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恶性疟原虫在体外培养过程中释放的多肽

Plasmodium falciparum polypeptides released during in vitro cultivation.

作者信息

Rodriguez da Silva L, Loche M, Dayal R, Perrin L H

出版信息

Bull World Health Organ. 1983;61(1):105-12.

Abstract

Synchronous cultures of Plasmodium falciparum were successively labelled with ((35)S)-methionine and both the supernatants and the pellets of infected red blood cells were collected. The release of TCA-precipitable material in the culture supernatants was low during the development of ring forms and trophozoites, increased during schizogony, and was maximum at the time of schizont rupture and merozoite reinvasion. Analysis of the supernatants by SDS - PAGE and autoradiography showed that both polypeptides common to the various developmental stages of the parasite and schizont/merozoite-specific polypeptides were released. Polypeptides of relative molecular mass 140 000, 82 000 and, to a lower degree, 41 000 were present in high amounts in the culture supernatants. These polypeptides have been shown to be the target of monoclonal antibodies that are able to inhibit the growth of P. falciparum cultures, and may be involved in protective immunity. The released polypeptides may also be used as target antigens in immunodiagnostic tests aiming at the detection of malaria infection.

摘要

恶性疟原虫同步培养物先后用(³⁵S)-甲硫氨酸标记,收集感染红细胞的上清液和沉淀。在环状体和滋养体发育期间,培养上清液中三氯乙酸可沉淀物质的释放量较低,在裂殖生殖期间增加,在裂殖体破裂和裂殖子再侵入时达到最大值。通过SDS-PAGE和放射自显影分析上清液表明,寄生虫各个发育阶段共有的多肽以及裂殖体/裂殖子特异性多肽都被释放出来。相对分子质量为140000、82000以及程度较低的41000的多肽大量存在于培养上清液中。这些多肽已被证明是能够抑制恶性疟原虫培养物生长的单克隆抗体的靶点,并且可能参与保护性免疫。释放的多肽也可用作免疫诊断试验中的靶抗原,用于检测疟疾感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d44/2536053/1ff620296852/bullwho00097-0117-a.jpg

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