LOCALIZATION OF THE BINDING REGION OF HIGH-MOBILITY GROUP PROTEIN-2 TO CISPLATIN-DAMAGED DNA

Citation
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
Citations number
35
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
268
Issue
32
Year of publication
1993
Pages
23940 - 23945
Database
ISI
SICI code
0021-9258(1993)268:32<23940:LOTBRO>2.0.ZU;2-Y
Abstract
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.