Laboratório de Biologia Molecular e Doenças Endêmicas, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Parasit Vectors. 2012 Jun 20;5:123. doi: 10.1186/1756-3305-5-123.
The mosquito Culex quinquefasciatu s, a widespread insect in tropical and sub-tropical regions of the world, is a vector of multiple arboviruses and parasites, and is considered an important risk to human and veterinary health. Proteolytic enzymes play crucial roles in the insect physiology including the modulation of embryonic development and food digestion. Therefore, these enzymes represent important targets for the development of new control strategies. This study presents zymographic characterization and comparative analysis of the proteolytic activity found in eggs, larval instars and pupae of Culex quinquefasciatus.
The proteolytic profiles of eggs, larvae and pupa of Cx. quinquefasciatus were characterized by SDS-PAGE co-polymerized with 0.1% gelatin, according to the pH, temperature and peptidase inhibitor sensitivity. In addition, the proteolytic activities were characterized in solution using 100 μM of the fluorogenic substrate Z-Phe-Arg-AMC.
Comparison of the proteolytic profiles by substrate-SDS-PAGE from all preimaginal stages of the insect revealed qualitative and quantitative differences in the peptidase expression among eggs, larvae and pupae. Use of specific inhibitors revealed that the proteolytic activity from preimaginal stages is mostly due to trypsin-like serine peptidases that display optimal activity at alkaline pH. In-solution, proteolytic assays of the four larval instars using the fluorogenic substrate Z-Phe-Arg-AMC in the presence or absence of a trypsin-like serine peptidase inhibitor confirmed the results obtained by substrate-SDS-PAGE analysis. The trypsin-like serine peptidases of the four larval instars were functional over a wide range of temperatures, showing activities at 25°C and 65°C, with an optimal activity between 37°C and 50°C.
The combined use of zymography and in-solution assays, as performed in this study, allowed for a more detailed analysis of the repertoire of proteolytic enzymes in preimaginal stages of the insect. Finally, differences in the trypsin-like serine peptidase profile of preimaginal stages were observed, suggesting that such enzymes exert specific functions during the different stages of the life cycle of the insect.
蚊子 Culex quinquefasciatu s 广泛分布于世界热带和亚热带地区,是多种虫媒病毒和寄生虫的载体,被认为是人类和兽医健康的重要风险因素。蛋白水解酶在昆虫生理中起着至关重要的作用,包括调节胚胎发育和食物消化。因此,这些酶是开发新控制策略的重要目标。本研究介绍了 Culex quinquefasciatus 卵、幼虫和蛹中发现的蛋白水解活性的酶谱特征和比较分析。
采用 SDS-PAGE 共聚合 0.1%明胶的方法,根据 pH 值、温度和肽酶抑制剂敏感性,对 Cx. quinquefasciatus 卵、幼虫和蛹的蛋白水解谱进行了特征描述。此外,还使用 100 μM 的荧光底物 Z-Phe-Arg-AMC 在溶液中对蛋白水解活性进行了特征描述。
对昆虫所有预成虫阶段的底物-SDS-PAGE 蛋白水解谱进行比较,发现卵、幼虫和蛹中肽酶表达存在定性和定量差异。使用特异性抑制剂表明,预成虫阶段的蛋白水解活性主要来自胰凝乳蛋白酶样丝氨酸肽酶,其在碱性 pH 值下显示最佳活性。在溶液中,使用荧光底物 Z-Phe-Arg-AMC 对四个幼虫龄期进行的蛋白水解测定,在存在或不存在胰凝乳蛋白酶样丝氨酸肽酶抑制剂的情况下,证实了底物-SDS-PAGE 分析的结果。四个幼虫龄期的胰凝乳蛋白酶样丝氨酸肽酶在较宽的温度范围内具有功能,在 25°C 和 65°C 下具有活性,在 37°C 至 50°C 之间具有最佳活性。
本研究中采用的酶谱和溶液分析相结合的方法,使我们能够更详细地分析昆虫预成虫阶段蛋白水解酶的酶谱。最后,观察到预成虫阶段胰凝乳蛋白酶样丝氨酸肽酶谱存在差异,表明这些酶在昆虫生命周期的不同阶段发挥特定功能。