Piret Gaëlle, Drobecq Hervé, Boukherroub Rabah, Melnyk Oleg
Institut de Recherche Interdisciplinaire, CNRS-USR 3078, Villeneuve d'Ascq, France.
Methods Mol Biol. 2010;669:125-33. doi: 10.1007/978-1-60761-845-4_10.
Peptide microarrays are useful devices for the high throughput study of biomolecular or peptide-cell interactions. Whereas the synthesis of unmodified peptide libraries is an easy task and can be performed at reasonable cost, the synthesis of libraries of modified peptides remains expensive and time consuming. This bottleneck led us to examine the possibility to produce modified peptide microspots by in situ chemical modification of unmodified peptide microspots. The great advantage would be the preparation of a series of complex microarrays (daughter microarrays) starting from an easy-to-make and cost-effective unmodified peptide microarray (parent microarray). One step toward this goal has been presented in the accompanying chapter dealing with the in situ methylation methodology for studying the specificity of antibodies directed toward methylated epitopes. Here we describe the development of a novel desorption/ionization on silicon nanowires mass spectrometry (DIOSiNWs-MS) technique for characterizing the in situ chemical modification of peptides.
肽微阵列是用于生物分子或肽 - 细胞相互作用高通量研究的有用工具。虽然未修饰肽库的合成是一项容易的任务,并且可以以合理的成本进行,但修饰肽库的合成仍然昂贵且耗时。这一瓶颈促使我们研究通过对未修饰肽微点进行原位化学修饰来制备修饰肽微点的可能性。其巨大优势在于从易于制备且成本效益高的未修饰肽微阵列(母微阵列)出发,制备一系列复杂的微阵列(子微阵列)。朝着这一目标迈出的一步已在随附章节中有所介绍,该章节涉及用于研究针对甲基化表位的抗体特异性的原位甲基化方法。在此,我们描述了一种用于表征肽原位化学修饰的新型硅纳米线解吸/电离质谱(DIOSiNWs-MS)技术的开发。