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. 2009 Jan 16;37(4):1353–1362. doi: 10.1093/nar/gkn1088

Table 2.

Comprehensive investigation of nuclease stability of chemically modified ONsa

S1 nuclease
SVPD
50% human plasma
ON t1/2b t1/2c t1/2 t1/2 Degradation pattern
RNA1 25.4 ± 7.2 s 6.0 ± 0.6 min < 10 s Endo
DNAl 7.4 ± 1.9 s 3.1 ± 0.1 min 46.8 ± 7.0 min Exo
MeRNAI >24 h 224 ± 47.6 min 5.3 ± 1.5 min 187 ± 22.6 min Exo
SRNA1 76.8 ± 25.2 min 54.4 ± 2.5 min 65.7 ± 8.0 min Endo
Me-SRNAl >24 h >24 h 79.2 ± 8.7 min 1631 ± 60.8 min Exo
FRNA1 1.1 ± 0.1 min 5.8 ± l.2 min 53.2 ± 3.5 min Exo
RNA2 13.0 ± 2.4 s 4.3 ± 0.4 min < 10 s Endo
DNA2 6.6 ± 1.3 s 2.7 ± 0.3 min 31.0 ± 1.7 min Exo
FRNA2 20.8+0.4 s 6.0 ± 1.0 min 51.9 ± 3.1 min Exo
SRNA2 12.6 ± 1.7 min 12.8 ± 3.5 min < 10 s Endo
F-SRNA2 6.5 ± 0.5 min 21.0 ± 3.6 min 120 ± 10.5 min Exo
MeRNA2 >24 h 136 ± 11.5 min 4.5 ± 1.1 min 435 ± 12.9 min Exo

aErrors reflect standard deviation from three independent experiments.

bONs were treated with 0.17 U/µL S1 nuclease.

cONs were treated with 51 U/µL S1 nuclease.