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Guidelines for selection of sgRNAs for protein knockout experiments based on nCas9 (NGG PAM requirements) and rat APOBEC deaminase.
  1. Using manual methods or publicly available base editing guide RNA design tools (see example resources section, or appendix A), generate lists of candidate sgRNA protospacer (targeting) sequences for your purpose based on the transcript of interest:
    1. Generate premature stop codons for protein knockout by designing sgRNAs with NGG PAMs that allow the conversion of CAA, CAG, CGA, or TGG codons into STOP codons (Figure 1) when the target C(s) are located within position 3 to 8 of the spacer sequence in the 5'-3' direction (Figure 2)1.
    2. Generate splice site disruptions for protein knockout:
      1. Design sgRNAs with an NGG PAM that locate the target C within position 3 to 8 of the spacer sequence in the 5'-3' direction (Figure 2)1;
      2. Splice acceptor site is generally: intron-AG|exon;
      3. Splice donor site is generally exon|GT-intron;
      4. Converting the GC base pair to an AT base pair will lead to splice site disruption2.
  2. Further refine candidate lists by the following criteria, if necessary:
    1. Consider your gene structure to select a subset of gRNAs with highest probability to result in protein knockout:
      1. Avoid gRNAs that target the earliest and/or latest exons;
      2. Give higher priority to gRNAs that targets the middle part of the protein, with preference for gRNAs located within the middle 10-60% of your transcript – if necessary to find additional gRNA candidates, look beyond 60% into the CDS until sufficient guides are found;
      3. Give preference to gRNAs that target exon coding for essential domains in the protein (i.e transmembrane domain for receptors);
      4. Target non-symmetric exons. If a symmetric exon is targeted, and the targeted exon is skipped, the following exons will be in-frame3;
      5. Ensure the sgRNA targets all required isoforms.
    2. Prioritize guides based on the 2 nt 5' of the target C3:
      1. Give preference where the sequence context is NTC and TCC;
      2. Avoid where the sequence context is NGC and GCC.

Stop codons

Figure 1. Stop codons that can be generated from a cytidine deamination1

 

Base editing window
Base editing window
Figure 2.  Dark green= potential for highest efficiency editing. Light green= potential for lower efficiency editing. White= potential for bystander editing. 

Figure 2. Base editing window. Dark green= potential for highest efficiency editing. Light green= potential for lower efficiency editing. White= potential for bystander editing.

References
  1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610906 (see figure 1)
  2. https://www.nature.com/articles/s41467-021-22009-2 (see figure 1)
  3. Poster - Performance and modularity of Horizon’s Pin-point™ base editing system characterized by arrayed and pooled screening platforms
Additional External Resources

All custom sgRNA sequences must be experimentally validated. These guidelines and suggestions are without guarantee of functionality. Specificity of sgRNA sequences should always be considered to reduce off-target effects.

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