Kuroyanagi Miwa, Nishimura Mikio, Hara-Nishimura Ikuko
Department of Botany, Graduate School of Science, Kyoto University, Kyoto, 606--8502 Japan.
Plant Cell Physiol. 2002 Feb;43(2):143-51. doi: 10.1093/pcp/pcf035.
Vacuolar processing enzyme (VPE) is a cysteine proteinase responsible for the maturation of various vacuolar proteins in higher plants. To clarify the mechanism of maturation and activation of VPE, we expressed the precursors of Arabidopsis gamma VPE in insect cells. The cells accumulated a glycosylated proprotein precursor (pVPE) and an unglycosylated preproprotein precursor (ppVPE) which might be unfolded. The N-terminal sequence of pVPE revealed that ppVPE had a 22-amino-acid signal peptide to be removed co-translationally. Under acidic conditions, the 56-kDa pVPE was self-catalytically converted to a 43-kDa intermediate form (iVPE) and then to the 40-kDa mature form (mVPE). N-terminal sequencing of iVPE and mVPE showed that sequential removal of the C-terminal propeptide and N-terminal propeptide produced mVPE. Both iVPE and mVPE exhibited the activity, while pVPE exhibited no activity. These results imply that the removal of the C-terminal propeptide is essential for activating the enzyme. Further removal of the N-terminal propeptide from iVPE is not required to activate the enzyme. To demonstrate that the C-terminal propeptide functions as an inhibitor of VPE, we expressed the C-terminal propeptide and produced specific antibodies against it. We found that the C-terminal propeptide reduced the activity of VPE and that this inhibitory activity was suppressed by specific antibodies against it. Our findings suggest that the C-terminal propeptide functions as an auto-inhibitory domain that masks the catalytic site. Thus, the removal of the C-terminal propeptide of pVPE might expose the catalytic site of the enzyme.
液泡加工酶(VPE)是一种半胱氨酸蛋白酶,负责高等植物中各种液泡蛋白的成熟。为了阐明VPE成熟和激活的机制,我们在昆虫细胞中表达了拟南芥γVPE的前体。细胞积累了一种糖基化的前体蛋白前体(pVPE)和一种可能未折叠的非糖基化前原蛋白前体(ppVPE)。pVPE的N端序列显示,ppVPE有一个22个氨基酸的信号肽,可在共翻译时被去除。在酸性条件下,56 kDa的pVPE自催化转化为43 kDa的中间形式(iVPE),然后再转化为40 kDa的成熟形式(mVPE)。iVPE和mVPE的N端测序表明,C端前肽和N端前肽的顺序去除产生了mVPE。iVPE和mVPE均表现出活性,而pVPE没有活性。这些结果表明,C端前肽的去除对于激活该酶至关重要。从iVPE中进一步去除N端前肽对于激活该酶不是必需的。为了证明C端前肽作为VPE的抑制剂发挥作用,我们表达了C端前肽并产生了针对它的特异性抗体。我们发现C端前肽降低了VPE的活性,并且这种抑制活性被针对它的特异性抗体所抑制。我们的研究结果表明,C端前肽作为一个自抑制结构域,掩盖了催化位点。因此,pVPE的C端前肽的去除可能会暴露该酶的催化位点。