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在体外抑制恶性疟原虫入侵的单克隆抗体可识别裂殖子表面蛋白-1的首个生长因子样结构域。

Monoclonal antibodies that inhibit Plasmodium falciparum invasion in vitro recognise the first growth factor-like domain of merozoite surface protein-1.

作者信息

Chappel J A, Holder A A

机构信息

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

出版信息

Mol Biochem Parasitol. 1993 Aug;60(2):303-11. doi: 10.1016/0166-6851(93)90141-j.

Abstract

A major protein found on the surface of the invasive stage of the malaria parasite Plasmodium falciparum, merozoite surface protein-1 (MSP1), has been proposed as a vaccine candidate. Antibodies which recognise a single fragment of this molecule (MSP1(19)), composed of 2 regions related to epidermal growth factor (EGF), also inhibit parasite growth in vitro. It is shown by direct expression of the individual EGF-like domains in Escherichia coli, that the first domain is the target of growth-inhibitory antibodies. A single amino acid difference influences the binding of some antibodies to this domain.

摘要

恶性疟原虫侵袭期表面发现的一种主要蛋白质——裂殖子表面蛋白1(MSP1),已被提议作为候选疫苗。识别该分子单个片段(MSP1(19))的抗体,由与表皮生长因子(EGF)相关的2个区域组成,在体外也能抑制寄生虫生长。通过在大肠杆菌中直接表达各个EGF样结构域表明,第一个结构域是生长抑制性抗体的靶点。单个氨基酸差异会影响某些抗体与该结构域的结合。

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