Peptide And Protein Synthesis Research References

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1 Peptide And Protein Synthesis Research References Altmann M, Muller P, and Trachsel H. (1993) A S. cerevisiae homologue of mammalian translation initiation factor 4B contributes to RNA helicase activity. EMBO J. 12: Aravind L, and Koonin E. (2001) Eukaryote-specific domains in translation initiation factors: Implications for translation regulation and evolution of the translation system. Gen. Res. Bartig D., Lemkeier K., Frank J., and Klink F. (1992) The archaebacterial hypusinecontaining protein: structureal features suggest common ancestry with eukaryotic translation initiation factor 5A. Eur. J. Biochem. 204: Battiste J., Pestova T., and Hellen C. (1995) The eif1a solution structure reveals a large RNA-binding surface important for scanning function. Mol. Cell 5: Castilho B., and Donahue T. (1992) Mutation analysis of the Cys-X-Cys-X-Cys-C-Cys motif in the beta subunit of eukaryotic translation initiation factor 2. Gene expression 2: Cazzola M., and Skoda R. (2000) Translational pathophysiology: a novel mechanism of human disease. Blood 95: Cigan A., Feng L., and Donahue T. (1998) Initiator trna functions in directing the scanning ribosome to the start site of translation. Science 242:93 Cigan A., Pabich E. and Donahue T. (1989) Yeast translation initiation suppressor sui2 encodes the alpha subunit of eukaryotic initiation factor 2 and share sequence identity with the human alpha subunit. PNSA 86: Chakrabarti A. and Maitra U. (1991) Function of eukaryotic initiation factor 5 in the

2 formation of an 80S ribosomal polypeptide chain initiation complex. J. Biol. Chem. 266: Craig AW, Haghighat A, Yu AT, Sonenberg N. (1998) Interaction of polyadenylatebinding protein with the eif4g homologue PAIP enhances translation. Nature. Apr 2:392 (6675): Danaie P., Wittmer B., Altmann M., and Trachsel H. (1995) Isolation of a protein complex containing translation initiation factor Prt1 from Saccharomyces cerevaisiae. J. Biol. Chem. 270: Dever T., Wei C and Hershey J. (1994) Determination of the amino acid sequence of rabbit, human and wheat germ protein synthesis factor eif-4c by cloning and chemical sequencing. J. Bio. Chem. 269: Donahue T., Cigan A., and Catilho B. (1998) Mutations at a Zn(II) finger motif in the yeast eif-2beta gene alter ribosomal start-site selection during the scanning process. Cell 54: Dorris D., Erickson F., and Hannig E. (1995) Mutations in GCD11, the structural gene for eif2-gamma in yeast, after translational regulation of GCN4 and the selection of the start site for protein synthesis. EMBO J. 14: Dube P., Wieske M., Startk., and Zemlin F. (1998) Correlation of the expansion segments in mammalian rrna with the fine structure of the 80S ribosome: a cryoelectron microscopic reconstruction of the rabbit reticulocyte ribosome at 21 angostroms resolution. J. Mol. Biol. 279: Erickson F., Harding L., Dorris D., and Hanning E. (1996) Ligand interactions with the eukaryotic translation initiation factor 2: role of the gamma-subunit. EMBO J. 15: Fletcher C., Pestova T., and Hellen C. (1999) Structure and interaction of translation

3 initiation factor eif1. EMBO J. 18: FlynnA., Shatsby I., Proud C., and Kaminski A. (1994) The RNA-binding properties of protein synthesis initiation factor eif-2. Biochim. Biophys. Acta. 1219: Furuichi Y., and K-I Miura. (1975) A blocked structure at the 5 terminus of mrna from cytoplasmic polyhedrosis virus. Nature 253: Furuichi et al. (1997) 5 -terminal structure and mrna stability. Nature Gallie, DR. (1991) The cap and poly(a) tail function synergistically to regulate mrna translational efficiency. Genes Dev. 5: Gerbi SA. (1996) Expansion segments: regions of variable size that interrupt the universal core secondary structure of ribosomal RNA. In: Ribosomal RNA: Structure, Evolution, Processing and Function in Protein Biosynthesis. CRC, New York Gorbalenya A., and Koonin E. (1993) Helicases: amino acid sequence comparisons and structure-function relationships. Curr/ Opin. Struc. Biol. 3: Jackson RJ. (1991) RNA translation. Initiation without an end. Nature 353(6339):14-15 Konarska M., Filipowicz W., and Gross H. (1981) Binding of ribosomes to linear and circular forms of the 5 -terminal leader fragment of tobacco mosaic virus RNA. Eur. J. Biochem. 114:221 Kozak M., and Shatkin A. (1978) Migration of 40S ribosomal subunits on mrna in the presence of edeine. J. Biol. Chem. 253: Kozak M. (1979) Inability of circular mrna to attach eukaryotic ribosomes. Nature 280:82 Kozak M. (1980) Role of ATP in binding and migration of 40S ribosomal subunits. Cell 22:971

4 Kozak M. (1983) Translation of insulin-related polypeptides from messenger RNAs with tandemly reiterated copies of the ribosome binding site. Cell 34:971 Kozak M. (1986) Influences of mrna secondary structure on initiation by eukaryotic ribosomes. PNAS 83: 2850 Kozak M. (1989) The scanning model for translation: an update. J. Cell. Biol. 9: 5134 Kozak M. (1991) Structural features in eukaryotic mrnas that modulate the initiation of translation. J. Biol. Chem. 266: Kozak M. (1992) Circumstances and mechanisms of initiation of translation by secondary structure in eukaryotic mrnas. Review Mol. Cell. Biol. 9:5134 Kozak M. (1995) Adherence to the first-aug rule when a second AUG codon follows closely upon the first. Proc. Natl. Acad. Sci. 92:7134 Kozak M. (1992) A consideration of alternative models for the initation of translation in eukaryotes. Mole. Biol. 27: Kozak M. (1992) A consideration of alternative models for the initiation of translation in eukaryotes. Crit. Rev. Biochem and Mol. Bio. 27: Kozak M. (1999) Initiation of translation in prokaryotes and eukaryotes. Review Gene 234: Kyripides N. and Woese C. (1998) Universally conserved translation initiation factors. RNAS 95: La Teana A., Pon C., and Gualezrzi C. (1996) Late events in translation initiation: adjustment of initiatior trna in the ribosomal P site. J. Mol. Biol. 256: Lawrence C., Abraham R. (1997) PHAS-4E-BPs as regulators of mrna translation and cell proliferation. Trends in Biochem. Sci. 22:

5 Lawson T., Lee K., Maimone M., and Merrick W. et al. (1989) Dissociation of doublestranded polynucleotide helical structures by eukaryotic initiation factors, as revealed by a novel assay. Biochemistry 28: Le H., Tanguay R., Balesta M., et al. (1997) The translation initiation factors eifiso4g and eif4b with the poly(a) binding protein to increase its RNA binding affinity. J. Biol. Chem. 272: Marcotrigiano J., Gingras A., and Burley S. (1997) Cocrystal structure of the messenger RNA 5 cap-binding protein (eif4e) bound to 7-methyl-GDP. Cell 89: Marcotrigiano J., Gingras A., and Burley S. (1999) Cap-dependent translation intiation in eukaryotes is regulated by molecular mimic of eif 4G. Mol. Cell. 3: Marcotrigiano J., Lomakin IB., Sonenberg N., Pestova TV., et al. (2001) A conserved HEAT domain within eif4g directs assembly mrnas as initiation factor eif-4b. Arch. Biochem Biophys. 276:6 Molecular Biology (1999) Weaver, Robert Frank. The McGraw-Hill Companies, Inc. (USA) Morgan D., et al. (2000) A comparison of the yeast and rabbit 80S ribosome reveals the topology of the nascent chain ext tunnel, inter-subunit bridges and mammalian rrna expansion segments. J. Biol. Chem. 301: Muller PP, Trachsel H. Translation and regulation of translation in the yeast Saccharomyces cerevisiae. Eur. J. Biochem : Review Munroe D. and Jacobson A. (1990) mrna poly(a) tail, a 3 enhanced of translaitonal initiation. Mol. Cell. Biol. 10:3441 Naranda T., Kainuma M., et al. (1997) The 39-kilodalton subunit of eukaryotic translation initation factor 3 is essential for the complex s integrity and cell viability in Saccharonyces cerevisiae. Mol. Cell. Biol.

6 Naranda T., et al (1994) Two structural domains of initiation factor eif-4b are involved in binding RNA. J. Biol. Chem. 269: Otero J., Ashe M., et al. (1999) The yeast poly(a)-binding protein Pab1p stimulates in vitro poly(a)-dependent and cap-dependent translation by distinct mechanisms. EMBO J. 18: Pause A., and Sonenberg N. (1992) Mutational analysis of a DEAD box RNA helicase: the mammalian translation initiation factor eif-4a. EMBO J. 11: Pestova T., et al. (1998) Eukaryotic ribosomes require initiation factors 1 and 1A to locate initiation codons. Nature 394: Pestova T., et al. (2000) The joining of ribosomal subunits in eukaryotes requires eif5b. Nature 403: Pestova T., et al. (2000) The structure and function of initiation factors in eukaryotic protein synthesis. Review. Cell Mol. Life Sci. 57: Piron M, et al. (1998) Rotavirus RNA-binding protein NSP3 interacts with eif4gi and evicts the poly(a) binding protein from eif4f. EMBO J. 17: Preiss T., Hentze M.W. From factors to mechanisms: translation and translational control in eukaryotes. Curr. Opin. Genet. Dev. 5: Review. Price N., Kimball S., et al. (1996) Cloning of cdna for the gamma subunit of mammalian translation initiation factor 2B, the guanine-exchange factor for the eukaryotic initiation factor 2. Biochem. J. 318: Raychaudhuri P., et al. (1985) Eukaryotic initiation factor 5 from calf liver is a single polypeptide chain of Mr=62,000. J. Biol. Chem. 260: Rahul C., et al. (1999) Recognition of polyadenylate RNA by the poly(a)-binding protein. Cell 98:

7 Rhoads R.E. (1993) Regulation of eukaryotic protein synthesis by initiation factors. J. Biol. Chem. 268: Rozen F., et al. (1990) Bidirectional RNA helicase activity of eukaryotic translation initiation factors 4A and 4F. Mol. Cell Biol. 10: Sachs A., Sarnow P., et al. (1997) Starting at the beginning, middle and end: translation initiation in eukaryotes. Cell 89: Sallaas M. (1999) Internal ribosome entry site biology and its use in expression vestors. Curr. Op. Biol. 10: Sanvito F., Piatti S., Villa A. et al. (1999) The beta4 integrin interactor p27 is an essential nuclear matrix protein involved in 60S ribosomal subunit assembly. J. Cell Biol. 144: Schmid S., and Linder P. (1991) Translation initiation factor 4A from S. cerevisiae: analysis of residues conserved in the DEAD family of RNA helicases. Mol. Cell Biol. 11: Sette M, Spurin R., et al. (1997) The structure of the translational initiation if1 from E.coli contains an oligomer-binding motif. EMBO J. 16: Sutrave P., Schafer B., et al. (1994) Isolation, identification and characterization of the FUN12 gene S.cerevisiae. Gene 146: Trachsel H. (1996) Binding of initiator trna to ribosomes. Cold Spring Harbor Press pp Van Heutgen H., Kasperaitis M., et al. (1991) Evidence that eif-2 is a cap-binding protein that stimulates cap recognition by eif-4b and eif-4f. J. Biol. Chem. 266:7229 Vershoor A., Srivastava S., and Frank J. (1996) Native 3D structure of eukaryotic 80S ribosome: morphological homology with the E.coli 70S ribosome. J. Cell Biol. 133:495-

8 505 Wei, C.L., Kainuma, M., and Hershey J. (1995) Protein synthesis initiation factor eif-1a is a moderately abundant RNA-binding protein. J. Biol. Chem. Wei N., and Deng, X. (1999) Making sense of the COP9 signalosome. A regulatory protein complex conserved from Abrabidopsis to human. Trends Genet. 15: Wei C., MacMillan S., and Hershey J. (1995) Protein synthesis initiation factor eif-1a is a moderately abundant RNA-binding protein. J. Biol. Chem. 270: Wilson A., and Noller H. (1998) Molecular movement inside the translational engine. Cell 92: Wool I., Chan Y., and Gluck A. (1996) Mammalian ribosomes: the structure and the evolution of proteins. In: Translational Control. Cold Springs Laboratory Press Yoon H., and Donahue T. (1992) The suil suppressor locus in Saccharomyces cerevisiae encodes a translation factor the functions during initiator trna recognition of the start codon. Mol. Cell Biol. 12: Zuk D., and Jacobson A. (1998) A single amino acid substitution in yeast eif-5a results in mrna stabilization. EMBO J.17: Click here for more information about our custom peptide synthesis services

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