When sprayed from physiological ionic strength, nucleic acids typically end up with low levels of charging and in compact conformations. Increasing the electrospray negative charging of nucleic acids while preserving the native noncovalent interactions can help distinguish solution folds by ion mobility mass spectrometry. To get fundamental insight into the supercharging mechanisms of nucleic acids in the negative mode, we studied model G-quadruplex structures and single-strand controls in 100 mM ammonium acetate. We found that adding 0.4% of propylene carbonate, 0.4% of sulfolane, or 0.1% of m -NBA induces native supercharging. However, although 0.4% of m -NBA shows the highest supercharging ability, it induces unwanted unfolding of solution-folded G-quadruplexes. The supercharging effect resembles the effect of lowering the ionic strength, and this could be explained by partial neutralization of the ampholytes when droplets become more concentrated in their nonaqueous components. The supercharging ability ranks PC < sulfolane < m -NBA. m -NBA adducts to G-quadruplexes with high-charge states confirm that the supercharging agent interacts directly with DNA. Surprisingly, in the presence of supercharging agents, the most negatively-charged states also bear more alkali metal ion adducts. Larger droplets are known to result in more counterion adduction, so our results are consistent with native supercharging conditions producing larger droplets evaporating to a charged residue. However, when negative charge carriers from the electrolyte become too rare, chain ejection accompanied by denaturation, and hence non-native supercharging, can become predominant.