Huanwen Chen
Jiangxi Key Laboratory for Mass Spectrometry and Instrumentation, China
Title: Extractive Electrospray Ionization Mass Spectrometry For Biosample Analysis
Biography
Biography: Huanwen Chen
Abstract
Mass spectrometry (MS) is one of the preferable analytical techniques for sensitive characterization of biological samples on the molecular levels. Technological innovations advance mass spectrometry for sophisticate applications in many fields including but not limited to chemistry, material sciences and life sciences. For trace analysis of a typical biological sample, classical MS techniques require multi-step sample pre-treatment (e.g., grinding, extraction, separation, pre-concentration, etc.) to obtain molecular information from the native biological samples, especially for detection of trace analytes distributed in the 3-dimensional volume of a bulk sample[1,2]. Commonly associated with sample pre-treatment are biological degradation, chemical reactions, reagent contamination, and material losses. Apparently, tedious sample pretreatments strangle the breakthrough of high throughput in analytical mass spectrometry.
By isolating the high electric filed required for ionization from any biological sample, extractive electrospray ionization (EESI) allows direct detection of small metabolites and/or large proteins distributed either on surfaces or inside bulk tissue by mass spectrometry, without any sample pretreatment. Experiments demonstrated that EESI-MS minimizes matrix effects during the ionization process, enabling real-time, in vivo analysis of biofluids, biosurfaces, aerosols and living objectives. Therein the fundamental principle, instrumentation and typical applications of EESI-MS for biological analysis would be summarized, giving emphases on progresses in our lab for sensitive qualitative/quantitative detection of chemicals located inside a bulk tissue of whole-volume (≥20 mm3), with neither mashing/grinding the sample nor matrixes clean-up[3-5]. Furthermore, the emerging utilization of EESI-MS for sequentially acquiring metabolites, lipids, and proteins in a single tissue sample will be presented for the first time.