Multiple modes of interaction of the deglycosylation enzyme, mouse peptide
            <i>N</i>
            -glycanase, with the proteasome

Guangtao Li, Xiaoke Zhou, Gang Zhao, Hermann Schindelin, William J. Lennarz

doi:10.1073/pnas.0507155102

<jats:p> Peptide <jats:italic>N</jats:italic> -glycanase (PNGase) is involved in the cleavage of oligosaccharide chains from misfolded glycoproteins that are destined for degradation by the proteasome. Earlier, a number of potential binding partners of mouse PNGase (mPNGase) were detected by using the yeast two-hybrid system. In the current study, an <jats:italic>in vitro</jats:italic> system was set up to investigate direct interactions between mPNGase and these candidate proteins. Although the yeast two-hybrid system suggested an interaction of six different proteins with mPNGase, only mHR23B and the proteasome subunit mS4 were found to interact with mPNGase. In fact, mS4 competes with mHR23B for binding to mPNGase. These results suggested two possible pathways for the interaction between mPNGase and the proteasome. In one pathway, mHR23B mediates the interaction between mPNGase and the proteasome. In an alternative pathway, mPNGase directly binds to the proteasome subunit, mS4. In either case, it is clear that PNGase is located in close proximity to the proteasome and is available for deglycosylation of glycoproteins destined for degradation. Surprisingly, mPNGase also was found to mediate binding of the cytoplasmic protein, p97, to the proteasome through the formation of a ternary complex made up of mHR23B, mPNGase, and p97. Because p97 is known to bind to the endoplasmic reticulum membrane protein AMFR (gp78), an E3 ligase, we propose a model in which p97, mPNGase, and mHR23B mediate interaction of the endoplasmic reticulum with the proteasome. </jats:p>

Multiple modes of interaction of the deglycosylation enzyme, mouse peptide <i>N</i> -glycanase, with the proteasome

抄録

収録刊行物

被引用文献 (6)*注記

キーワード

詳細情報詳細情報について

書き出し

問題の指摘