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恶性疟原虫:印度分离株野外样本中裂殖子表面蛋白-1 C 端富含半胱氨酸区域的变异

Plasmodium falciparum: variations in the C-terminal cysteine-rich region of the merozoite surface protein-1 in field samples among Indian isolates.

作者信息

Lalitha P V, Malhotra P, Chattopadhyay R, Chauhan V S

机构信息

International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, 110067, India.

出版信息

Exp Parasitol. 1999 May;92(1):12-8. doi: 10.1006/expr.1999.4401.

Abstract

The cysteine-rich C-terminal region of the merozoite surface protein-1, MSP-119, of Plasmodium falciparum has been the most promising vaccine target antigen to date, based on protective immunization studies with recombinant proteins in mice and monkey models. To be further developed as a vaccine candidate, it is essential to study its sequence heterogeneity in field isolates from diverse geographical areas. We have analyzed the DNA sequences encoding the C-terminal region of P. falciparum MSP-1 (1526-1744 aa, corresponding to part of the 16th and all of the 17th blocks) of 16 isolates from different regions in India. The PNG-MAD20 type of MSP-1 sequence predominated in this subcontinent. The MSP-119 region as usual was found to be highly conserved, with amino acid variations at four positions. Based on these variations, only three MSP-119 forms (Q-KNG, E-KNG, and E-TSG, a novel variant) were detected among these isolates. The two MSP-119 variant forms (Q-KNG and E-TSG) were expressed in Escherichia coli as histidine-tagged polypeptides and were characterized immunologically to corroborate the sequence data.

摘要

基于在小鼠和猴模型中使用重组蛋白进行的保护性免疫研究,恶性疟原虫裂殖子表面蛋白1(MSP-1)富含半胱氨酸的C末端区域MSP-119,是迄今为止最有前景的疫苗靶抗原。要进一步开发成为候选疫苗,研究其在不同地理区域的野外分离株中的序列异质性至关重要。我们分析了来自印度不同地区的16株分离株中编码恶性疟原虫MSP-1 C末端区域(1526-1744氨基酸,对应于第16部分和第17部分全部)的DNA序列。在该次大陆,MSP-1序列的PNG-MAD20类型占主导地位。如往常一样,发现MSP-119区域高度保守,在四个位置存在氨基酸变异。基于这些变异,在这些分离株中仅检测到三种MSP-119形式(Q-KNG、E-KNG和E-TSG,一种新变体)。两种MSP-119变体形式(Q-KNG和E-TSG)在大肠杆菌中作为组氨酸标签多肽表达,并进行了免疫学表征以证实序列数据。

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