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Evaluation of micro-electrospray ionization with ion mobility spectrometry/mass spectrometry
Institution:1. Washington State University, Chemistry Department, Pullman, Washington, 99164-4630, USA;1. Dept. Mecánica de Fluidos y Propulsión Aeroespacial, ETS Ingeniería Aeronáutica y del Espacio, Universidad Politécnica de Madrid, Plza. Cardenal Cisneros 3, Madrid 28040, Spain;2. Dept. Arquitectura, Construcción y Sistemas Oceánicos y Navales, ETSI Navales, Universidad Politécnica de Madrid, Avda. de la Memoria 4, Madrid 28040, Spain;3. Dept. Química Física I, Facultad de C.C. Químicas, Universidad Complutense de Madrid, Plza. de Ciencias 2, Madrid 28040, Spain;1. Univ. Lille, INSERM, U1192 - Laboratoire Protéomique, Réponse Inflammatoire et Spectrométrie de Masse-PRISM, F-59000 Lille, France;2. Univ. Lille, CNRS, UMR 8523 - PhLAM - Physique des Lasers Atomes et Molécules, F-59000 Lille, France;3. Sorbonne Universités, UPMC Univ Paris 06, Ecole Normale Supérieure, CNRS, Laboratoire des Biomolecules (LBM), 4 place Jussieu, 75005 Paris, France;1. Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 People''s Republic of China;2. University of Chinese Academy of Sciences, 19 Yuquan Road, Beijing 100039 People''s Republic of China
Abstract:In recent years, the resolving power of ion mobility instruments has been increased significantly, enabling ion mobility spectrometry (IMS) to be utilized as an analytical separation technique for complex mixtures. In theory, decreasing the drift tube temperature results in increased resolution due to decreased ion diffusion. However, the heat requirements for complete ion desolvation with electrospray ionization (ESI) have limited the reduction of temperatures in atmospheric pressure ion mobility instruments. Micro-electrospray conditions were investigated in this study to enable more efficient droplet formation and ionization with the objective of reducing drift tube temperatures and increasing IMS resolution. For small molecules (peptides), the drift tube temperature was reduced to ambient temperature with good resolution by employing reduced capillary diameters and flow rates. By employing micro-spray conditions, experimental resolution values approaching theoretically predicted resolution were achieved over a wide temperature range (30 to 250 °C). The historical heat requirements of atmospheric pressure IMS due to ESI desolvation were eliminated due to the use of micro-spray conditions and the high-resolution IMS spectra of GLY-HIS-LYS was obtained at ambient temperature. The desolvation of proteins (cytochrome c) was found to achieve optimal resolution at temperatures greater than 125 °C. This is significantly improved from earlier IMS studies that required drift tube temperatures of 250°C for protein desolvation.
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