Nayak Ranu, Knapp Daniel R
Department of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, 173 Ashley Avenue, Charleston, South Carolina 29425, USA.
Anal Chem. 2007 Jul 1;79(13):4950-6. doi: 10.1021/ac062289u. Epub 2007 Jun 5.
Nanoporous aluminum oxide layers, grown by anodization of aluminum thin films on glass and then sputter-coated with gold, were used to study the effects of the thin-film structural parameters on laser desorption/ionization (LDI) mass spectrometry (MS) of peptides. Variation of MS signal intensity was examined as a function of alumina pore depth, pore width, and gold layer thickness. Peptide molecular ion intensity was optimal with porous alumina formed from aluminum films of approximately 600-nm thickness; thinner or thicker films gave significantly lower signals. Signals decreased when pore sizes were increased beyond the as-formed width of approximately 100 nm. The MS signal also varied with the thickness of the sputtered gold layer with an optimum thickness being approximately 90 nm. The results of these studies provide values for empirical optimization of LDI MS performance as well as potential clues to the LDI mechanism.
通过对玻璃上的铝薄膜进行阳极氧化,然后溅射金涂层生长的纳米多孔氧化铝层,用于研究薄膜结构参数对肽的激光解吸/电离(LDI)质谱(MS)的影响。研究了质谱信号强度随氧化铝孔径深度、孔径宽度和金层厚度的变化。当由厚度约为600nm的铝膜形成多孔氧化铝时,肽分子离子强度最佳;更薄或更厚的膜给出的信号明显更低。当孔径增加到超过约100nm的初始形成宽度时,信号降低。质谱信号也随溅射金层的厚度而变化,最佳厚度约为90nm。这些研究结果为LDI质谱性能的经验优化提供了数值,也为LDI机制提供了潜在线索。