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. 2005 Jun 13;33(10):e96. doi: 10.1093/nar/gni099

Table 1.

A listing of all detected ion signals of DNA fragments and E9 DNase–DNA complexes, their molecular masses and assignments

Abbreviation Ions (m/z) Mw (Da)
ssDNA fragments
    GTAAAACGACGGCCAGT 5′-17-3′ 1308.2 (4+), 1743.9 (3+) 5228.5
    GTAAAACGACGGCC 5′-14 1071.5 (4+), 1428.3 (3+) 4281.9
    GTAAAACGACGG 5′-12 1235.7 (3+) 3703.5
    GTAAAACGAC 5′-10 1016.1 (3+) 3045.1
    GTAAAAC 5′-7 1057.8 (2+) 2113.6
    GTAAAA 5′-6 913.1 (2+) 1824.3
    GTAAA 5′-5 756.5 (2+) 1511.0
    GTAA 5′-4 599.8 (2+) 1197.6
    AACGACGGCCAGT 13-3′ 1013.3 (4+), 1350.5 (3+) 4048.6
    ACGACGGCCAGT 12-3′ 1246.2 (3+) 3735.6
    CGACGGCCAGT 11-3′ 1141.7 (3+) 3422.1
    GACGGCCAGT 10-3′ 1045.4 (3+) 3133.2
    GGCCAGT 7-3′ 734.7 (2+) 2201.4
    CCAGT 5-3′ 772.5 (2+) 1543.0
    AGT 3-3′ 483.2 (2+), 965.3 (1+) 964.6
E9:DNase–Ni2+–ssDNA complexes
    E9:DNase-Ni2+-5-17-3 2548.1 (8+), 2265.1 (9+) 20 375.6
    E9:DNase-Ni2+-14-3 2440.0 (8+), 2169.0 (9+) 19 512.6
    E9:DNase-Ni2+-13-3 2400.9 (8+), 2134.3 (9+) 19 199.8
    E9:DNase-Ni2+-12-3 2361.5 (8+), 2099.2 (9+) 18 886.1
    E9:DNase-Ni2+-11-3 2322.6 (8+), 2064.6 (9+) 18 572.8

DNA fragments and non-covalent E9 DNase–Ni2+–ssDNA complexes resulting from the enzymatic reaction. E9 DNase (10 μM) was incubated with Ni2+ (20 μM) and 17mer ssDNA (100 μM) at 20°C for 45 min.