%0 Journal Article
%T Phosphorylation and Methylation of Proteasomal Proteins of the Haloarcheon Haloferax volcanii
%A Matthew A. Humbard
%A Christopher J. Reuter
%A Kheir Zuobi-Hasona
%A Guangyin Zhou
%A Julie A. Maupin-Furlow
%J Archaea
%D 2010
%I Hindawi Publishing Corporation
%R 10.1155/2010/481725
%X Proteasomes are composed of 20S core particles (CPs) of - and -type subunits that associate with regulatory particle AAA ATPases such as the proteasome-activating nucleotidase (PAN) complexes of archaea. In this study, the roles and additional sites of post-translational modification of proteasomes were investigated using the archaeon Haloferax volcanii as a model. Indicative of phosphorylation, phosphatase-sensitive isoforms of 1 and 2 were detected by 2-DE immunoblot. To map these and other potential sites of post-translational modification, proteasomes were purified and analyzed by tandem mass spectrometry (MS/MS). Using this approach, several phosphosites were mapped including 1 Thr147, 2 Thr13/Ser14 and PAN-A Ser340. Multiple methylation sites were also mapped to 1, thus, revealing a new type of proteasomal modification. Probing the biological role of 1 and PAN-A phosphorylation by site-directed mutagenesis revealed dominant negative phenotypes for cell viability and/or pigmentation for 1 variants including Thr147Ala, Thr158Ala and Ser58Ala. An H. volcanii Rio1p Ser/Thr kinase homolog was purified and shown to catalyze autophosphorylation and phosphotransfer to 1. The 1 variants in Thr and Ser residues that displayed dominant negative phenotypes were significantly reduced in their ability to accept phosphoryl groups from Rio1p, thus, providing an important link between cell physiology and proteasomal phosphorylation.
%U http://www.hindawi.com/journals/arch/2010/481725/