By Mahmoud H. Hamdan, Pier G. Righetti

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Additional info for Proteomics Today: Protein Assessment and Biomarkers Using Mass Spectrometry, 2D Electrophoresis,and Microarray Technology

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Cryogenic detectors have been developed since the early 1980s for applications in particle physics, astrophysics, and material analysis. There are a number of reasons behind their use in these diverse fields. These include high resolving power, low energy threshold, and large, sensitive absorbing areas. The ability of these detectors to detect slow-moving massive ions with near 100% efficiency and the additional information gained from measuring the energy of the same ions have attracted a number of attempts to use them in TOF–MS.

In fact, single-amino-acid replacement accounts for almost 95% of all known hemoglobin variants. Although the substitution of one amino acid out of 141 (␣-chain) or 146 (␤-chain) may sound like a small difference, it can have substantial influence on the function and stability of the entire molecule. For example, sickle cell anemia (Ingram, 1959) is caused by a ␤-chain variant which has a Glu replaced by Val in position 6. Other mutations can have more dramatic effects on the sequence of the chain.

Microchannel Plates (MCPs) Essentially, an MCP is an array of 104 –107 capillary-type electron multipliers oriented parallel to each other and having channel diameters in the range of 10–100 ␮m. 4b gives a schematic diagram of a single channel. The main characteristics of MCP devices have been reviewed by Wiza (1979) together with a description of various configurations that have been fabricated for use as ion detectors in MS. 4. (a) Cutaway view of microchannel plate and (b) schematic view of single channel of microchannel plate (based on schemes published in various catalogs by Galileo Electro-Optics).

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