HiTS-RAP is a quantitative method to evaluate binding interactions of RNA aptamers with their proteins at a massive scale. , HiTS-RAP transcribes DNA directly on the flow cell and measures the binding affinity of RNA aptamers with fluorescently labeled proteins.
First, sequencing libraries are prepared and sequenced on the Illumina flow cell. Next, the second strand of the DNA is removed and the single-stranded DNA attached to the flow cell is annealed to primers containing a 32 bp Ter sequence. An Escherichia coli replication terminator protein (Tus) is introduced into the system and binds to the Ter sequence. RNA transcription by T7 RNA polymerase begins and halts upstream of the Tus-bound Ter site. Because the RNA polymerase activity was halted abruptly due to the Tus bound to the DNA, the RNA strand is still linked to the RNA polymerase complex. Fluorescently labeled proteins are introduced and bind to the exposed RNA aptamers, producing a fluorescent signal that can be read by the sequencer.
Similar methods: RBNS, RNA-MaP.