Dl. Lawrence et al., LOCALIZATION OF THE BINDING REGION OF HIGH-MOBILITY GROUP PROTEIN-2 TO CISPLATIN-DAMAGED DNA, The Journal of biological chemistry, 268(32), 1993, pp. 23940-23945
Cisplatin (CDDP) is an effective cancer chemotherapeutic drug used in
the treatment of several human malignancies. The effectiveness of cisp
latin therapy is limited by intrinsic resistance of tumors to this dru
g as well as the development of secondary tumors, which are also drug
resistant. A potential mechanism influencing the sensitivity of cells
to CDDP may result from the interaction of specific proteins with CDDP
-damaged DNA (CDDP-DNA). In an earlier report, we demonstrated that hi
gh mobility group (HMG) proteins 1 and 2 bind with high affinity to CD
DP-DNA. In the present study partial proteolytic digestion was used to
localize the binding region of HMG2. A proteolytic fragment of approx
imately 20 kDa, containing the amino-terminal region of the protein, m
aintains the ability to bind with high affinity to CDDP-DNA, while an
amino-terminal fragment of 14 kDa binds with slightly reduced affinity
. In contrast, a peptide fragment lacking 51 NH2-terminal amino acids
from HMG2 has greatly reduced affinity for damaged DNA. Recombinant pe
ptide fragments containing HMG box-1 or HMG box 2 bind weakly to damag
ed DNA, while a recombinant fragment containing HMG boxes 1 and 2 bind
s with high affinity. Hence, our results indicate that the amino-termi
nal region of HMG2 contains the damaged DNA binding recognition site a
nd that both HMG boxes 1 and 2, present in the parental molecule, are
required for high affinity binding of this protein to CDDP-DNA.