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Other Initiation Factors

Besides eIF-2, the 40 S/Met-tRNAf complex that binds to mRNA also contains all the polypeptides of eIF-3 and eIF-4C (see Section [Pg.118]

Omission of eIF-4C causes only a marginal reduction in the binding of mRNA (Benne and Hershey, 1978). On the other hand, binding of mRNA is stimulated by eIF-3 and by two other initiation factors, eIF-4A and eIF-4B (Trachsel et ai, 1977 Benne and Hershey, 1978), and it requires the hydrolysis of ATP (Marcus, 1970 Trachsel et al., 1977 Benne and Hershey, 1978). [Pg.119]

Curiously, eIF-4A, eIF-4B, and eIF-4F stimulate translation of the uncapped STNV RNA to the same extent as that of globin mRNA (Grifo et al., 1983), indicating that, conceivably, they interact with other features in mRNA besides the cap. Indeed, translation of the [Pg.119]

The data available as of summer 1983 indicate that the number of different polypeptide chains involved, besides eIF-2, in binding of mRNA may be more limited than would seem, as the various complexes or chains designated as eIF-3, eIF-4A, eIF-4B, eIF-4F (CPB-II), and 24-CBP possess extensive structural and functional relationships and thus may be different, and possibly artifactual, derivatives of a simpler set of proteins. [Pg.121]

No sequence studies of the interaction of these proteins with mRNA have yet been reported, and specific binding to a region in mRNA remains to be demonstrated. On the basis of the available data, it is tempting to suggest that eIF-2 recognizes the sequence and conformation around the initiation site in mRNA, while the above-mentioned proteins may unwind secondary structure in mRNA and anchor it at the 5 -terminal cap structure. [Pg.121]


The GTPase-catalysed cycle of the initiation of protein synthesis involves the formation of the small (30S or 40 ) ribosomal subunit initiation complex and its subsequent binding to the large (405 or 605) ribosomal subunit. In this process the initiation factor (IF-2 or eIF-2), in association with GTP, facilitates the appropriate association of the ribosomal subunit, mRNA, fMet- or Met-tRNA and other initiation factors to form the initiation complex which then binds to the large ribosomal subunit, an event that triggers the hydrolysis of GTP and the release of the initiation factors. Although it is not clear what plays the role of GEP in this cycle, the large ribosomal subunit appears to function as GAP. [Pg.268]

Thus, we would suggest that the immediate upstream sequences either provide a mechanism for the polymerase and other initiation factors to initially bind the DNA, after which they must scan along... [Pg.76]

The ternary complex is an obligatory intermediate for the binding of Met-tRNAf to the 40 S ribosomal subunit. The ternary complex binds readily to the 40 S subunit in the absence of mRNA, and this binding is stable in sucrose gradients (Benne et al., 1976 Trachsel et al., 1977 Peterson et al., 1979). The binding is stimulated in the presence of eIF-3 and eIF-4C, probably because these factors stabilize the resulting complex. Using radioactive factors, the presence in the 40 S/Met-tRNAf/GTP complex of all of the subunit polypeptides of eIF-2, eIF-3, and eIF-4C, but no other initiation factors, could be demonstrated (Benne and Hershey, 1978 Peterson et al., 1979). [Pg.111]

Trachsel et al. (1980) hypothesized that during the course of poliovirus infection, the CBP is inactivated. As a result, uncapped viral mRNAs are translated, but capped host mRNAs are not translated. Recent studies indicate that poliovirus infection leads to the inability of CBP to form active complexes with other initiating factors, thereby causing an inhibition of capped mRNA entry into initiation complexes (Brown et al., 1982 Hansen et al., l9S2a,b). [Pg.446]

The decomposition kinetics of an organic peroxide, as judged by 10-h HLT, largely determines the suitabiUty of a particular peroxide initiator in an end use appHcation (22). Other important factors ate melting point, solubiUty, cost, safety, efficiency, necessity for refrigerated storage and shipment, compatibihty with production systems, effects on the finished product, and potential for activation. [Pg.135]

Such products were observed more or less in the polymerization with other initiators (S11CI4, SbCls, CH3COBF4, Et30BF4, and EtOSC F). These phenomena are inconsistent with a usual equilibrium process if, as expected, the enthalpy of the polymerization is negative. Therefore, solubility and kinetic factors must play an important role. [Pg.66]

Two initiation factors, eIF-3 and elF-lA, bind to the newly dissociated 40S ribosomal subunit. This delays its reassociation with the 60S subunit and allows other translation initiation factors to associate with the 40S subunit. [Pg.365]

In the case when one of the two measurements of the contingency table is divided in ordered categories, one can construct a so-called thermometer plot. On this plot we represent the ordered measurement along the horizontal axis and the scores of the dominant latent vectors along the vertical axis. The solid line in Fig. 32.9 displays the prominent features of the first latent vector which, in the context of our illustration, is called the women/men factor. It clearly indicates a sustained progress of the share of women doctorates from 1966 onwards. The dashed line corresponds with the second latent vector which can be labelled as the chemistry/ other fields factor. This line shows initially a decline of the share of chemistry and a slow but steady recovery from 1973 onwards. The successive decline and rise are responsible for the horseshoe-like appearance of the pattern of points representing... [Pg.198]

The goals of most LCA have been limited to determination of the impact of the fluid milk process on GHG emissions and energy due to the availability of relevant data and guidelines from the IPCC and other government agencies. Data for conducting LCA of the other impact factors such as water use, aquatic toxicity, human health, and land use are scarce, but new initiatives to reduce the impact of dairy production in... [Pg.47]

Viral IRES elements can be useful tools to identify the sub-step in translation targeted by a given regulator (Jackson, 2005 Ostareck et al., 2001). The IRES elements listed in Table 6.1 are of particular interest, because careful biochemical and structural analyses have defined different initiation factor requirements for translation in each case (Borman and Kean, 1997 Fraser and Doudna, 2006 Hellen and Sarnow, 2001 Poyry et al, 2004). We and others have employed viral IRES-containing reporter constructs to... [Pg.125]

Recently, we analyzed the role of electron repulsion relative to bond breaking and antiaromaticity effects on a quantitative basis using Natural Bond Orbital (NBO) analysis.24 Two other destabilizing factors were considered at the initial stage of the cyclization in addition to four-electron repulsion between the filled in-plane acetylenic re-orbitals - distortion/breaking of the acetylenic bonds as a result of their bending, and the fact that, at a distance of ca. 3 A, the in-plane re-orbitals become parallel and reach a geometry that resembles the antiaromatic TS of the symmetry forbidden [2S + 2S] cycloaddition (vide infra). [Pg.11]

Cyclic voltammetry was used to monitor the mechanism for (TPP)Rh(R) formation according to Equation 3 where RX is a terminal alkyl halide. The current for reduction of electrogenerated (P)Rh(R) or (P)Rh(RX) species is a measure of the concentration of this product at the electrode surface, and hence a measure of its rate of formation. The current must be standardized for experimental factors such as scan rate, initial concentration of [(TPP)Rh(L)J+cr (or other initial Rh(III) species), electrode area, and concentration of the alkyl halide reactant. [Pg.456]


See other pages where Other Initiation Factors is mentioned: [Pg.1058]    [Pg.374]    [Pg.520]    [Pg.520]    [Pg.1058]    [Pg.118]    [Pg.128]    [Pg.152]    [Pg.1058]    [Pg.374]    [Pg.520]    [Pg.520]    [Pg.1058]    [Pg.118]    [Pg.128]    [Pg.152]    [Pg.325]    [Pg.250]    [Pg.39]    [Pg.910]    [Pg.633]    [Pg.172]    [Pg.208]    [Pg.120]    [Pg.848]    [Pg.950]    [Pg.1106]    [Pg.133]    [Pg.182]    [Pg.495]    [Pg.324]    [Pg.378]    [Pg.77]    [Pg.148]    [Pg.292]    [Pg.303]    [Pg.503]    [Pg.448]    [Pg.473]    [Pg.126]    [Pg.53]    [Pg.78]    [Pg.85]    [Pg.208]    [Pg.102]   


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