TY - JOUR
T1 - Biophysical Studies of the Translation Initiation Pathway with Immobilized mRNA Analogs
AU - Mccarthy, John
AU - McCarthy, John E G
AU - Marsden, Steven
AU - von der Haar, Tobias
PY - 2007
Y1 - 2007
N2 - A growing number of biophysical techniques use immobilized reactants for the quantitative study of macromolecular reactions. Examples of such approaches include surface plasmon resonance, atomic force microscopy, total reflection fluorescence microscopy, and others. Some of these methods have already been adapted for work with immobilized RNAs, thus making them available for the study of many reactions relevant to translation. Published examples include the study of kinetic parameters of protein/RNA interactions and the effect of helicases on RNA secondary structure. The common denominator of all of these techniques is the necessity to immobilize RNA molecules in a functional state on solid supports. In this chapter, we describe a number of approaches by which such immobilization can be achieved, followed by two specific examples for applications that use immobilized RNAs. © 2007 Elsevier Inc. All rights reserved.
AB - A growing number of biophysical techniques use immobilized reactants for the quantitative study of macromolecular reactions. Examples of such approaches include surface plasmon resonance, atomic force microscopy, total reflection fluorescence microscopy, and others. Some of these methods have already been adapted for work with immobilized RNAs, thus making them available for the study of many reactions relevant to translation. Published examples include the study of kinetic parameters of protein/RNA interactions and the effect of helicases on RNA secondary structure. The common denominator of all of these techniques is the necessity to immobilize RNA molecules in a functional state on solid supports. In this chapter, we describe a number of approaches by which such immobilization can be achieved, followed by two specific examples for applications that use immobilized RNAs. © 2007 Elsevier Inc. All rights reserved.
U2 - 10.1016/S0076-6879(07)30010-4
DO - 10.1016/S0076-6879(07)30010-4
M3 - Article
SN - 0076-6879
VL - 430
SP - 247
EP - 264
JO - Methods in Enzymology
JF - Methods in Enzymology
ER -