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Biomolecules ionization

Modern commercial lasers can produce intense beams of monochromatic, coherent radiation. The whole of the UV/visible/IR spectral range is accessible by suitable choice of laser. In mass spectrometry, this light can be used to cause ablation, direct ionization, and indirect ionization (MALDI). Ablation (often together with a secondary ionization mode) and MALDI are particularly important for examining complex, intractable solids and large polar biomolecules, respectively. [Pg.136]

The ablated vapors constitute an aerosol that can be examined using a secondary ionization source. Thus, passing the aerosol into a plasma torch provides an excellent means of ionization, and by such methods isotope patterns or ratios are readily measurable from otherwise intractable materials such as bone or ceramics. If the sample examined is dissolved as a solid solution in a matrix, the rapid expansion of the matrix, often an organic acid, covolatilizes the entrained sample. Proton transfer from the matrix occurs to give protonated molecular ions of the sample. Normally thermally unstable, polar biomolecules such as proteins give good yields of protonated ions. This is the basis of matrix-assisted laser desorption ionization (MALDI). [Pg.399]

APPLICATION OF SURFACE-ASSISTED LASER DESORPTION IONIZATION TO THE DETECTION OF BIOMOLECULES... [Pg.140]

Matrix-assisted laser desorption mass spectrometry (MALDI-MS) is, after electrospray ionization (ESI), the second most commonly used method for ionization of biomolecules in mass spectrometry. Samples are mixed with a UV-absorbing matrix substance and are air-dried on a metal target. Ionization and desorption of intact molecular ions are performed using a UV laser pulse. [Pg.748]

The mass spectrum produced should provide unambiguous molecular weight information from the wide range of compounds amenable to analysis by HPLC, including biomolecules with molecular weights in excess of 1000 Da. The study of these types of molecule by mass spectrometry may be subject to limitations associated with their ionization and detection and the mass range of the instrument being used. [Pg.22]

The APCl ionization regime is much more harsh that ESI and this precludes its use for the study of large biomolecules, with the mass limit for APCl being generally considered as below 2000 Da. Having said this, as will be shown later, the technique may still be used for the analysis of many thermally labile compounds without their decomposition, and small peptides have been studied. [Pg.183]

ESI-MS has emerged as a powerful technique for the characterization of biomolecules, and is the most versatile ionization technique in existence today. This highly sensitive and soft ionization technique allows mass spectrometric analysis of thermolabile, non-volatile, and polar compounds and produces intact ions from large and complex species in solution. In addition, it has the ability to introduce liquid samples to a mass detector with minimum manipulation. Volatile acids (such as formic acid and acetic acid) are often added to the mobile phase as well to protonate anthocyanins. A chromatogram with only the base peak for every mass spectrum provides more readily interpretable data because of fewer interference peaks. Cleaner mass spectra are achieved if anthocyanins are isolated from other phenolics by the use of C18 solid phase purification. - ... [Pg.493]

Metastable atom bombardment (MAB) is a novel ionization method for mass spectrometry invented by Michel Bertrand s group at the University of Montreal, Quebec, Canada, and described by Faubert et al.38 For the identification of bacteria by MS, MAB has a number of significant advantages relative to more familiar ionization techniques. Electron ionization (El) imparts so much excess energy that labile biomolecules break into very small fragments, from which the diagnostic information content is limited since all... [Pg.104]

Flowever, the object being analyzed has to be removed from the tissues. Thus, information about the distribution of the target in the organism or in the cells is inevitably lost. What is now needed is a technology to acquire information about the distribution of the biomolecule simultaneously with its identification. The method used for this purpose, called imaging mass spectrometry (IMS), is as follows. The tissue sample is cut into thin slices, and a matrix that assists the ionization of macromolecules is spread onto these slices. The macromolecules are then ionized by a scanning laser, and the generated ions are detected and analyzed by MS.1... [Pg.369]

Matrix Assisted Laser Desorption Ionization. During the development of MS, a lot of studies have been devoted to the use of laser light as an energy source for ionizing molecules. As a result, in the mid 1980s MALDI[5] was introduced and soon applied to the study of large molecules.[18] Koichi Tanaka was jointly awarded the Nobel Prize for Chemistry in 2002 for the study of large biomolecules by MALDI. [Pg.51]

The MALDI-TOF technique was first developed for the analysis of large biomolecules (Karas and others 1987). This technique presents some interesting characteristics. Of these, the high speed of analysis and the sensitivity of the technique have been pointed out as important advantages compared with other methods. In MALDI the samples are cocrystallized with a matrix that is usually composed of organic compounds, such as 3,5-dimethoxy-4-hydroxycinnamic acid (sinapic acid), 2, 4, 6 -trihydroxyacetophenone, a-cyano-4-hydroxycinnamic acid (alpha-cyano or alpha-matrix), and 2,5-dihydroxybenzoic acid (DHB). After the cocrystallization, the laser is fired and the matrix absorbs energy and allows a soft ionization of the samples. Afterward the ions are analyzed by a TOF mass spectrometer. [Pg.63]

B. Spengler. Post-Source Decay Analysis in Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry of Biomolecules. J. Mass Spectrom., 32(1997) 1019-1036. [Pg.102]

Why are desorption ionization techniques well suited to the analysis of biomolecules (they do not depend on thermal energy to volatilize analytes). [Pg.400]

Proteins and other large biomolecules can be analyzed using MALDI (matrix-assisted laser desorption and ionization) with TOF... [Pg.780]


See other pages where Biomolecules ionization is mentioned: [Pg.204]    [Pg.75]    [Pg.204]    [Pg.75]    [Pg.136]    [Pg.291]    [Pg.545]    [Pg.140]    [Pg.137]    [Pg.72]    [Pg.56]    [Pg.98]    [Pg.289]    [Pg.269]    [Pg.57]    [Pg.481]    [Pg.13]    [Pg.12]    [Pg.40]    [Pg.47]    [Pg.105]    [Pg.250]    [Pg.239]    [Pg.300]    [Pg.315]    [Pg.15]    [Pg.366]    [Pg.66]    [Pg.74]    [Pg.333]    [Pg.75]    [Pg.243]    [Pg.58]    [Pg.329]    [Pg.338]    [Pg.341]    [Pg.361]    [Pg.163]   
See also in sourсe #XX -- [ Pg.6 ]




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