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Protein general considerations

DENATURATION OF INDIVIDUAL MILK PROTEINS General Considerations... [Pg.587]

Computer simulations of electron transfer proteins often entail a variety of calculation techniques electronic structure calculations, molecular mechanics, and electrostatic calculations. In this section, general considerations for calculations of metalloproteins are outlined in subsequent sections, details for studying specific redox properties are given. Quantum chemistry electronic structure calculations of the redox site are important in the calculation of the energetics of the redox site and in obtaining parameters and are discussed in Sections III.A and III.B. Both molecular mechanics and electrostatic calculations of the protein are important in understanding the outer shell energetics and are discussed in Section III.C, with a focus on molecular mechanics. [Pg.395]

On the basis of general considerations, it is quite evident that the chemical synthesis of protein-like HP-copolymers can be performed by using one of the following three different methods ... [Pg.102]

Schoenberg R, Zink S, Staubwasser M, von Blanckenburg F (2008) The stable Crisotope inventory of solid Earth reservoirs determined by double-spike MC-ICP-MS. Chem Geol 249 294-306 Schoenheimer R, Rittenberg D (1939) Studies in protein metabolism I, General considerations in the application of isotopes to the study of protein metabolism. The normal abundance of nitrogen isotopes in amino acids, J Biol Chem 127 285-290... [Pg.268]

The combination of the two processes is generally only carried out when the amount of protein available is limited they require very different quantities of material thus, the diamino acids can be determined in 25 to 50 grammes of protein with considerable accuracy, whereas the monoamino acids can only be determined with fair accuracy when 250 to 500 grammes of protein can be used. On the whole, it is not... [Pg.18]

From a chemical point of view, the half-life of fluorine-18 allows multi-step synthetic approaches that can be extended over hours. Fluorine-18 has therefore, in spite of its somewhat limited chemical repertoire, been effectively used for the labelling of numerous both relatively simple and complex bioactive chemical structures [3,5-9], including high-molecular-weight macromolecules such as peptides, proteins [10-13] and oligonucleotides [14-18]. General considerations on radiochemistry involving short-lived positron emitters will be discussed in Section 2.3. [Pg.6]

For rationally constructing domain-swapped proteins, one consideration is whether to include a linker region between the two domains. In general, hybrids with two autonomously functioning domains require significant distance between the two domains so that they can fold and... [Pg.59]

Peptides Peptides, similar to proteins, consist of amino acids, although their molecular weights are lower than those of proteins. Therefore the considerations above for proteins are also applicable to peptides. Antibody formation, which is a key issue in animal experiments on human-type proteins, generally depends on molecular weight (i.e., the probability of antibody formation is low if the molecular weight is low). The guideline covers not only biotechnologi-cally produced peptides but also chemically synthesized peptides. [Pg.102]

General Considerations. The nitrogenase enzyme consists of two separately isolable proteins—the molybdenum-iron protein (Component I, Fraction I, molybdoferredoxin) and the iron protein (Component II, Fraction II, azoferredoxin). The most recent work on nitrogenase com-... [Pg.357]

It is still not fully understood why the tyrosyl radical in protein R2 is so stable. In E. coli R2 stored at 4 C the radical remains for weeks, and stored at fi80 C for years (Sahlin et al., 1989). Even though the lifetime of the radical varies considerably in preparations of R2 from different species, especially when handled above 0 C, the radical in these R2 proteins generally withstands low temperature storage well. [Pg.431]

The main general consideration that can be stated so far is 1) the smoothness of the separations 2) the absence of cell prelabeling and 3) the development of biocompatible instrumentation, which allows subpopulation lineage to be produced, which are not only usable for fundamental studies such as differentiation pathways or apoptosis studies, but also for transplantation or genetic engineering. One must have in mind that the cell is definitively the place, home, and native localization of genes and proteins. The possibility of rapid, nondestructive separation, purification, and characterization of cells (cellulomics) opens fabulous dimensions for proteomics and genomics. [Pg.331]


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See also in sourсe #XX -- [ Pg.587 ]




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