Ylilauri, Mikko; Mattila, Elina; Nurminen, Elisa M.; Kapyla, Jarmo; Niinivehmas, Sanna P.; Maatta, Juha A.; Pentikainen, Ulla; Ivaska, Johanna; Pentikainen, Olli T.
Molecular mechanism of T-cell protein tyrosine phosphatase (TCPTP) activation by mitoxantrone
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 1834:1988-1997, OCT 2013

T-cell protein tyrosine phosphatase (TCPTP) is a ubiquitously expressed non-receptor protein tyrosine phosphatase. It is involved in the negative regulation of many cellular signaling pathways. Thus, activation of TCPTP could have important therapeutic applications in diseases such as cancer and inflammation. We have previously shown that the alpha-cytoplasmic tail of integrin alpha(1)beta(1) directly binds and activates TCPTP. In addition, we have identified in a large-scale high-throughput screen six small molecules that activate TCPTP. These small molecule activators include mitoxantrone and spermidine. In this study, we have investigated the molecular mechanism behind agonist-induced TCPTP activation. By combining several molecular modeling and biochemical techniques, we demonstrate that alpha(1)-peptide and mitoxantrone activate TCPTP via direct binding to the catalytic domain, whereas spermidine does not interact with the catalytic domain of TCPTP in vitro. Furthermore, we have identified a hydrophobic groove surrounded by negatively charged residues on the surface of TCPTP as a putative binding site for the alpha(1)-peptide and mitoxantrone. Importantly, these data have allowed us to identify a new molecule that binds to TCPTP, but interestingly cannot activate its phosphatase activity. Accordingly, we describe here mechanism of TCPTP activation by mitoxantrone, the cytoplasmic tail of alpha(1)-integrin, and a mitoxantrone-like molecule at the atomic level. These data provide invaluable insight into the development of novel TCPTP activators, and may facilitate the rational discovery of small-molecule cancer therapeutics. (C) 2013 Elsevier B.V. All rights reserved.

DOI:10.1016/j.bbapap.2013.07.001

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