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恶性疟原虫裂殖子表面蛋白复合物的22 kDa组分源自一种更大的前体,即裂殖子表面蛋白7。

The 22 kDa component of the protein complex on the surface of Plasmodium falciparum merozoites is derived from a larger precursor, merozoite surface protein 7.

作者信息

Pachebat J A, Ling I T, Grainger M, Trucco C, Howell S, Fernandez-Reyes D, Gunaratne R, Holder A A

机构信息

Division of Parasitology, National Institute for Medical Research, Mill Hill, NW7 1AA, London, UK.

出版信息

Mol Biochem Parasitol. 2001 Sep 28;117(1):83-9. doi: 10.1016/s0166-6851(01)00336-x.

Abstract

The gene coding for merozoite surface protein 7 has been identified and sequenced in three lines of Plasmodium falciparum. The gene encodes a 351 amino acid polypeptide that is the precursor of a 22-kDa protein (MSP7(22)) on the merozoite surface and non-covalently associated with merozoite surface protein 1 (MSP1) complex shed from the surface at erythrocyte invasion. A second 19-kDa component of the complex (MSP7(19)) was shown to be derived from MSP7(22) and the complete primary structure of this polypeptide was confirmed by mass spectrometry. The protein sequence contains several predicted helical and two beta elements, but has no similarity with sequences outside the Plasmodium databases. Four sites of sequence variation were identified in MSP7, all within the MSP7(22) region. The MSP7 gene is expressed in mature schizonts, at the same time as other merozoite surface protein genes. It is proposed that MSP7(22) is the result of cleavage by a protease that may also cleave MSP1 and MSP6. A related gene was identified and cloned from the rodent malaria parasite, Plasmodium yoelii YM; at the amino acid level this sequence was 23% identical and 50% similar to that of P. falciparum MSP7.

摘要

恶性疟原虫的三个品系中已鉴定出编码裂殖子表面蛋白7的基因并进行了测序。该基因编码一个351个氨基酸的多肽,它是裂殖子表面22-kDa蛋白(MSP7(22))的前体,并且在红细胞入侵时与从表面脱落的裂殖子表面蛋白1(MSP1)复合物非共价结合。该复合物的第二个19-kDa组分(MSP7(19))被证明源自MSP7(22),并且该多肽的完整一级结构通过质谱法得到了证实。蛋白质序列包含几个预测的螺旋结构和两个β元件,但与疟原虫数据库之外的序列没有相似性。在MSP7中鉴定出四个序列变异位点,均位于MSP7(22)区域内。MSP7基因在成熟裂殖体中表达,与其他裂殖子表面蛋白基因同时表达。有人提出,MSP7(22)是一种蛋白酶切割的产物,该蛋白酶可能也会切割MSP1和MSP6。从啮齿动物疟原虫约氏疟原虫YM中鉴定并克隆了一个相关基因;在氨基酸水平上,该序列与恶性疟原虫MSP7的序列有23%的同一性和50%的相似性。

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