Population
In vitro and in vivo models of HIV-1 Tat-TAR interaction
Comparison
Nucleotide substitutions and synthetic propyl… vs Wild-type TAR RNA
Design
Preclinical
Authors
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TAR stem substitutions block Tat binding in models; leaves open therapeutic targeting of this interface in human HIV.
Uridine 23 in the TAR RNA bulge forms a stable tertiary interaction with the GC pair directly above it, widening the major groove to expose hydrogen-bonding surfaces for Tat recognition.
Delling et al. (1992) studied this question.
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