1hn3

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SOLUTION STRUCTURE OF THE N-TERMINAL 37 AMINO ACIDS OF THE MOUSE ARF TUMOR SUPPRESSOR PROTEIN

File:1hn3.gif


1hn3

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OverviewOverview

Arf is a tumor suppressor that regulates p53 function and is a frequent, target for loss in human cancers. Through two novel mechanisms, Arf, inhibits the oncoprotein Hdm2, a negative regulator of p53. (1) Arf, inhibits the E3 ubiquitin ligase activity of Hdm2 that leads to p53, degradation, and (2) Arf sequesters Hdm2 within nucleoli. These activities, of Arf promote p53-mediated cell cycle arrest and apoptosis. Fundamental, to these processes are interactions between Arf and Hdm2. Here we show, that a peptide containing the 37 N-terminal amino acids of mouse Arf, (mArfN37) localizes to nucleoli, sequesters Hdm2 within nucleoli, and, causes cell cycle arrest. Circular dichroism and NMR spectroscopy show, that mArfN37 is largely unstructured under aqueous conditions; however, the peptide adopts two alpha-helices (helix 1, residues 4-14; and helix 2, residues 20-29) in 2,2,2-trifluoroethanol (TFE). Each helix contains an, amino acid motif that is repeated twice in mArfN37, once in each helix., The two helices, however, do not interact but are connected by an, apparently flexible linker. The repeated motif contains Arg residues, spaced by a hydrophobic segment that may be involved in Hdm2 recognition, and binding. The RRPR nucleolar localization signal, contained within, residues 31-34, appears to be disordered under all conditions. The, identification of two Arf structural modules suggests that short peptides, containing the repeated motif may function as Arf mimics and may allow the, design of small molecule Arf mimics in the future.

About this StructureAbout this Structure

1HN3 is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.

ReferenceReference

Solution structure of the p53 regulatory domain of the p19Arf tumor suppressor protein., DiGiammarino EL, Filippov I, Weber JD, Bothner B, Kriwacki RW, Biochemistry. 2001 Feb 27;40(8):2379-86. PMID:11327858

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