probing the structure of dna aptamers with a classic heterocycle.探索dna结构的寡核苷酸适配子与一个典型的杂环。.pdfVIP
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probing the structure of dna aptamers with a classic heterocycle.探索dna结构的寡核苷酸适配子与一个典型的杂环。
Molecules 2004, 9, 67–85
molecules
ISSN 1420-3049
Probing the Structure of DNA Aptamers with a Classic
Heterocycle.
Arthur E. Wood IV and G. Reid Bishop*
Department of Chemistry and Biochemistry, Mississippi College, 200 South Capitol St., Clinton, MS
39058. USA. Tel. +1 (601)-925-7665, Fax +1 (601)-925-3993.,
* Author to whom correspondence should be addressed; email rbishop@
Received: 5 February 2004; in revised form: 9 February 2004 / Accepted: 15 February 2004 /
Published: 28 February 2004
Abstract: DNA aptamers are synthetic, single-stranded DNA oligonucleotides selected
by SELEX methods for their binding with specific ligands. Here we present ethidium
binding results for three related DNA aptamers (PDB code: 1OLD, 1DB6, and 2ARG)
that bind L-argininamide (L-Arm). The ligand bound form of each aptamers structure
has been reported and each are found to be composed primarily of two domains
consisting of a stem helical region and a loop domain that forms a binding pocket for the
cognate ligand. Previous thermodynamic experiments demonstrated that the DNA
aptamer 1OLD undergoes a large conformational ordering upon binding to L-Arm. Here
we extend those linkage binding studies by examining the binding of the heterocyclic
intercalator ethidium to each of the three aptamers by fluorescence and absorption
spectrophotometric titrations. Our results reveal that ethidium binds to each aptamer with
∆Gos in the range of -8.7 to -9.4 kcal/mol. Th
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