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Biomolecules chemistry

Various applications of NMR in biochemistry include structural identification of biomolecules, chemistry of individual groups in macromolecules, structural and dynamic information of biomacromolecules, metabolic studies, and kinetic and association constants of ligand bindings to macromolecules (Wiithrich, 1986). [Pg.87]

Many computational chemistry techniques are extremely computer-intensive. Depending on the type of calculation desired, it could take anywhere from seconds to weeks to do a single calculation. There are many calculations, such as ah initio analysis of biomolecules, that cannot be done on the largest computers in existence. Likewise, calculations can take very large amounts of computer memory and hard disk space. In order to complete work in a reasonable amount of time, it is necessary to understand what factors contribute to the computer resource requirements. Ideally, the user should be able to predict in advance how much computing power will be needed. [Pg.128]

Indeed, cellular constituents or biomolecules must conform to the chemical and physical principles that govern all matter. Despite the spectacular diversity of life, the intricacy of biological structures, and the complexity of vital mechanisms, life functions are ultimately interpretable in chemical terms. Chemistry is the lo e of biolo eal phenomena. [Pg.3]

Continuing our look at the four main classes of biomolecules, we ll focus in this chapter on amino acids, the fundamental building blocks from which the 100,000 or so proteins in our bodies are made. We ll then see how amino acids are incorporated into proteins and the structures of those proteins. Any understanding of biological chemistry would be impossible without this study. [Pg.1017]

Modular Presentation Topics are arranged in a roughly modular way. Thus, certain chapters are grouped together simple hydrocarbons (Chapters 3-8), spectroscopy (Chapters 12-14), carbonyl-group chemistry (Chapters 19-23), and biomolecules (Chapters 25-29). 1 believe that this organization brings to these subjects a cohesiveness not found in other texts and allows the instructor the flexibility to teach in an order different from that presented in the book. [Pg.1336]

Chapter 28, Biomolecules Nucleic Acids—Coverage of heterocyclic chemistry has been moved to Chapter 24. [Pg.1337]

Some of their derivatives have been used as antiviral drugs. Due to their flexible chemistry, they can be exploited to design drug delivery systems and in molecular nanotechnology. In such systems, they can act as a central lipophilic core and different parts like targeting segments, linkers, spacers, or therapeutic agents can be attached to the said central nucleus. Their central core can be functionalized by peptidic and nucleic acid sequences and also by numerous important biomolecules. [Pg.248]

Simmonds, R. J. (1992), Chemistry of Biomolecules - an Introduction, Royal Society of Chemistry, London. [Pg.615]

The dansyl derivative 9-azidononyl-5-(dimethylamino)naphthalene-l-sulfonate 35 was used by Yi and collaborators [91] as an azido-fluorescent label in a tandem method of sulfonium alkylation and click chemistry for the modification of biomolecules. Fluorescent labeling of a protein was successfully carried out after simple incubation of BSA with sulfonium salt 36 followed by azido-containing fluorophore 35, at room temperature. [Pg.40]

The compound HCN occupies a position at the border between inorganic and organic chemistry. It is paradoxical that hydrogen cyanide is on the one hand an important starting material for prebiotic syntheses of biomolecules and on the other a deadly poison for living organisms. [Pg.104]

The process known as SPREAD (Surface Promoted Replication and Exponential Amplification of DNA Analogues) attempts to reach the target, striven for by many researchers, of an exponential proliferation of biomolecules in model systems. As already mentioned, product inhibition (e.g., by dimerisation of the new matrices to give C2) only allowed parabolic growth. In the SPREAD process, both solid phase chemistry and feeding have a positive effect on the synthesis. Thus, no separation processes are required, as excess reagents can be removed just by washing. The synthetic process consists of four steps ... [Pg.159]

The thioester world postulated by de Duve should in fact be called the sulphur-iron world , since iron ions are essential for the redox processes occurring in such a thioester world, de Duve (1991, 1996) asks a question which is vital for the whole of prebiotic chemistry where did the redox equivalents necessary for the construction of biomolecules on the primeval Earth come from This question becomes largely irrelevant if the strongly reducing atmosphere postulated by Miller/Urey and... [Pg.204]

The processes occurring at hydrothermal systems in prebiotic periods were without doubt highly complex, as was the chemistry of such systems this is due to the different gradients, for example, of pH or temperature, present near hydrothermal vents. Studies of the behaviour of amino acids under simulated hydrothermal conditions showed that d- and L-alanine molecules were racemised at different rates the process was clearly concentration-dependent. L-Alanine showed a low enantiomeric excess (ee) over D-alanine at increasing alanine concentrations. The same effect was observed with metal ions such as Zn2+ in the amino acid solution. Thus, homochi-ral enrichment of biomolecules in the primeval ocean could have resulted under the conditions present in hydrothermal systems (Nemoto et al., 2005). [Pg.252]

Aurora Biomolecules dedicates to peptide synthesis (and polyclonal antibody production) for any small quantity purpose. FMOC chemistry (on Perceptive Biosystems Pioneer instruments) is used for peptides synthesis Online monitoring of the coupling efficiencies and HATU activation helps insure that the major component of the synthesis is the correct oligopeptide. Purification is firstly carried out by size exclusion chromatography, and then by HPLC on a PE vision purification workstation. Typically, 20 mg of pure peptide are obtained. The molecular weight of the purified peptide is determined as a final confirmation of quality. [Pg.234]


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