Sourcing strategy matrix

With the matrix as a guide to strategy, tactics must be applied to implement the purposes of the matrix. Figure 3.5 provides a model that matches the five levels of the supply chain progression with the type of tactics that are typical as a sourcing strategy matures. The tactics placed in each sector of the progression are what typically takes place, but a firm is advised to construct its own list of tactics pertinent to local conditions. 

Alternatively (or initially) the mixture is treated as a whole and tested in its crude state. The advantage of this strategy includes the relevancy of the tested sample to its environmental counterpart, decreased potential for artefact formation, and inclusion of combined effects of chemicals in the mixture. Moreover if the mixture is representative of others in its class (e.g., diesel emissions from different sources would share certain characteristics), it may be possible to extrapolate results across samples. This method also circumvents the labor-intensive process of individual testing of multiple chemicals. But sometimes a complex mixture is too cytotoxic to be tested directly in a bioassay. Furthermore, it may be incompatible with the test system because of the physical matrix. Other disadvantages include the inability to specify the constituent of the mixture responsible for the toxicity, as well as potential masking effects (e.g., the masking of mutagenicity by cytotoxicity). 

Second, contraptions used for external generation of reactive intermediates are often quite bulky, which may impede the mobility of the experiment. Such contraptions may render it difficult to investigate a sample by several different kinds of spectroscopy. In principle it is possible, with the aid of a gate valve mounted on the vacuum shroud, to construct devices that allow one to retract and detach the external source of a reactive intemediate after a matrix has been built, but the implementation of this strategy is technically quite challenging because high vacuum must be maintained at all times within the cryostat. 

These direct ion sources exist under two types liquid-phase ion sources and solid-state ion sources. In liquid-phase ion sources the analyte is in solution. This solution is introduced, by nebulization, as droplets into the source where ions are produced at atmospheric pressure and focused into the mass spectrometer through some vacuum pumping stages. Electrospray, atmospheric pressure chemical ionization and atmospheric pressure photoionization sources correspond to this type. In solid-state ion sources, the analyte is in an involatile deposit. It is obtained by various preparation methods which frequently involve the introduction of a matrix that can be either a solid or a viscous fluid. This deposit is then irradiated by energetic particles or photons that desorb ions near the surface of the deposit. These ions can be extracted by an electric field and focused towards the analyser. Matrix-assisted laser desorption, secondary ion mass spectrometry, plasma desorption and field desorption sources all use this strategy to produce ions. Fast atom bombardment uses an involatile liquid matrix. 

In this study, we used matrix-assisted laser desorption ionization /Mass Spectrometry (MALDI/MS) to identify the peptides released from gastric parietal cell microsomes. MALDI, because of its sensitivity and relative tolerance to the presence of salts and buffers was examined for the analysis of unfractionated proteolytic digests (9, 10). MALDI with post-source decay (PSD) analysis was used to obtain sequence information on peptides even in crude digestion mixtures. Our strategy (Figure 1) consisted of proteolysis of intact vesicles, centrifugation at high speeds to separate membrane bound and soluble fractions and analysis of the mixture of released peptides by MALDI/MS. In addition, to increase the... 

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