Metal-mediated DNA (mmDNA) presents a pathway toward
engineering
bioinorganic and electronic behavior into DNA devices. Many chemical
and biophysical forces drive the programmable chelation of metals
between pyrimidine base pairs. Here, we developed a crystallographic
method using the three-dimensional (3D) DNA tensegrity triangle motif
to capture single- and multi-metal binding modes across granular changes
to environmental pH using anomalous scattering. Leveraging this programmable
crystal, we determined 28 biomolecular structures to capture mmDNA
reactions. We found that silver(I) binds with increasing occupancy
in T–T and U–U pairs at elevated pH levels, and we exploited
this to capture silver(I) and mercury(II) within the same base pair
and to isolate the titration points for homo- and heterometal base
pair modes. We additionally determined the structure of a C–C
pair with both silver(I) and mercury(II). Finally, we extend our paradigm
to capture cadmium(II) in T–T pairs together with mercury(II)
at high pH. The precision self-assembly of heterobimetallic DNA chemistry
at the sub-nanometer scale will enable atomistic design frameworks
for more elaborate mmDNA-based nanodevices and nanotechnologies.