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Polypeptides synthesis and

Polypeptide Synthesis and Analysis. Sihca or controUed-pore glass supports treated with (chloromethyl)phenylethyltrimethoxysilane [68128-25-6] or its derivatives are replacing chloromethylated styrene—divinylbenzene (Merrifield resin) as supports in polypeptide synthesis. The sdylated support reacts with the triethyl ammonium salt of a protected amino acid. Once the initial amino acid residue has been coupled to the support, a variety of peptide synthesis methods can be used (34). At the completion of synthesis, the anchored peptide is separated from the support with hydrogen bromide in acetic acid (see Protein engineering Proteins). [Pg.73]

Note Presented here is a summary of data from one of the early experiments designed to elucidate the genetic code. A synthetic RNA containing only A and C residues in a 5 1 ratio directed polypeptide synthesis, and both the identity and the quantity of incorporated amino acids were determined, Based on the relative abundance of A and C residues in the synthetic RNA, and assigning the codon AAA (the most likely codon) a frequency of 100, there should be three different codons of composition A2C, each at a relative frequency of 20 three of composition AC2, each at a relative frequency of 4,0 and CCC at a relative frequency of 0.8. The CCC assignment was based on information derived from prior studies with poly(C), Where two tentative codon assignments are made, both are proposed to code for the same amino acid. [Pg.1037]

Initiation factors contribute to the ribosome complex with the messenger RNA and the initiator methionyl-tRNA. Elongation factors assist the binding of all the other tRNAs and the translocation reaction that must occur after each peptide bond is made. Termination factors recognize a stop signal and lead to the termination of polypeptide synthesis and the release of the polypeptide chain and the messenger from the ribosome. [Pg.765]

The elongation phase of polypeptide synthesis and its termination are described in Example 17.8. The A site is shown to be filled by AA2-tRNA where the codon xxx is located. [Pg.504]

Also see color figure.) Hepatic vitamin K metabolism. Oral anticoagulant drugs act indirectly on the process of glu carboxylation of the vitamin K dependent proteins. The vitamin K antagonists block the reduction of the reaction intermediate, vitamin K-epoxide, that results in the accumulation of vitamin K-epoxide and other nonfunctional forms of vitamin K. Without cycling of the vitamin K-related reaction intermediates in the cycle shown, a depletion of functional vitamin K occurs. Vitamin K antagonists do not block polypeptide synthesis and formation of noncarboxylated proteins occurs. These noncarboxylated proteins are still secreted from the liver and account for nearly normal levels of each of the vitamin K-dependent proteins that can be detected by immunoassay (sometimes called PIVKA, proteins induced in vitamin K absence). [Pg.863]

Read GS, Frenkel N (1983) Herpes simplex virus mutants defective in the virion-associated shutoff of host polypeptide synthesis and exhibiting abnormal synthesis of alpha (immediate early) viral polypeptides. J Virol 46 498-512... [Pg.184]

Termination codon, stop codon, punctuation codon a sequence of three nucleotides in mRNA, which signals the end of polypeptide synthesis and release of the polypeptide in the process of Protein biosynthesis (see). 5 -tlAA (see Ochre codon), 5 -UAG (see Amber codon) and UGA are T.c. [Pg.664]

M. Ligeti, G. Mezo, K. Marko, E. Madarasz and F. Hudecz, Conjugation of a cyclic rgd derivative to branched chain polymeric polypeptide Synthesis and biological study of AK-(cyclo[RGDfC])),/. Peyt. Sci., 12,178 (2006). [Pg.65]

Peterkofsky, B., 1972, The effect of ascorbic acid on collagen polypeptide synthesis and proline hydroxy lation during the growth of cultured fibroblasts. Arch. Biochem. Biophys. 152 318-328. [Pg.106]

The first three sections of this chapter deal with addition polymerization, the fourth with condensation polymerization, the fifth with kinetics of the syntheses of polymers, the sixth with polypeptide synthesis, and the seventh with nucleic acid synthesis. Readers should be familiar with these subjects before going on to the major topics of this book. The chapter itself could be considered as a book in miniature on synthetic chemistry. Important synthetic methods and well-known chemical compounds are covered. [Pg.19]


See other pages where Polypeptides synthesis and is mentioned: [Pg.128]    [Pg.1038]    [Pg.757]    [Pg.87]    [Pg.415]    [Pg.338]    [Pg.49]    [Pg.1038]    [Pg.577]    [Pg.316]    [Pg.71]    [Pg.85]    [Pg.459]    [Pg.274]    [Pg.660]    [Pg.386]    [Pg.399]    [Pg.79]    [Pg.314]    [Pg.48]    [Pg.172]   
See also in sourсe #XX -- [ Pg.1193 , Pg.1194 ]




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Oligo- and Polypeptide Synthesis

POLYPEPTIDE SYNTHESIS AND CLEAVAGE

Polypeptide and Protein Synthesis

Polypeptide synthesis

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