Matysiak S, Reuthner F, Hoheisel J D
Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Biotechniques. 2001 Oct;31(4):896, 898, 900-2, 904. doi: 10.2144/01314rr01.
A system was establishedfor the parallel synthesis of peptide library arrays in afully automated manner Synthesis takes place in blocks made of polyoxymethylene that hold during all synthesis steps a polypropylene membrane of 8 x 12 cm. Yields are in the nanomole range, obtained at a low consumption of reagents. The current setup is based on a commercially available pipetting robot and supports the generation of 1536 different oligomers/run. Much higher array densities are possible because the membranes are amicable to spot diameters of down to 200 microm, naturally at a cost of the absolute amount produced of each oligomer The method was put to use for the creation of arrayed libraries of peptide nucleic acids (PNAs). These can be employed both as a source of PNA molecules applied individually in experimentation subsequent to their release or as intact oligomer arrays in hybridization analyses.
建立了一个系统,用于以全自动方式平行合成肽库阵列。合成在由聚甲醛制成的模块中进行,这些模块在所有合成步骤中都固定着一张8×12厘米的聚丙烯膜。产率在纳摩尔范围内,试剂消耗低。当前的装置基于市售的移液机器人,每次运行可支持生成1536种不同的寡聚物。由于这些膜适合低至200微米的点样直径,因此可以实现更高的阵列密度,当然,每种寡聚物的绝对产量会有所降低。该方法已用于创建肽核酸(PNA)的阵列文库。这些文库既可以作为释放后单独用于实验的PNA分子来源,也可以作为完整的寡聚物阵列用于杂交分析。