Shi Fengjian, Flanigan Paul M, Archer Jieutonne J, Levis Robert J
†Department of Chemistry, Temple University, 1901 North 13th Street, Philadelphia, Pennsylvania 19122, United States.
‡Center for Advanced Photonics Research, Temple University, 1901 North 13th Street, Philadelphia, Pennsylvania 19122, United States.
Anal Chem. 2015 Mar 17;87(6):3187-94. doi: 10.1021/ac502563c. Epub 2015 Feb 26.
A fiber-based laser with a pulse duration of 435 fs and a wavelength of 1042 nm was used to vaporize biological macromolecules intact from the condensed phase into the gas phase for nanospray postionization and mass analysis. Laser vaporization of dried standard protein samples from a glass substrate by 10 Hz bursts of 20 pulses having 10 μs pulse separation and <50 μJ pulse energy resulted in signal comparable to a metal substrate. The protein signal observed from an aqueous droplet on a glass substrate was negligible compared to either a droplet on metal or a thin film on glass. The mass spectra generated from dried and aqueous protein samples by the low-energy, fiber laser were similar to the results from high-energy (500 μJ), 45-fs, 800-nm Ti:sapphire-based femtosecond laser electrospray mass spectrometry (LEMS) experiments, suggesting that the fiber-based femtosecond laser desorption mechanism involves a nonresonant, multiphoton process, rather than thermal- or photoacoustic-induced desorption. Direct analysis of whole blood performed without any pretreatment resulted in features corresponding to hemoglobin subunit-heme complex ions. The observation of intact molecular ions with low charge states from protein, and the tentatively assigned hemoglobin α subunit-heme complex from blood suggests that fiber-based femtosecond laser vaporization is a "soft" desorption source at a laser intensity of 2.39 × 10(12) W/cm(2). The low-energy, turnkey fiber laser demonstrates the potential of a more robust and affordable laser for femtosecond laser vaporization to deliver biological macromolecules into the gas phase for mass analysis.
使用脉冲持续时间为435飞秒、波长为1042纳米的光纤激光器,将生物大分子从凝聚相完整地汽化为气相,用于纳米喷雾后电离和质谱分析。通过10赫兹的20个脉冲(脉冲间隔为10微秒,脉冲能量<50微焦)对玻璃基板上的干燥标准蛋白质样品进行激光汽化,得到的信号与金属基板相当。与金属上的液滴或玻璃上的薄膜相比,在玻璃基板上的水滴中观察到的蛋白质信号可忽略不计。由低能量光纤激光器对干燥和含水蛋白质样品产生的质谱与高能(500微焦)、45飞秒、800纳米钛宝石基飞秒激光电喷雾质谱(LEMS)实验的结果相似,这表明基于光纤的飞秒激光解吸机制涉及非共振多光子过程,而不是热诱导或光声诱导解吸。未经任何预处理对全血进行直接分析,得到了与血红蛋白亚基-血红素复合离子相对应的特征峰。从蛋白质中观察到低电荷态的完整分子离子,以及从血液中初步确定的血红蛋白α亚基-血红素复合物,表明在激光强度为2.39×10(12)瓦/平方厘米时,基于光纤的飞秒激光汽化是一种“软”解吸源。这种低能量、交钥匙式光纤激光器展示了一种更强大且价格更实惠的激光器在飞秒激光汽化方面的潜力,可将生物大分子输送到气相中进行质谱分析。