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Design of Inhibitors for S100B
Joseph Markowitz1, Alexander D Mackerell, France Carrier
1University of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, Maryland 21201, USA.
Abstract:
S100B interacts with the p53 protein in a calcium-dependent manner and down-regulates its function as a tumor suppressor. Therefore, inhibiting the S100B-p53 interaction represents a new approach for restoring functional wild-type p53 in cancers with elevated S100B such as found in malignant melanoma. A discussion of the biological rational for targeting S100B and a description of methodologies relevant to the discovery of compounds that inhibit S100B-p53 binding, including computational techniques, structural biology techniques, and cellular assays, is presented.

