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深入了解杜氏利什曼原虫前鞭毛体生长和分化过程中的组成性蛋白质组。

An Insight into the Constitutive Proteome Throughout Leishmania donovani Promastigote Growth and Differentiation.

机构信息

Laboratory of Molecular Parasitology, Department of Cellular and Molecular Biology, Centro de Investigaciones Biológicas (Consejo Superior de Investigaciones Científicas), Calle Ramiro de Maeztu 9, 28040, Madrid, Spain.

Service of Proteomics and Genomics, Centro de Investigaciones Biológicas (Consejo Superior de Investigaciones Científicas), Calle Ramiro de Maeztu 9, 28040, Madrid, Spain.

出版信息

Int Microbiol. 2019 Mar;22(1):143-154. doi: 10.1007/s10123-018-00036-2. Epub 2018 Nov 16.

Abstract

Anthroponotic visceral leishmaniasis is a life-threatening disease caused by Leishmania donovani (Kinetoplastida: Trypanosomatidae) in East Africa and the Indian subcontinent. Unlike promastigote growth and differentiation in the sand fly gut or in axenic culture, L. donovani promastigote-into-amastigote development has been studied by high-throughput gene expression profiling. In this study, we have identified abundant constitutive proteins in axenically cultured promastigotes by two-dimension electrophoresis and matrix-assisted laser desorption-ionization tandem time-of-flight (MALDI-TOF/TOF) mass spectrometry. Most proteins involved in the trypanothione-based redox antioxidant system are expressed constitutively throughout axenic L. donovani promastigote growth and differentiation (tryparedoxin, trypanothione peroxidase, generic peroxidoxin, iron-superoxide dismutase, and elongation factor 1β). These findings are in agreement with previous data on other Old World species (i.e., L. major and L. infantum), whereas New World species (i.e., L. amazonensis and L. pifanoi) and Crithidia fasciculata show different expression patterns.

摘要

人源内脏利什曼病是一种由利什曼原虫(Kinetoplastida:锥虫科)在东非和印度次大陆引起的危及生命的疾病。与在沙蝇肠道或在无细胞培养中增长和分化的前鞭毛体不同,利什曼原虫前鞭毛体向无鞭毛体的发育已经通过高通量基因表达谱进行了研究。在这项研究中,我们通过二维电泳和基质辅助激光解吸离子化串联飞行时间(MALDI-TOF/TOF)质谱法鉴定了无细胞培养的前鞭毛体中丰富的组成型蛋白。参与基于三肽硫醇的氧化还原抗氧化系统的大多数蛋白在前鞭毛体的整个无细胞生长和分化过程中都有表达(硫氧还蛋白、硫氧还蛋白过氧化物酶、普通过氧化物酶、铁超氧化物歧化酶和延伸因子 1β)。这些发现与以前对其他旧世界物种(即利什曼原虫和婴儿利什曼原虫)的数据一致,而新世界物种(即利什曼原虫和利什曼原虫)和 Crithidia fasciculata 表现出不同的表达模式。

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