Leyria Jimena, Fruttero Leonardo L, Ligabue-Braun Rodrigo, Defferrari Marina S, Arrese Estela L, Soulages José L, Settembrini Beatriz P, Carlini Celia R, Canavoso Lilián E
Departamento de Bioquímica Clínica-CIBICI-CONICET, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina.
Departamento de Bioquímica Clínica-CIBICI-CONICET, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Córdoba, Argentina; Brain Institute (Instituto do Cérebro-INSCER), Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.
J Insect Physiol. 2018 Feb-Mar;105:28-39. doi: 10.1016/j.jinsphys.2018.01.002. Epub 2018 Jan 8.
DmCatD, a cathepsin D-like peptidase of the hematophagous insect Dipetalogaster maxima, is synthesized by the fat body and the ovary and functions as yolk protein precursor. Functionally, DmCatD is involved in vitellin proteolysis. In this work, we purified and sequenced DmCatD, performed bioinformatic analyses and investigated the events involved in its targeting and storage in developing oocytes. By ion exchange and gel filtration chromatography, DmCatD was purified from egg homogenates and its identity was confirmed by mass spectrometry. Approximately 73% of the full-length transcript was sequenced. The phylogeny indicated that DmCatD has features which suggest its distancing from "classical" cathepsins D. Bioinformatic analyses using a chimeric construct were employed to predict post-translational modifications. Structural modeling showed that DmCatD exhibited the expected folding for this type of enzyme, and an active site with conserved architecture. The interaction between DmCatD and lipophorin in the hemolymph was demonstrated by co-immunoprecipitation. Colocalization of both proteins in developing oocyte membranes and yolk bodies was detected by immunofluorescence. Docking assays favoring the interaction DmCatD-lipophorin were carried out after modeling lipophorin of a related triatomine species. Our results suggest that lipophorin acts as a carrier for DmCatD to facilitate its further internalization by the oocytes. The mechanisms involved in the uptake of peptidases within the oocytes of insects have not been reported. This is the first experimental work supporting the interaction between cathepsin D and lipophorin in an insect species, enabling us to propose a pathway for its targeting and storage in developing oocytes.
DmCatD是吸血昆虫大斑长足蝽的一种组织蛋白酶D样肽酶,由脂肪体和卵巢合成,作为卵黄蛋白前体发挥作用。在功能上,DmCatD参与卵黄磷蛋白的蛋白水解。在这项研究中,我们对DmCatD进行了纯化和测序,进行了生物信息学分析,并研究了其在发育中的卵母细胞中靶向和储存所涉及的事件。通过离子交换和凝胶过滤色谱法,从卵匀浆中纯化出DmCatD,并通过质谱确认其身份。对全长转录本的约73%进行了测序。系统发育分析表明,DmCatD具有一些特征,表明它与“经典”组织蛋白酶D有所不同。使用嵌合构建体进行生物信息学分析以预测翻译后修饰。结构建模表明,DmCatD展现出这类酶预期的折叠结构,以及具有保守结构的活性位点。通过免疫共沉淀证明了DmCatD与血淋巴中的脂磷蛋白之间的相互作用。通过免疫荧光检测到这两种蛋白质在发育中的卵母细胞膜和卵黄小体中的共定位。在对相关锥蝽物种的脂磷蛋白进行建模后,进行了有利于DmCatD-脂磷蛋白相互作用的对接分析。我们的结果表明,脂磷蛋白作为DmCatD的载体,促进其被卵母细胞进一步内化。昆虫卵母细胞内肽酶摄取所涉及的机制尚未见报道。这是第一项支持昆虫物种中组织蛋白酶D与脂磷蛋白相互作用的实验研究,使我们能够提出其在发育中的卵母细胞中靶向和储存的途径。