Richards Elaine H, Dani M Paulina
Central Science Laboratory, Sand Hutton, York Y041 1LZ, UK.
J Insect Physiol. 2008 Jun;54(6):1041-9. doi: 10.1016/j.jinsphys.2008.04.003. Epub 2008 Apr 11.
Pimpla hypochondriaca venom is complex and contains a number of different proteins and polypeptides that exert a variety of effects on insect physiology. In particular, it possesses factors with potent anti-haemocyte and immunosuppressive properties. In the current work, we describe the biochemical isolation of a single venom factor with insect haemocyte anti-aggregation properties. The protein was isolated using gel filtration and ion exchange chromatography, in conjunction with a qualitative in vitro haemocyte anti-aggregation assay to monitor activity and confirm identity. The protein has a molecular weight estimate of 33kDa (determined by SDS PAGE under reducing conditions), and an N-terminal sequence of Asp-Ser-Asp-Ile-Tyr-Leu-Leu. The biochemically isolated protein has been demonstrated to inhibit haemocyte aggregation and to suppress encapsulation responses, using in vitro and in vivo assays, respectively. Furthermore, its gene has been identified as vpr3. The work is presented within the context of the role of P. hypochondriaca venom and the isolated protein in host immune suppression.
拟寄蝇毒液成分复杂,含有多种不同的蛋白质和多肽,这些成分对昆虫生理机能具有多种影响。特别是,它含有具有强大抗血细胞和免疫抑制特性的因子。在当前的研究中,我们描述了一种具有昆虫血细胞抗聚集特性的单一毒液因子的生化分离过程。该蛋白质通过凝胶过滤和离子交换色谱法进行分离,并结合定性体外血细胞抗聚集试验来监测活性并确认其身份。该蛋白质的分子量估计为33kDa(在还原条件下通过SDS-PAGE测定),N端序列为Asp-Ser-Asp-Ile-Tyr-Leu-Leu。分别通过体外和体内试验证明,这种生化分离得到的蛋白质能够抑制血细胞聚集并抑制包囊反应。此外,其基因已被鉴定为vpr3。本文在拟寄蝇毒液及分离出的蛋白质在宿主免疫抑制中的作用背景下展开论述。