd PPrroottooccoollss EEddiitteedd bbyy VVllaaddiimmiirr VV.. DDiiddeennkkoo,, ,, MMDD PPhhDD Fluorescent Energy Transfer Nucleic Acid Probes M E T H O D S I N M O L E C U L A R B I O L O G Y™ John M. Walker, SERIES EDITOR 357. Cardiovascular Proteomics: Methods and Proto- 329. Embryonic Stem Cell Protocols, Second Edition, cols, edited by Fernando Vivanco, 2006 Vol. I: Isolation and Characterization, edited by 356. Cellomics: Methods and Protocols, edited by Ken Kursad Turksen, 2006 Guiliano, D. Lansing Taylor, and Jeffrey Haskins, 2006 328. New and Emerging Proteomic Techniques, ed- 355. Plant Proteomics: Methods and Protocols, edited ited by Dobrin Nedelkov and Randall W. Nelson, 2006 by Hervé Thiellement, Michel Zivy, Catherine 327.Epidermal Growth Factor: Methods and Protocols, Damerval, and Valerie Mechin, 2006 edited by Tarun B. 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Didenko, , MD PhD Baylor College of Medicine, Houston, TX © 2006 Humana Press Inc. 999 Riverview Drive, Suite 208 Totowa, New Jersey 07512 www.humanapress.com All rights reserved. No part of this book may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, microfilming, recording, or otherwise without written permission from the Publisher. Methods in Molecular BiologyTM is a trademark of The Humana Press Inc. All papers, comments, opinions, conclusions, or recommendations are those of the author(s), and do not necessarily reflect the views of the publisher. This publication is printed on acid-free paper. ∞ ANSI Z39.48-1984 (American Standards Institute) Permanence of Paper for Printed Library Materials. Production Editor: Melissa Caravella Cover design by Patricia F. Cleary Cover illustration: Apoptotic rat thymus triple-stained by oscillating probe and fluorescent blue dye DAPI. Two types of DNA breaks are labeled with green and red fluorophores. Description of the probe is in Chapter 5, "Oscillating Probe for Dual Detection of 5'PO and 5'OH DNA Breaks in Tissue Sections," by Vladimir 4 V. Didenko. Image supplied by Vladimir V. Didenko. For additional copies, pricing for bulk purchases, and/or information about other Humana titles, contact Humana at the above address or at any of the following numbers: Tel.: 973-256-1699; Fax: 973-256-8341; E-mail: [email protected]; or visit our Website: www.humanapress.com Photocopy Authorization Policy: Authorization to photocopy items for internal or personal use, or the internal or personal use of specific clients, is granted by Humana Press Inc., provided that the base fee of US $30.00 per copy is paid directly to the Copyright Clearance Center at 222 Rosewood Drive, Danvers, MA 01923. For those organizations that have been granted a photocopy license from the CCC, a separate system of payment has been arranged and is acceptable to Humana Press Inc. The fee code for users of the Transactional Reporting Service is: [1-58829-380-7/06 $30.00]. Printed in the United States of America. 10 9 8 7 6 5 4 3 2 1 eISBN 1-59745-069-3 ISSN 1064-3745 Library of Congress Cataloging in Publication Data Fluorescent energy transfer nucleic acid probes : designs and protocols / edited by Vladimir V. Didenko. p. ; cm. -- (Methods in molecular biology ; v. 335) Includes bibliographical references and index. ISBN 1-58829-380-7 (alk. paper) 1. Nucleic acid probes. [DNLM: 1. Nucleic Acid Probes. 2. Fluorescence Resonance Energy Transfer--methods. 3. Genetic Techniques. QU 58 F647 2006] I. Didenko, Vladimir V. II. Series: Methods in molecular biology (Clifton, N.J.) ; v. 335. QP624.5.D73F558 2006 572.8'4--dc22 2005023841 Preface Fluorescent nucleic acid probes, which use energy transfer, include such constructs as molecular beacons, molecular break lights, Scorpion primers, TaqMan probes, and others. These probes signal detection of their targets by changing either the intensity or the color of their fluorescence. Not surpris- ingly, these luminous, multicolored probes carry more flashy names than their counterparts in the other fields of molecular biology. In recent years, fluores- cent probes and assays, which make use of energy transfer, have multiplied at a high rate and have found numerous applications. However, in spite of this explosive growth in the field, there are no manuals summarizing different pro- tocols and fluorescent probe designs. In view of this, the main objective of Fluorescent Energy Transfer Nucleic Acid Probes: Designs and Protocols is to provide such a collection. Oligonucleotides with one or several chromophore tags can form fluores- cent probes capable of energy transfer. Energy transport within the probe can occur via the resonance energy transfer mechanism, also called Förster trans- fer, or by non-Förster transfer mechanisms. Although the probes using Förster transfer were developed and used first, the later non-Förster-based probes, such as molecular beacons, now represent an attractive and widely used option. The term “fluorescent energy transfer probes” in the title of this book covers both Förster-based fluorescence resonance energy transfer (FRET) probes and probes using non-FRET mechanisms. Energy transfer probes serve as molecule-size sensors, changing their fluorescence upon detection of various DNA reactions. Many types of energy transfer probes can be adapted for homogenous detection formats, i.e., they function autonomously and fluorescently indicate their molecular targets with- out additional intervention. In this case, the energy transfer phenomenon serves as a “molecular cloaking device,” hiding the probe’s fluorescence until it detects its target. In the nonreactive state, probe fluorescence is quenched as a result of energy transfer to a nonfluorescent acceptor located in close proxim- ity to a fluorophore. After the reaction, relative positions of a fluorophore and a quencher change, resulting in the appearance of fluorescence. The DNA-based energy transfer constructs can also form “composition fluorophores” in which the emission and absorption properties can be indepen- dently tuned, making them attractive for the multiplex detection assays. v vi Preface Energy transfer probes are especially advantageous when used in multiplex polymerase chain reaction, as parts of biosensor assays, for screening and real- time monitoring of biochemical reactions, and in nanotechnology applications. Fluorescent Energy Transfer Nucleic Acid Probes: Designs and Protocols presents a wide assortment of methods using both Förster and non-Förster mechanisms of energy transfer in nucleic acids. A broad array of structures and applications of various energy transfer constructs and their optimized design are presented in detail for the first time. The techniques described include those designed to monitor various types of DNA and RNA reactions including hybridization, amplification, cleavage, folding, and association with proteins, other molecules, and metal ions. This volume also presents techniques for distance determination in protein–DNA complexes and methods to detect topological DNA alterations, mutations, and single nucleotide polymorphisms. It contains the latest cutting-edge nanotechnology applications, such as nanomachines, energy transfer aptazymes, DNAzyme-based biosensors, and logic gates for molecular-scale computation. Reproduction of technical protocols, readily available from original journal papers, would not warrant an additional publication. Fluorescent Energy Trans- fer Nucleic Acid Probes: Designs and Protocols instead serves as a compre- hensive source of information on every method described. The volume is divided into seven sections consisting of two to five chapters. The first section contains two chapters describing basic principles of selection and optimization of labels for FRET-based (Chapter 1) and non-FRET-based (Chapter 2) probes applicable to all energy transfer constructs. The section provides information necessary for the individualized design of energy trans- fer probes considering the specific needs of a researcher. Parts II–VI discuss application of energy transfer probes for detection and monitoring of various reactions involving DNA or RNA including: hybridization detection (Chapters 3 and 4), DNA breaks and cleavage monitoring (Chapters 5–7), synthesis and amplification visualization (Chapters 8–12), sequence analysis and mutation detection (Chapters 13–16), and determination of distances and DNA folding (Chapters 17–18). The last section (Chapters 19–22) deals with design and application of molecular devices that use energy transfer, such as biosensors, nanomachines, and logic gates for molecular-scale computation. Chapter 5 describes a molecular machine for DNA breaks detection and therefore belongs to both the nanotechnology and DNA damage fields. The field of fluorescent probes is constantly evolving and I hope that this volume will not only help its readers use the described techniques, but will prompt them to explore new ways in which energy transfer constructs can facilitate their research. vii Preface Researchers using fluorescence in any field of biomedical sciences will ben- efit from this book. These include molecular and cell biology, embryology, toxicology, radiobiology, experimental and clinical pathology, oncology, experimental pharmacology, drug design, environmental science, and nanotechnology. Fluorescent Energy Transfer Nucleic Acid Probes: Designs and Protocols is a helpful resource for both novice investigators and experi- enced researchers. For a scientist new to the area of fluorescent probes, the book will help to select the suitable probe, to deal with experimental pitfalls and to properly interpret the results. Experienced researchers will find the book useful because it describes the new and unique constructs in detail and can be used as a source of information in development of new energy transfer probes and applications. I am grateful to all participating authors whose ingenuity made this book possible, and particularly to those of them who submitted their contributions on time. I wish to express my appreciation to Candace Minchew for her expert technical assistance. I also thank Professor John Walker for his generous help with the review process. Vladimir V. Didenko, MD, PhD Contents Preface ..............................................................................................................v Contributors ...................................................................................................xiii Companion CD...............................................................................................xv PART I. DESIGN OF ENERGY TRANSFER PROBES 1 Selection of Fluorophore and Quencher Pairs for Fluorescent Nucleic Acid Hybridization Probes Salvatore A. E. Marras..........................................................................3 2 Choosing Reporter–Quencher Pairs for Efficient Quenching Through Formation of Intramolecular Dimers Mary Katherine Johansson..................................................................17 PART II.ENERGY TRANSFER PROBES FOR DNA AND RNA HYBRIDIZATION DETECTION AND MONITORING 3 Detection of DNA Hybridization Using Induced Fluorescence Resonance Energy Transfer W. Mathias Howell.............................................................................33 4 Detecting RNA/DNA Hybridization Using Double-Labeled Donor Probes With Enhanced Fluorescence Resonance Energy Transfer Signals Yukio Okamura and Yuichiro Watanabe............................................43 PART III. ENERGY TRANSFER PROBES FOR DNA BREAKS DETECTION AND DNA CLEAVAGE MONITORING 5 Oscillating Probe for Dual Detection of 5’PO and 5’OH DNA 4 Breaks in Tissue Sections Vladimir V. Didenko...........................................................................59 6 Using Molecular Beacons for Sensitive Fluorescence Assays of the Enzymatic Cleavage of Nucleic Acids Chaoyong James Yang, Jeff Jianwei Li, and Weihong Tan.................71 7 A Continuous Assay for DNA Cleavage Using Molecular Break Lights John B. Biggins, James R. Prudent, David J. Marshall, and Jon S. Thorson.........................................................................83 ix
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