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A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission.一种疟蚊唾液腺蛋白部分抑制疟原虫孢子穿透和传播。
Nat Commun. 2018 Jul 25;9(1):2908. doi: 10.1038/s41467-018-05374-3.
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Immunization with AgTRIO, a Protein in Anopheles Saliva, Contributes to Protection against Plasmodium Infection in Mice.经 AgTRIO(一种按蚊唾液蛋白)免疫可促进小鼠抵抗疟原虫感染。
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Longitudinal analysis of Plasmodium sporozoite motility in the dermis reveals component of blood vessel recognition.疟原虫子孢子在真皮层活动的纵向分析揭示了血管识别的组成部分。
Elife. 2015 Aug 13;4:e07789. doi: 10.7554/eLife.07789.
2
Quantum dot-based multiphoton fluorescent pipettes for targeted neuronal electrophysiology.基于量子点的多光子荧光管用于靶向神经元电生理学。
Nat Methods. 2014 Dec;11(12):1237-1241. doi: 10.1038/nmeth.3146. Epub 2014 Oct 19.
3
Study of normal and pathological blood vessel morphogenesis in Flt1-tdsRed BAC Tg mice.Flt1-tdsRed BAC转基因小鼠正常和病理性血管形态发生的研究。
Genesis. 2012 Jul;50(7):561-71. doi: 10.1002/dvg.22031. Epub 2012 May 26.
4
Host cell traversal is important for progression of the malaria parasite through the dermis to the liver.宿主细胞穿越对于疟原虫通过真皮进入肝脏的进程很重要。
Cell Host Microbe. 2008 Feb 14;3(2):88-96. doi: 10.1016/j.chom.2007.12.007.
5
Dry beveling micropipettes using a computer hard drive.使用电脑硬盘对微量移液器进行干式斜切。
J Neurosci Methods. 2006 Nov 15;158(1):19-21. doi: 10.1016/j.jneumeth.2006.05.009. Epub 2006 Jun 16.
6
Quantitative imaging of Plasmodium transmission from mosquito to mammal.疟原虫从蚊子到哺乳动物传播的定量成像。
Nat Med. 2006 Feb;12(2):220-4. doi: 10.1038/nm1350. Epub 2006 Jan 22.
7
Bright fluorescent nanodiamonds: no photobleaching and low cytotoxicity.明亮的荧光纳米金刚石:无光漂白且细胞毒性低。
J Am Chem Soc. 2005 Dec 21;127(50):17604-5. doi: 10.1021/ja0567081.

用于荧光显微镜的微管的稳健荧光标记:在观察蚊子传播的寄生虫感染中的应用。

Robust fluorescent labelling of micropipettes for use in fluorescence microscopy: application to the observation of a mosquito borne parasite infection.

机构信息

Johns Hopkins Malaria Research Institute and Department of Molecular Microbiology & Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, U.S.A.

Laboratory of Molecular Biophysics, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, U.S.A.

出版信息

J Microsc. 2018 Jan;269(1):78-84. doi: 10.1111/jmi.12610. Epub 2017 Aug 10.

DOI:10.1111/jmi.12610
PMID:28795398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6590669/
Abstract

The ability to monitor micropipette injections with a high-resolution fluorescent microscope has utility for a variety of applications. Herein, different approaches were tested for creating broad-band fluorescently labelled glass micropipettes including: UV cured glass glues, baked glass enamel containing fluorescent dyes as well as nanodiamonds attached during pipette formation in the microforge. The most robust and simplest approach was to use labelled baked enamel on the exterior of the pipette. This approach was tested using pipettes designed to mimic a mosquito proboscis for the injection of the malaria parasite, Plasmodium spp., into the dermis of a living mouse ear. The pipette (∼30 micron diameter) was easily detected in the microscopy field of view and tolerated multiple insertions through the skin. This simple inexpensive approach to fluorescently labelling micropipettes will aid in the development of procedures under the fluorescent microscope.

摘要

使用高分辨率荧光显微镜监测微量移液器注射具有多种应用的实用性。本文测试了几种不同的方法来创建宽带荧光标记的玻璃微量移液器,包括:紫外线固化玻璃胶、含有荧光染料的烤玻璃瓷漆以及在微 forge 中形成微量移液器时附着的纳米金刚石。最稳健、最简单的方法是在微量移液器的外部使用标记的烤瓷漆。该方法使用设计用于模拟蚊子喙的微量移液器进行了测试,用于将疟疾寄生虫 Plasmodium spp.注入活鼠耳的真皮中。该微量移液器(直径约 30 微米)在显微镜视野中很容易被检测到,并且可以耐受多次通过皮肤的插入。这种简单且廉价的荧光标记微量移液器的方法将有助于在荧光显微镜下开发程序。