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Tape-Arabidopsis Sandwich - a Simpler Arabidopsis Protoplast Isolation Method

机译:带状拟南芥三明治-一种更简单的拟南芥原生质体分离方法

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BackgroundProtoplasts isolated from leaves are useful materials in plant research. One application, the transient expression of recombinant genes using Arabidopsis mesophyll protoplasts (TEAMP), is currently commonly used for studies of subcellular protein localization, promoter activity, and in vivo protein-protein interactions. This method requires cutting leaves into very thin slivers to collect mesophyll cell protoplasts, a procedure that often causes cell damage, may yield only a few good protoplasts, and is time consuming. In addition, this protoplast isolation method normally requires a large number of leaves derived from plants grown specifically under low-light conditions, which may be a concern when material availability is limited such as with mutant plants, or in large scale experiments. ResultsIn this report, we present a new procedure that we call the Tape-Arabidopsis Sandwich. This is a simple and fast mesophyll protoplast isolation method. Two kinds of tape (Time tape adhered to the upper epidermis and 3 M Magic tape to the lower epidermis) are used to make a \u22Tape-Arabidopsis Sandwich\u22. The Time tape supports the top side of the leaf during manipulation, while tearing off the 3 M Magic tape allows easy removal of the lower epidermal layer and exposes mesophyll cells to cell wall digesting enzymes when the leaf is later incubated in an enzyme solution. The protoplasts released into solution are collected and washed for further use. For TEAMP, plasmids carrying a gene expression cassette for a fluorescent protein can be successfully delivered into protoplasts isolated from mature leaves grown under optimal conditions. Alternatively, these protoplasts may be used for bimolecular fluorescence complementation (BiFC) to investigate protein-protein interactions in vivo, or for Western blot analysis. A significant advantage of this protocol over the current method is that it allows the generation of protoplasts in less than 1 hr, and allows TEAMP transfection to be carried out within 2 hr. ConclusionThe protoplasts generated by this new Tape-Arabidopsis Sandwich method are suitable for the same range of research applications as those that use the current method, but require less operator skill, equipment and time.
机译:背景从叶中分离出的原生质体是植物研究中的有用材料。一种应用是使用拟南芥叶肉原生质体(TEAMP)瞬时表达重组基因,目前通常用于研究亚细胞蛋白定位,启动子活性和体内蛋白-蛋白相互作用。该方法需要将叶子切成很细的条状以收集叶肉细胞原生质体,该过程通常会导致细胞损伤,可能只产生少量良好的原生质体,而且很费时间。此外,这种原生质体分离方法通常需要大量叶片,这些叶片得自专门在弱光条件下生长的植物,当有限的材料(如突变植物)或大规模实验时,这可能是一个问题。结果在本报告中,我们提出了一种称为“拟南芥胶带”的新方法。这是一种简单快速的叶肉原生质体分离方法。两种胶带(Time胶带粘在上表皮上,3 M Magic胶带粘在下表皮上)用于制作tape-Arabidopsis Sandwich。在操作过程中,Time胶带支撑叶子的顶部,而撕下3 M Magic胶带则可以轻松去除下表皮层,并在稍后将叶子在酶溶液中孵育时将叶肉细胞暴露于细胞壁消化酶中。收集释放到溶液中的原生质体并洗涤以备进一步使用。对于TEAMP,可以将带有荧光蛋白基因表达盒的质粒成功地传递到原生质体中,该原生质体是从在最佳条件下生长的成熟叶片中分离出来的。或者,这些原生质体可用于双分子荧光互补(BiFC),以研究体内蛋白质之间的相互作用,或用于蛋白质印迹分析。该协议相对于当前方法的显着优势在于,它允许在不到1小时的时间内生成原生质体,并允许TEAMP转染在2小时内进行。结论通过这种新的Tape-Arabidopsis Sandwich方法产生的原生质体适用于与使用当前方法的研究范围相同的研究应用,但所需的操作技能,设备和时间更少。

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