Agricultural Biotechnology Research Center, Academia Sinica, Taipei, 115, Taiwan.
Plant Methods. 2009 Nov 24;5:16. doi: 10.1186/1746-4811-5-16.
Protoplasts 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.
In 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 "Tape-Arabidopsis Sandwich". 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.
The 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.
从叶片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,该方法目前常用于亚细胞蛋白定位、启动子活性以及体内蛋白-蛋白相互作用的研究。这种方法需要将叶片切成非常薄的薄片以收集叶肉细胞原生质体,该过程通常会导致细胞损伤,可能只能得到少数几个好的原生质体,并且耗时。此外,这种原生质体分离方法通常需要大量的叶片,这些叶片来自于在低光条件下生长的植物,当材料可用性有限时,例如对于突变体植物或大规模实验,这可能是一个问题。
在本报告中,我们提出了一种新的程序,称为胶带-拟南芥三明治法。这是一种简单快速的叶肉原生质体分离方法。两种胶带(Time 胶带粘附在上表皮,3M 魔术胶带粘附在下表皮)用于制作“胶带-拟南芥三明治”。Time 胶带在操作过程中支撑叶片的上表面,而撕下 3M 魔术胶带可轻松去除下表皮层,并在稍后将叶片孵育在酶溶液中时,使叶肉细胞暴露于细胞壁消化酶中。释放到溶液中的原生质体被收集并洗涤以供进一步使用。对于 TEAMP,可以成功地将携带荧光蛋白表达盒的质粒递送到在最佳条件下生长的成熟叶片中分离出的原生质体中。或者,可以将这些原生质体用于双分子荧光互补(BiFC)以研究体内蛋白质-蛋白质相互作用,或用于 Western blot 分析。与当前方法相比,该方案的一个显著优势是,它可以在不到 1 小时内产生原生质体,并可以在 2 小时内完成 TEAMP 转染。
使用新的胶带-拟南芥三明治法产生的原生质体适用于与当前方法相同范围的研究应用,但需要较少的操作技能、设备和时间。