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Investigation of molecular surfaces with time-of-flight secondary ion mass spectrometry

机译:飞行时间二次离子质谱研究分子表面

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TOF-SIMS is a promising technique for evaluating biodevices due to its ultrahigh surface sensitivity. Since a cluster ion source such as C _(60)~+ provides low collision energy per atom, time-of-flight secondary ion mass spectrometry (TOF-SIMS) with the cluster ion is useful for detecting the uppermost surface of molecules immobilized on a substrate, and therefore, enables the evaluation of the orientation of these immobilized biomolecules. Effects of TOF-SIMS with C_(60)~+ were investigated in this study. A relatively small protein, lysozyme, and polypeptides having five amino acid residues, Leu-enkephalin and Met-enkephalin, were employed as model samples. The protein and the polypeptides were immobilized on aminosilanized-indium-tin oxide (ITO) coated glass plates at their N-terminal residues by covalent bonding. The aminosilanized-ITO plate without protein or polypeptide was also prepared as a control sample. After freeze-drying, the samples were measured with TOF-SIMS using gallium and C _(60)~+ cluster ion sources, and then TOF-SIMS spectra were analyzed to select peaks specific to each biomolecule by a comparison between the samples. As a result, the C_(60)~+ primary ion source showed advantages in evaluating biomolecules, because more peaks at a higher mass generated from the biomolecules can be obtained using C_(60)~+ than Ga~+ or Au_3~+ as the primary ion source, although no difference was detected between the two polypeptide samples under the current measurement conditions.
机译:TOF-SIMS具有超高的表面灵敏度,是一种用于评估生物设备的有前途的技术。由于诸如C _(60)〜+之类的簇离子源每个原子提供的碰撞能量较低,因此带有簇离子的飞行时间二次离子质谱(TOF-SIMS)可用于检测固定在其上的分子的最表面因此,能够评估这些固定化生物分子的取向。研究了TOF-SIMS对C_(60)〜+的影响。使用相对较小的蛋白质,溶菌酶和具有五个氨基酸残基的多肽亮氨酸脑啡肽和蛋氨酸脑啡肽作为模型样品。通过共价键合,将蛋白质和多肽的N末端残基固定在氨基硅烷化铟锡氧化物(ITO)涂层的玻璃板上。还制备了没有蛋白质或多肽的氨基硅烷化的ITO板作为对照样品。冷冻干燥后,使用镓和C _(60)〜+簇离子源用TOF-SIMS测量样品,然后通过样品之间的比较分析TOF-SIMS光谱以选择特定于每种生物分子的峰。结果,C_(60)〜+初级离子源在评估生物分子方面显示出优势,因为使用C_(60)〜+可以比Ga〜+或Au_3〜+获得更多从生物分子产生的更高质量的峰。尽管在当前测量条件下两个多肽样品之间未检测到差异,但仍是主要离子源。

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