首页> 美国卫生研究院文献>Journal of Virology >Interaction of Autographa californica Multiple Nucleopolyhedrovirus Cathepsin Protease Progenitor (proV-CATH) with Insect Baculovirus Chitinase as a Mechanism for proV-CATH Cellular Retention
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Interaction of Autographa californica Multiple Nucleopolyhedrovirus Cathepsin Protease Progenitor (proV-CATH) with Insect Baculovirus Chitinase as a Mechanism for proV-CATH Cellular Retention

机译:加利福尼亚州卷柏多核多角体病毒组织蛋白酶蛋白酶祖细胞(proV-CATH)与昆虫杆状病毒几丁质酶的相互作用作为proV-CATH细胞保留的机制。

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摘要

The insect baculovirus chitinase (CHIA) and cathepsin protease (V-CATH) enzymes cause terminal host insect liquefaction, enhancing the dissemination of progeny virions away from the host cadavers. Regulated and delayed cellular release of these host tissue-degrading enzymes ensures that liquefaction starts only after optimal viral replication has occurred. Baculoviral CHIA remains intracellular due to its C-terminal KDEL endoplasmic reticulum (ER) retention motif. However, the mechanism for cellular retention of the inactive V-CATH progenitor (proV-CATH) has not yet been determined. Signal peptide cleavage occurs upon cotranslational ER import of the v-cath-expressed protein, and ER-resident CHIA is needed for the folding of proV-CATH. Although this implies that CHIA and proV-CATH bind each other in the ER, the putative CHIA–proV-CATH interaction has not been experimentally verified. We demonstrate that the amino-terminal 22 amino acids (aa) of Autographa californica multiple nucleopolyhedrovirus (AcMNPV) preproV-CATH are responsible for the entry of proV-CATH into the ER. Furthermore, the CHIA–green fluorescent protein (GFP) and proV-CATH-red fluorescent protein (RFP) fusion proteins colocalize in the ER. Using monomeric RFP (mRFP)-based bimolecular fluorescence complementation (BiFC), we determined that CHIA and proV-CATH interact directly with each other in the ER during virus replication. Moreover, reciprocal Ni/His pulldowns of His-tagged proteins confirmed the CHIA–proV-CATH interaction biochemically. The reciprocal copurification of CHIA and proV-CATH suggests a specific CHIA–proV-CATH interaction and corroborates our BiFC data. Deletion of the CHIA KDEL motif allowed for premature CHIA secretion from cells, and proV-CATH was similarly prematurely secreted from cells along with ΔKDEL-CHIA. These data suggest that CHIA and proV-CATH interact directly with each other and that this interaction aids the cellular retention of proV-CATH.
机译:昆虫杆状病毒几丁质酶(CHIA)和组织蛋白酶蛋白酶(V-CATH)引起宿主宿主昆虫液化,从而增强了子代病毒体从宿主尸体的传播。这些宿主组织降解酶的调节和延迟细胞释放确保液化仅在发生最佳病毒复制后才开始。杆状病毒CHIA由于其C端KDEL内质网(ER)保留基序而保留在细胞内。但是,尚未确定非活性V-CATH祖细胞(proV-CATH)的细胞保留机制。信号肽的裂解发生在v-cath表达的蛋白质的共翻译ER导入时,并且ProV-CATH折叠需要ER驻留的CHIA。尽管这意味着CHIA和proV-CATH在ER中相互结合,但是尚未通过实验验证推定的CHIA-proV-CATH相互作用。我们证明,Autographa californica多核多角体病毒(AcMNPV)preproV-CATH的氨基末端22个氨基酸(aa)负责proV-CATH进入ER。此外,CHIA绿色荧光蛋白(GFP)和proV-CATH红色荧光蛋白(RFP)融合蛋白在ER中共定位。使用基于单体RFP(mRFP)的双分子荧光互补(BiFC),我们确定CHIA和proV-CATH在病毒复制过程中在ER中彼此直接相互作用。此外,His标记蛋白的互逆Ni / His下拉在生化方面证实了CHIA-proV-CATH的相互作用。 CHIA和proV-CATH的相互共纯化表明了CHIA-proV-CATH的特定相互作用,并证实了我们的BiFC数据。 CHIA KDEL基序的删除允许从细胞中过早地分泌出CHIA,类似地,proV-CATH与ΔKDEL-CHIA一起过早地从细胞中分泌出来。这些数据表明CHIA和proV-CATH直接直接相互作用,并且这种相互作用有助于proV-CATH的细胞保留。

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