Nucleic Acids Research, Vol 24, Issue 12 2220-2227, Copyright © 1996 by Oxford University Press
J Hamm
Constrained RNA libraries of limited sequence complexity were constructed
and used to select RNA molecules binding to the antigen binding site of an
anti-ferritin antibody. The sequences required as primer-binding sites for
the selection cycle were designed to form a predictable secondary
structure, which greatly facilitated the characterisation of the secondary
structures of the selected RNAs. RNA- antibody interactions were studied by
real-time interaction analysis to study the dynamic aspects of binding and
by circular dichroism spectroscopy to search for conformational changes
upon binding. The selected RNAs were analysed with a binding site
sequestering assay and were shown to compete with ferritin for binding to
the antigen-binding site. The experiments described here indicate that the
introduction of strong structural constraints does not have to interfere
with the ability to select tightly and specifically binding RNA-molecules.
ARTICLES
Characterisation of antibody-binding RNAs selected from structurally constrained libraries
Istituto di Ricerche di Biologia Molecolare, Roma, Italy.
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