Table 1.

List of DNA sequences used in this study, Myb397–415-induced thermal stabilization (ΔT1/2) for G4 and duplex DNA structures measured by CD melting experiments, and equilibrium dissociation constants (Kd) for the binding of Myb397–415 to DNAs obtained by MST experiments

DNASequence (5′ → 3′)StructureΔT1/2(°C)aKd(nM)
c-KIT1AGGGAGGGCGCTGGGAGGAGGGparallel G46.2 (±0.2)340 (±44)
c-KIT2CGGGCGGGCGCTAGGGAGGGTparallel G411.2 (±0.2)130 (±15)
c-MYCTGAGGGTGGGTAGGGTGGGTAAparallel G45.0 (±0.2)430 (±100)
HER2GGAGAAGGAGGAGGTGGAGGAGGAGGGparallel G47.0 (±0.2)130 (±20)
HT-FANATAGGGTTAGGGTTAGGGTTAGGGbparallel G48.3 (±0.2)140 (±26)
HRAS1TCGGGTTGCGGGCGCAGGGCACGGGCGantiparallel G4–2.0 (±0.2)n.d.c
LWDLN1GGGTTTGGGTTTTGGGAGGGantiparallel G4–4.0 (±0.2)n.d.c
BCL-2GGGCGCGGGAGGAATTGGGCGGGhybrid G48.0 (±0.2)280 (±42)
HT1TTGGGTTAGGGTTAGGGTTAGGGAhybrid G41.6 (±0.2)900 (±140)
HT2TTAGGGTTAGGGTTAGGGTTAGGGTThybrid G42.7 (±0.2)1180 (±90)
VEGFR-17TGGGTACCCGGGTGAGGTGCGGGGThybrid G40.2 (±0.2)n.d.c
ds12CGCGAATTCGCGduplex1.0 (±0.2)n.d.c
DNASequence (5′ → 3′)StructureΔT1/2(°C)aKd(nM)
c-KIT1AGGGAGGGCGCTGGGAGGAGGGparallel G46.2 (±0.2)340 (±44)
c-KIT2CGGGCGGGCGCTAGGGAGGGTparallel G411.2 (±0.2)130 (±15)
c-MYCTGAGGGTGGGTAGGGTGGGTAAparallel G45.0 (±0.2)430 (±100)
HER2GGAGAAGGAGGAGGTGGAGGAGGAGGGparallel G47.0 (±0.2)130 (±20)
HT-FANATAGGGTTAGGGTTAGGGTTAGGGbparallel G48.3 (±0.2)140 (±26)
HRAS1TCGGGTTGCGGGCGCAGGGCACGGGCGantiparallel G4–2.0 (±0.2)n.d.c
LWDLN1GGGTTTGGGTTTTGGGAGGGantiparallel G4–4.0 (±0.2)n.d.c
BCL-2GGGCGCGGGAGGAATTGGGCGGGhybrid G48.0 (±0.2)280 (±42)
HT1TTGGGTTAGGGTTAGGGTTAGGGAhybrid G41.6 (±0.2)900 (±140)
HT2TTAGGGTTAGGGTTAGGGTTAGGGTThybrid G42.7 (±0.2)1180 (±90)
VEGFR-17TGGGTACCCGGGTGAGGTGCGGGGThybrid G40.2 (±0.2)n.d.c
ds12CGCGAATTCGCGduplex1.0 (±0.2)n.d.c

aΔT1/2 represents the difference in melting temperature [ΔT1/2T1/2 (DNA + peptide) – T1/2 (DNA)]. The T1/2 values of DNA alone are: c-KIT1 = 53.8 (±0.1)°C, c-KIT2 = 59.5 (±0.1)°C, c-MYC= 68.2 (±0.1)°C, HER2 = 62.4 (±0.1)°C, HT-FANA = 62.9 (±0.1)°C, HRAS1 = 52.3 (±0.1)°C, LWDLN1 = 49.6 (±0.1)°C, BCL-2 = 60.7 (±0.1)°C, HT1 = 56.9 (±0.1)°C, HT2 = 42.7 (±0.1)°C, VEGFR-17T = 53.7 (±0.1)°C, ds12 = 62.7 (±0.1)°C. bBold G denotes 2′-fluoroarabino-guanosine (2′-F-ANA-guanosine). cn.d. = not determined due to undetectable binding.

Table 1.

List of DNA sequences used in this study, Myb397–415-induced thermal stabilization (ΔT1/2) for G4 and duplex DNA structures measured by CD melting experiments, and equilibrium dissociation constants (Kd) for the binding of Myb397–415 to DNAs obtained by MST experiments

DNASequence (5′ → 3′)StructureΔT1/2(°C)aKd(nM)
c-KIT1AGGGAGGGCGCTGGGAGGAGGGparallel G46.2 (±0.2)340 (±44)
c-KIT2CGGGCGGGCGCTAGGGAGGGTparallel G411.2 (±0.2)130 (±15)
c-MYCTGAGGGTGGGTAGGGTGGGTAAparallel G45.0 (±0.2)430 (±100)
HER2GGAGAAGGAGGAGGTGGAGGAGGAGGGparallel G47.0 (±0.2)130 (±20)
HT-FANATAGGGTTAGGGTTAGGGTTAGGGbparallel G48.3 (±0.2)140 (±26)
HRAS1TCGGGTTGCGGGCGCAGGGCACGGGCGantiparallel G4–2.0 (±0.2)n.d.c
LWDLN1GGGTTTGGGTTTTGGGAGGGantiparallel G4–4.0 (±0.2)n.d.c
BCL-2GGGCGCGGGAGGAATTGGGCGGGhybrid G48.0 (±0.2)280 (±42)
HT1TTGGGTTAGGGTTAGGGTTAGGGAhybrid G41.6 (±0.2)900 (±140)
HT2TTAGGGTTAGGGTTAGGGTTAGGGTThybrid G42.7 (±0.2)1180 (±90)
VEGFR-17TGGGTACCCGGGTGAGGTGCGGGGThybrid G40.2 (±0.2)n.d.c
ds12CGCGAATTCGCGduplex1.0 (±0.2)n.d.c
DNASequence (5′ → 3′)StructureΔT1/2(°C)aKd(nM)
c-KIT1AGGGAGGGCGCTGGGAGGAGGGparallel G46.2 (±0.2)340 (±44)
c-KIT2CGGGCGGGCGCTAGGGAGGGTparallel G411.2 (±0.2)130 (±15)
c-MYCTGAGGGTGGGTAGGGTGGGTAAparallel G45.0 (±0.2)430 (±100)
HER2GGAGAAGGAGGAGGTGGAGGAGGAGGGparallel G47.0 (±0.2)130 (±20)
HT-FANATAGGGTTAGGGTTAGGGTTAGGGbparallel G48.3 (±0.2)140 (±26)
HRAS1TCGGGTTGCGGGCGCAGGGCACGGGCGantiparallel G4–2.0 (±0.2)n.d.c
LWDLN1GGGTTTGGGTTTTGGGAGGGantiparallel G4–4.0 (±0.2)n.d.c
BCL-2GGGCGCGGGAGGAATTGGGCGGGhybrid G48.0 (±0.2)280 (±42)
HT1TTGGGTTAGGGTTAGGGTTAGGGAhybrid G41.6 (±0.2)900 (±140)
HT2TTAGGGTTAGGGTTAGGGTTAGGGTThybrid G42.7 (±0.2)1180 (±90)
VEGFR-17TGGGTACCCGGGTGAGGTGCGGGGThybrid G40.2 (±0.2)n.d.c
ds12CGCGAATTCGCGduplex1.0 (±0.2)n.d.c

aΔT1/2 represents the difference in melting temperature [ΔT1/2T1/2 (DNA + peptide) – T1/2 (DNA)]. The T1/2 values of DNA alone are: c-KIT1 = 53.8 (±0.1)°C, c-KIT2 = 59.5 (±0.1)°C, c-MYC= 68.2 (±0.1)°C, HER2 = 62.4 (±0.1)°C, HT-FANA = 62.9 (±0.1)°C, HRAS1 = 52.3 (±0.1)°C, LWDLN1 = 49.6 (±0.1)°C, BCL-2 = 60.7 (±0.1)°C, HT1 = 56.9 (±0.1)°C, HT2 = 42.7 (±0.1)°C, VEGFR-17T = 53.7 (±0.1)°C, ds12 = 62.7 (±0.1)°C. bBold G denotes 2′-fluoroarabino-guanosine (2′-F-ANA-guanosine). cn.d. = not determined due to undetectable binding.

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