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首页> 外文期刊>Expert review of proteomics >Quantitative proteomic analysis of venom from Southern India common krait (Bungarus caeruleus) and identification of poorly immunogenic toxins by immune-profiling against commercial antivenom
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Quantitative proteomic analysis of venom from Southern India common krait (Bungarus caeruleus) and identification of poorly immunogenic toxins by immune-profiling against commercial antivenom

机译:来自印度南部的毒液的定量蛋白质组学分析常见的KRAIT(BUNGARUS caeruleus)和商业抗静电型免疫分析鉴定免疫原毒素

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Objectives: To study the venom proteome composition of Southern India (SI) Common Krait (Bungarus caeruleus) and immunological cross-reactivity between venom against commercial antivenom.Methods: Proteomic analysis was done by nano LC-MS/MS and toxins were quantitated by label-free analysis. The immunological cross-reactivity of venom towards polyvalent antivenom (PAV) was assessed by ELISA, Immunoblotting, and immuno-chromatographic methods.Results: A total of 57 enzymatic and non-enzymatic proteins belonging to 12 snake venom protein families were identified. The three finger toxins (3FTx) (48.3%) and phospholipase A(2) (PLA(2)) (37.6%) represented the most abundant non-enzymatic and enzymatic proteins, respectively. -bungarotoxin (12.9%), a presynaptic neurotoxin, was also identified. The venom proteome composition is well correlated with its enzymatic activities, reported pharmacological properties, and clinical manifestations of krait envenomation. Immuno-cross-reactivity studies demonstrated better recognition of high molecular weight proteins (>45 kDa) of this venom by PAVs compared to low molecular weight (<15 kDa) toxins such as PLA(2) and 3FTxs.Conclusion: The poor recognition of <15 kDa mass SI B. caeruleus venom proteins is of grave concern for the successful treatment of krait envenomation. Therefore, emphasis should be given to improve the immunization protocols and/or supplement of antibodies raised specifically against the <15 kDa toxins of this venom.
机译:目标:研究印度南部的毒液蛋白质组成(Si)常见的KRAIT(BUNGARUS CAERULEUS)和毒液之间的免疫交叉反应性。方法:蛋白质组学分析通过纳米LC-MS / MS和毒素通过标记定量 - 免费分析。通过ELISA,免疫印迹和免疫色谱法评估毒液朝向多价抗静电(PAV)的免疫交叉反应性。结果:确定了属于12个蛇毒液蛋白质家族的57个酶和非酶促蛋白。三指毒素(3FRX)(48.3%)和磷脂酶A(2)(PLA(2))(37.6%)分别代表了最丰富的非酶促和酶蛋白。 -Bungarotoxin(12.9%)也鉴定出突触前神经毒素。毒液蛋白质组合物与其酶活性,报告的药理学性质以及Krait Envenomation的临床表现良好。免疫交叉反应性研究通过PAV与PLA(2)和3ftxs等低分子量(<15kDa)毒素相比,通过Pavs更好地识别该毒液的高分子量蛋白(> 45kDa)。结论:识别差<15 kda mass si b. caeruleus毒液蛋白对Krait Envenomation的成功治疗非常关注。因此,应强调改善抗体的免疫方案和/或补充特别针对该毒液<15kDa毒素的抗体。

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