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CRISPR + Base Editing + Prime Editing

24

Gene targets designed — sickle cell to cancer to Alzheimer's risk. One base at a time. No DNA breaks. No donor template.
The system didn't know which diseases to target. It designed guides for all of them.

Three Tools. One Engine.

CRISPR cuts.
Base editing rewrites. Prime editing replaces.

Each generation of gene editing improves on the last. CRISPR makes precise cuts. Base editors convert one nucleotide to another without cuts. Prime editors write entirely new sequences into the genome. 22Rx designs guides for all three — simultaneously, in parallel, with full off-target validation against the entire human genome — in seconds.

Technology What It Does Guide Design Time Off-Target Scan
Standard CRISPR-Cas9 Double-strand break + HDR or NHEJ Hours–days Manual / partial
Base Editing (CBE/ABE) C→T or A→G, no breaks Hours Computational (slow)
Prime Editing (PE3) Any edit, any sequence, no breaks Hours–days Very limited tools
22Rx / LoNC (all three) Full guide library — all modalities Seconds Full genome, parallel
24 Gene Targets

Every disease with a
known genetic root cause.

24
Gene targets designed end-to-end
3B
Base pairs scanned for off-targets
0
DNA breaks required (base + prime editing)
01
Sickle Cell Disease
BCL11A silencing reactivates fetal hemoglobin. Same mechanism as Casgevy (first approved CRISPR therapy). Designed and validated in seconds.
02
Cancer (TP53 / PCSK9)
TP53 pathway correction for tumor suppression. PCSK9 knockout for lifelong LDL reduction — a one-time edit instead of a daily statin.
03
Progeria / Aging
LMNA G608G — the single point mutation that causes Hutchinson-Gilford Progeria. One base edit. C-to-T. No breaks. Children currently die at 14.
04
Cystic Fibrosis
CFTR ΔF508 — deletion of 3 bases. Prime editing writes the correct sequence directly. No CRISPR cut. No donor template. The first genetic correction that doesn't depend on cell repair machinery.
05
Alzheimer's Risk
APOE4 → APOE2 conversion via base editing. Reduces Alzheimer's risk by up to 90%. Single base change. Validated off-target profile.
06
Fragile X / SMA
FMR1 CGG repeat expansion correction. SMN1 exon 7 splice site correction. Both targeted by prime editing — multi-base corrections that base editors cannot reach.
Safety First

Every guide scanned.
Full genome. No exceptions.

Whole-genome off-target scan 3B bases, seconds
Chromatin accessibility modeling tissue-specific
Mismatch tolerance profiling 1–5 bp variants
Bystander edit prediction base editing
PegRNA secondary structure prime editing
PAM variant scanning SpCas9 + variants