NEW DESORPTION STRATEGIES FOR THE MASS-SPECTROMETRIC ANALYSIS OF MACROMOLECULES

We present two new desorption strategies for the mass spectrometric an alysis of macromolecules. These desorption strategies are based on the molecular design and construction of two general classes of sample 'p robe' surfaces. The first class of surfaces is designed to enhance the desorption of intact macromolecules presented alone (neat) to the sur face; we call this surface-enhanced neat desorption (SEND). The availa bility of probe surfaces derivatized with, or composed of, multiple ty pes and defined numbers of energy-absorbing molecules will facilitate investigations of energy transfer and desorption/ionization mechanisms . The second class of probe surfaces is designed to enhance the desorp tion of specific macromolecules captured directly from unfractionated biological fluids and extracts; we call this surface-enhanced affinity capture (SEAC). Use of these new probe surfaces as chemically defined solid-phase reaction centers will facilitate protein discovery throug h molecular recognition in situ, and also macromolecular structure ana lysis through the sequential chemical and/or enzymatic modification of the adsorbed analyte in situ. Specific examples of laser-assisted SEN D and SEAC time-of-flight mass spectrometry are presented to illustrat e the potential for increased selectivity, analyte detection sensitivi ty, and mass measurement accuracy.