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Fluorescence-activated cell-sorting analysis of fibronectin peptides binding to Trypanosoma cruzi trypomastigotes.

作者信息

Quaissi M A, Kusnierz J P, Gras-Masse H, Drobecq H, Velge P, Cornette J, Capron A, Tartar A

机构信息

Centre d'Immunologie et de Biologie Parasitaire, Unité Mixte INSERM 167--CNRS 624, Lille, France.

出版信息

J Protozool. 1988 Feb;35(1):111-4. doi: 10.1111/j.1550-7408.1988.tb04087.x.

DOI:10.1111/j.1550-7408.1988.tb04087.x
PMID:3284996
Abstract

The binding of synthetic peptides modeled from the sequence of the cell attachment site of fibronectin to T. cruzi trypomastigote surface receptors was investigated by fluorescence-activated cell-sorting analysis using fluorescein-labeled peptides. Peptides with the sequence Arg-Gly-Asp-Ser bound to the parasite surface. A low percentage of fresh parasites recently liberated from infected fibroblasts had the capacity to bind the peptide. In contrast, these parasites showed a time-dependent several-fold increase in their ability to bind the Arg-Gly-Asp-Ser-containing peptides during extracellular incubation. From these observations, it appears that the expression of surface receptors on a particular, mature stage of the parasite parallels its ability to adhere to and infect host cells.

摘要

相似文献

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Trypanosoma cruzi infection inhibited by peptides modeled from a fibronectin cell attachment domain.
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