Transcending the impenetrable: how proteins come to terms with membranes.
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[1] F. Hartl,et al. Successive translocation into and out of the mitochondrial matrix: Targeting of proteins to the intermembrane space by a bipartite signal peptide , 1987, Cell.
[2] K. Ito,et al. Topology analysis of the SecY protein, an integral membrane protein involved in protein export in Escherichia coli. , 1987, The EMBO journal.
[3] G. Shore,et al. The interaction of a synthetic mitochondrial signal peptide with lipid membranes is independent of transbilayer potential. , 1987, The EMBO journal.
[4] A. Kuhn,et al. The internal signal sequence of Escherichia coli leader peptidase is necessary, but not sufficient, for its rapid membrane assembly. , 1987, The Journal of biological chemistry.
[5] E. D. De Robertis,et al. The nuclear migration signal of Xenopus laevis nucleoplasmin. , 1987, The EMBO journal.
[6] M. Spiess,et al. Deletion analysis of the internal signal‐anchor domain of the human asialoglycoprotein receptor H1. , 1987, The EMBO journal.
[7] R. Kelly,et al. In vitro mutagenesis of trypsinogen: role of the amino terminus in intracellular protein targeting to secretory granules , 1987, The Journal of cell biology.
[8] K. Furtak,et al. The ornithine transcarbamylase leader peptide directs mitochondrial import through both its midportion structure and net positive charge , 1987, The Journal of cell biology.
[9] D. Blank,et al. Transport of proteins to the mitochondrial intermembrane space: the ‘matrix‐targeting’ and the ‘sorting’ domains in the cytochrome c1 presequence. , 1987, The EMBO journal.
[10] K. Mihara,et al. A short amino‐terminal segment of microsomal cytochrome P‐450 functions both as an insertion signal and as a stop‐transfer sequence. , 1987, The EMBO journal.
[11] G. Schatz,et al. Import of an incompletely folded precursor protein into isolated mitochondria requires an energized inner membrane, but no added ATP. , 1987, The EMBO journal.
[12] W. Richardson,et al. The effect of protein context on nuclear location signal function , 1987, Cell.
[13] R. Gentz,et al. A functional interaction between the signal peptide and the translation apparatus is detected by the use of a single point mutation which blocks translocation across mammalian endoplasmic reticulum. , 1987, The Journal of biological chemistry.
[14] F. Nagy,et al. Targeting of bacterial chloramphenicol acetyltransferase to mitochondria in transgenic plants , 1987, Nature.
[15] M. Inouye,et al. Wild type and mutant signal peptides of Escherichia coli outer membrane lipoprotein interact with equal efficiency with mammalian signal recognition particle. , 1987, The Journal of biological chemistry.
[16] E. Freire,et al. Thermodynamic characterization of interactions between ornithine transcarbamylase leader peptide and phospholipid bilayer membranes. , 1987, Biochemistry.
[17] T. Rapoport,et al. Protein translocation across wheat germ microsomal membranes requires an SRP‐like component , 1987, The EMBO journal.
[18] G. Müller,et al. Import of honeybee prepromelittin into the endoplasmic reticulum: structural basis for independence of SRP and docking protein. , 1987, The EMBO journal.
[19] R. Lyons,et al. Pentapeptide nuclear localization signal in adenovirus E1a , 1987, Molecular and cellular biology.
[20] S. Miura,et al. A small hydrophobic domain anchors leader peptidase to the cytoplasmic membrane of Escherichia coli. , 1987, The Journal of biological chemistry.
[21] W. Neupert,et al. Mitochondrial protein import: Nucleoside triphosphates are involved in conferring import-competence to precursors , 1987, Cell.
[22] M. Douglas,et al. Phosphodiester bond cleavage outside mitochondria is required for the completion of protein import into the mitochondrial matrix , 1987, Cell.
[23] C. DeLisi,et al. Hydrophobicity scales and computational techniques for detecting amphipathic structures in proteins. , 1987, Journal of molecular biology.
[24] G. Kreibich,et al. The influenza hemagglutinin insertion signal is not cleaved and does not halt translocation when presented to the endoplasmic reticulum membrane as part of a translocating polypeptide , 1987, The Journal of cell biology.
[25] R. E. Webster,et al. Nucleotide sequence of a gene cluster involved in entry of E colicins and single-stranded DNA of infecting filamentous bacteriophages into Escherichia coli , 1987, Journal of bacteriology.
[26] T. Sako,et al. Role of amino-terminal positive charge on signal peptide in staphylokinase export across the cytoplasmic membrane of Escherichia coli. , 1987, The Journal of biological chemistry.
[27] W. DeGrado,et al. Membrane binding and conformational properties of peptides representing the NH2 terminus of influenza HA-2. , 1987, The Journal of biological chemistry.
[28] M. P. Gallagher,et al. Molecular characterization of the oligopeptide permease of Salmonella typhimurium. , 1987, Journal of molecular biology.
[29] T. Stevens,et al. Yeast carboxypeptidase Y can be translocated and glycosylated without its amino-terminal signal sequence , 1987, The Journal of cell biology.
[30] V. Lingappa,et al. Translocation of globin fusion proteins across the endoplasmic reticulum membrane in Xenopus laevis oocytes , 1987, The Journal of cell biology.
[31] K. Walsh,et al. Suppression of a signal sequence mutation by an amino acid substitution in the mature portion of the maltose-binding protein , 1987, Journal of bacteriology.
[32] D. Zakim,et al. The spontaneous incorporation of proteins into preformed bilayers. , 1987, Biochimica et biophysica acta.
[33] W. Neupert,et al. Import of cytochrome c into mitochondria , 1987 .
[34] M. Eilers,et al. Both ATP and an energized inner membrane are required to import a purified precursor protein into mitochondria. , 1987, The EMBO journal.
[35] J. Tommassen,et al. A comparative study on the phoE genes of three enterobacterial species. Implications for structure-function relationships in a pore-forming protein of the outer membrane. , 1987, European journal of biochemistry.
[36] M. Tanner,et al. Human erythrocyte membrane sialoglycoprotein beta. The cDNA sequence suggests the absence of a cleaved N-terminal signal sequence. , 1987, The Biochemical journal.
[37] G. Shore,et al. Import of hybrid vesicular stomatitis G protein to the mitochondrial inner membrane. , 1987, The Journal of biological chemistry.
[38] J. Knowles,et al. The consequences of stepwise deletions from the signal-processing site of beta-lactamase. , 1987, The Journal of biological chemistry.
[39] R. Stroud,et al. Independent mutations at the amino terminus of a protein act as surrogate signals for mitochondrial import. , 1987, The EMBO journal.
[40] R. Lamb,et al. Ability of the hydrophobic fusion-related external domain of a paramyxovirus F protein to act as a membrane anchor , 1987, Cell.
[41] E. Hurt,et al. A cytosolic protein contains a cryptic mitochondrial targeting signal , 1987, Nature.
[42] A. Frey,et al. Determination of the membrane topology of the phenobarbital-inducible rat liver cytochrome P-450 isoenzyme PB-4 using site-specific antibodies , 1987, The Journal of cell biology.
[43] M. Zerial,et al. Foreign transmembrane peptides replacing the internal signal sequence of transferrin receptor allow its translocation and membrane binding , 1987, Cell.
[44] D Botstein,et al. Many random sequences functionally replace the secretion signal sequence of yeast invertase. , 1987, Science.
[45] A. Vassarotti,et al. Sequences distal to the mitochondrial targeting sequences are necessary for the maturation of the F1-ATPase beta-subunit precursor in mitochondria. , 1987, The Journal of biological chemistry.
[46] D. Pilgrim,et al. Primary structure requirements for correct sorting of the yeast mitochondrial protein ADH III to the yeast mitochondrial matrix space , 1987, Molecular and cellular biology.
[47] G. Cesareni,et al. A novel leader peptide which allows efficient secretion of a fragment of human interleukin 1 beta in Saccharomyces cerevisiae. , 1987, The EMBO journal.
[48] F. Opperdoes,et al. Common elements on the surface of glycolytic enzymes from Trypanosoma brucei may serve as topogenic signals for import into glycosomes. , 1987, The EMBO journal.
[49] F. Hartl,et al. Transport into mitochondria and intramitochondrial sorting of the Fe/S protein of ubiquinol-cytochrome c reductase , 1986, Cell.
[50] P. Weisbeek,et al. A thylakoid processing protease is required for complete maturation of the lumen protein plastocyanin , 1986, Nature.
[51] A. Kuhn,et al. Both hydrophobic domains of M13 procoat are required to initiate membrane insertion. , 1986, The EMBO journal.
[52] R. Lamb,et al. Determination of the orientation of an integral membrane protein and sites of glycosylation by oligonucleotide-directed mutagenesis: influenza B virus NB glycoprotein lacks a cleavable signal sequence and has an extracellular NH2-terminal region , 1986, Molecular and cellular biology.
[53] L. Grivell,et al. Targeting efficiency of a mitochondrial pre‐sequence is dependent on the passenger protein. , 1986, The EMBO journal.
[54] Gunnar von Heijne,et al. Net N-C charge imbalance may be important for signal sequence function in bacteria , 1986 .
[55] L. Tamm. Incorporation of a synthetic mitochondrial signal peptide into charged and uncharged phospholipid monolayers. , 1986, Biochemistry.
[56] T. Silhavy,et al. Kinetic analysis of lamB mutants suggests the signal sequence plays multiple roles in protein export. , 1986, The Journal of biological chemistry.
[57] J. Gordon,et al. Deletion of the propeptide from human preproapolipoprotein A-II redirects cotranslational processing by signal peptidase. , 1986, The Journal of biological chemistry.
[58] R A Laskey,et al. Protein import into the cell nucleus. , 1986, Annual review of cell biology.
[59] A. Dunn,et al. Effect of deletions within the leader peptide of pre-ornithine transcarbamylase on mitochondrial import. , 1986, European journal of biochemistry.
[60] G. Heijne. The distribution of positively charged residues in bacterial inner membrane proteins correlates with the trans‐membrane topology , 1986, The EMBO journal.
[61] K. Altendorf,et al. Accessibility of F0 subunits from Escherichia coli ATP synthase. A study with subunit specific antisera. , 1986, European journal of biochemistry.
[62] W. Wickner,et al. The role of the polar, carboxyl-terminal domain of Escherichia coli leader peptidase in its translocation across the plasma membrane. , 1986, The Journal of biological chemistry.
[63] H. Zuber,et al. Structure of light-harvesting antenna complexes of photosynthetic bacteria, cyanobacteria and red algae , 1986 .
[64] F. Jähnig,et al. The structure of melittin in membranes. , 1986, Biophysical journal.
[65] J. Sambrook,et al. Analysis of progressive deletions of the transmembrane and cytoplasmic domains of influenza hemagglutinin , 1986, The Journal of cell biology.
[66] G. Drews,et al. Effect of uncoupler on assembly pathway for pigment-binding protein of bacterial photosynthetic membranes , 1986, Journal of bacteriology.
[67] B. Dobberstein,et al. The membrane-spanning segment of invariant chain (Iγ) contains a potentially cleavable signal sequence , 1986, Cell.
[68] L. Randall,et al. Correlation of competence for export with lack of tertiary structure of the mature species: A study in vivo of maltose-binding protein in E. coli , 1986, Cell.
[69] J. Rochaix,et al. A mitochondrial presequence can transport a chloroplast-encoded protein into yeast mitochondria. , 1986, The Journal of biological chemistry.
[70] C. Arntzen,et al. Evidence for two-step processing of nuclear-encoded chloroplast proteins during membrane assembly , 1986, The Journal of cell biology.
[71] S W Hui,et al. Structural analysis and amphiphilic properties of a chemically synthesized mitochondrial signal peptide. , 1986, The Journal of biological chemistry.
[72] P. Weisbeek,et al. The role of the transit peptide in the routing of precursors toward different chloroplast compartments , 1986, Cell.
[73] Roger D. Kornberg,et al. Synthetic peptides as nuclear localization signals , 1986, Nature.
[74] A. Kuhn,et al. The cytoplasmic carboxy terminus of M13 procoat is required for the membrane insertion of its central domain , 1986, Nature.
[75] F. Jähnig,et al. Models for the structure of outer-membrane proteins of Escherichia coli derived from raman spectroscopy and prediction methods. , 1986, Journal of molecular biology.
[76] S. Munro,et al. An hsp70-like protein in the ER: Identity with the 78 kd glucose-regulated protein and immunoglobulin heavy chain binding protein , 1986, Cell.
[77] M. Eilers,et al. Binding of a specific ligand inhibits import of a purified precursor protein into mitochondria , 1986, Nature.
[78] L. Gierasch,et al. Conformations of signal peptides induced by lipids suggest initial steps in protein export. , 1986, Science.
[79] D Botstein,et al. Secretion-defective mutations in the signal sequence for Saccharomyces cerevisiae invertase , 1986, Molecular and cellular biology.
[80] Susan Clark Bock,et al. Idealization of the hydrophobic segment of the alkaline phosphatase signal peptide , 1986, Nature.
[81] G. Heijne. A new method for predicting signal sequence cleavage sites. , 1986 .
[82] J. Richards,et al. A chemically synthesized pre‐sequence of an imported mitochondrial protein can form an amphiphilic helix and perturb natural and artificial phospholipid bilayers. , 1986, The EMBO journal.
[83] G. Heijne. Mitochondrial targeting sequences may form amphiphilic helices. , 1986 .
[84] J. Rochaix,et al. The cleavable pre‐sequence of an imported chloroplast protein directs attached polypeptides into yeast mitochondria , 1986, EMBO Journal.
[85] P. Borst,et al. How proteins get into microbodies (peroxisomes, glyoxysomes, glycosomes). , 1986, Biochimica et biophysica acta.
[86] G. Heijne. Towards a comparative anatomy of N-terminal topogenic protein sequences , 1986 .
[87] T. Rapoport,et al. The signal sequence of nascent preprolactin interacts with the 54K polypeptide of the signal recognition particle , 1986, Nature.
[88] R M Macnab,et al. Nucleotide sequence of the Escherichia coli motB gene and site-limited incorporation of its product into the cytoplasmic membrane , 1986, Journal of bacteriology.
[89] G. Heijne. Why mitochondria need a genome , 1986 .
[90] B. de Kruijff,et al. Studies on the lipid dependency and mechanism of the translocation of the mitochondrial precursor protein apocytochrome c across model membranes. , 1986, The Journal of biological chemistry.
[91] G. Schatz,et al. The presequences of two imported mitochondrial proteins contain information for intracellular and intramitochondrial sorting , 1986, Cell.
[92] V. Bankaitis,et al. Intragenic reversion mutations that improve export of maltose-binding protein in Escherichia coli malE signal sequence mutants. , 1986, The Journal of biological chemistry.
[93] H. Matsubara,et al. The N‐terminal 21 amino acids of a 70 kDa protein of the yeast mitochondrial outer membrane direct E. coli β‐galactosidase into the mitochondrial matrix space in yeast cells , 1986, FEBS letters.
[94] H. C. Wu,et al. Processing of Bacillus licheniformis penicillinases lacking a lipoprotein modification site in Escherichia coli , 1986, Journal of bacteriology.
[95] A. Horwich,et al. Targeting of pre-ornithine transcarbamylase to mitochondria: Definition of critical regions and residues in the leader peptide , 1986, Cell.
[96] S. Inouye,et al. Effect of amino acid substitutions at the signal peptide cleavage site of the Escherichia coli major outer membrane lipoprotein. , 1986, The Journal of biological chemistry.
[97] L. Guarente,et al. The nine amino-terminal residues of delta-aminolevulinate synthase direct beta-galactosidase into the mitochondrial matrix , 1986, Molecular and cellular biology.
[98] W. Sebald,et al. Nucleotide sequence and transcription of the fbc operon from Rhodopseudomonas sphaeroides. Evaluation of the deduced amino acid sequences of the FeS protein, cytochrome b and cytochrome c1. , 1986, European journal of biochemistry.
[99] S. Emr,et al. The amino terminus of the yeast F1-ATPase beta-subunit precursor functions as a mitochondrial import signal , 1986, The Journal of cell biology.
[100] H. Lodish,et al. An internal signal sequence: The asialoglycoprotein receptor membrane anchor , 1986, Cell.
[101] W. Richardson,et al. Nuclear location signals in polyoma virus large-T , 1986, Cell.
[102] G. Karlin-Neumann,et al. Transit peptides of nuclear‐encoded chloroplast proteins share a common amino acid framework. , 1986, EMBO Journal.
[103] J. Knowles,et al. Signal sequence mutants of beta-lactamase. , 1985, The Journal of biological chemistry.
[104] R. Hodges,et al. A synthetic signal peptide blocks import of precursor proteins destined for the mitochondrial inner membrane or matrix. , 1985, The Journal of biological chemistry.
[105] J. Deisenhofer,et al. Structure of the protein subunits in the photosynthetic reaction centre of Rhodopseudomonas viridis at 3Å resolution , 1985, Nature.
[106] A. Kuhn,et al. Conserved residues of the leader peptide are essential for cleavage by leader peptidase. , 1985, The Journal of biological chemistry.
[107] M. Uhlén,et al. Analysis of signals for secretion in the staphylococcal protein A gene. , 1985, The EMBO journal.
[108] U. Müller,et al. The first twelve amino acids of a yeast mitochondrial outer membrane protein can direct a nuclear‐coded cytochrome oxidase subunit to the mitochondrial inner membrane. , 1985, The EMBO journal.
[109] W. Neupert,et al. Transport of proteins into mitochondria: a potassium diffusion potential is able to drive the import of ADP/ATP carrier. , 1985, The EMBO journal.
[110] D. Oliver,et al. Export defect adjacent to the processing site of staphylococcal nuclease is suppressed by a prlA mutation , 1985, Journal of bacteriology.
[111] Masatoshi Inukai,et al. Dual functions of the signal peptide in protein transfer across the membrane , 1985, Cell.
[112] W. Neupert,et al. Transport of proteins into mitochondria: Translocational intermediates spanning contact sites between outer and inner membranes , 1985, Cell.
[113] H. Lodish,et al. Multiple mechanisms of protein insertion into and across membranes. , 1985, Science.
[114] P. Weisbeek,et al. Sequence of the precursor of the chloroplast thylakoid lumen protein plastocyanin , 1985, Nature.
[115] R. Ellis,et al. Transport of proteins into chloroplasts. The effect of incorporation of amino acid analogues on the import and processing of chloroplast polypeptides. , 1985, European journal of biochemistry.
[116] D. McGeoch,et al. On the predictive recognition of signal peptide sequences. , 1985, Virus research.
[117] S. Inouye,et al. An alternate pathway for the processing of the prolipoprotein signal peptide in Escherichia coli. , 1985, The Journal of biological chemistry.
[118] C. Schmidt,et al. Studies of synthetic peptide analogs of the amphipathic helix. Structure of complexes with dimyristoyl phosphatidylcholine. , 1985, The Journal of biological chemistry.
[119] D. Meyer. Signal recognition particle (SRP) does not mediate a translational arrest of nascent secretory proteins in mammalian cell‐free systems. , 1985, The EMBO journal.
[120] E. Hurt,et al. The first twelve amino acids (less than half of the pre‐sequence) of an imported mitochondrial protein can direct mouse cytosolic dihydrofolate reductase into the yeast mitochondrial matrix. , 1985, The EMBO journal.
[121] G. von Heijne,et al. Signal sequences: The limits of variation , 1985 .
[122] H. Michel,et al. The ‘heavy’ subunit of the photosynthetic reaction centre from Rhodopseudomonas viridis: isolation of the gene, nucleotide and amino acid sequence , 1985, The EMBO journal.
[123] J. Sambrook,et al. SV40 T antigen and the exocytotic pathway. , 1985, The EMBO journal.
[124] P. Model,et al. An artificial anchor domain: hydrophobicity suffices to stop transfer , 1985, Cell.
[125] J. Rosenbusch,et al. Folding patterns of porin and bacteriorhodopsin. , 1985, The EMBO journal.
[126] L. Gierasch,et al. In vivo function and membrane binding properties are correlated for Escherichia coli lamB signal peptides. , 1985, Science.
[127] R. Schekman,et al. Invertase signal and mature sequence substitutions that delay intercompartmental transport of active enzyme , 1985, The Journal of cell biology.
[128] A. Horwich,et al. A leader peptide is sufficient to direct mitochondrial import of a chimeric protein. , 1985, The EMBO journal.
[129] K. Tagawa,et al. Interaction with mitochondrial membranes of a synthetic peptide with a sequence common to extra peptides of mitochondrial precursor proteins. , 1985, Biochemical and biophysical research communications.
[130] A. Pugsley,et al. Export and secretion of proteins by bacteria , 1985 .
[131] W. Wickner,et al. Effects of two sec genes on protein assembly into the plasma membrane of Escherichia coli. , 1985, The Journal of biological chemistry.
[132] J. Boeke,et al. Fine structure of a membrane anchor domain. , 1985, Journal of molecular biology.
[133] G. Cox,et al. Phosphate-specific transport system of Escherichia coli: nucleotide sequence and gene-polypeptide relationships , 1985, Journal of bacteriology.
[134] U. Müller,et al. A 70‐kd protein of the yeast mitochondrial outer membrane is targeted and anchored via its extreme amino terminus. , 1984, The EMBO journal.
[135] E. Hurt,et al. The amino‐terminal region of an imported mitochondrial precursor polypeptide can direct cytoplasmic dihydrofolate reductase into the mitochondrial matrix. , 1984, The EMBO journal.
[136] G. Heijne. Analysis of the distribution of charged residues in the N‐terminal region of signal sequences: implications for protein export in prokaryotic and eukaryotic cells. , 1984, The EMBO journal.
[137] J. Beckwith,et al. The nucleotide sequence of the gene for malF protein, an inner membrane component of the maltose transport system of Escherichia coli. Repeated DNA sequences are found in the malE-malF intercistronic region. , 1984, The Journal of biological chemistry.
[138] H. C. Wu,et al. Modification and processing of Bacillus licheniformis prepenicillinase in Escherichia coli. Fate of mutant penicillinase lacking lipoprotein modification site. , 1984, The Journal of biological chemistry.
[139] L. Grivell,et al. The DNA sequence of the nuclear gene coding for the 17‐kd subunit VI of the yeast ubiquinol‐cytochrome c reductase: a protein with an extremely high content of acidic amino acids. , 1984, The EMBO journal.
[140] V. Bankaitis,et al. Intragenic suppressor mutations that restore export of maltose binding protein with a truncated signal peptide , 1984, Cell.
[141] Gunnar von Heijne,et al. How signal sequences maintain cleavage specificity. , 1984 .
[142] D. Willey,et al. Structure and topology of cytochrome f in pea chloroplast membranes , 1984, Cell.
[143] S. Gasser,et al. How mitochondria import proteins. , 1984, Biochimica et biophysica acta.
[144] E. Kaiser,et al. Amphiphilic secondary structure: design of peptide hormones. , 1984, Science.
[145] S. Inouye,et al. Requirement for signal peptide cleavage of Escherichia coli prolipoprotein. , 1983, Science.
[146] D Perlman,et al. A putative signal peptidase recognition site and sequence in eukaryotic and prokaryotic signal peptides. , 1983, Journal of molecular biology.
[147] S. Inouye,et al. Effects of the complete removal of basic amino acid residues from the signal peptide on secretion of lipoprotein in Escherichia coli. , 1983, The Journal of biological chemistry.
[148] Gunnar von Heijne,et al. Patterns of Amino Acids near Signal‐Sequence Cleavage Sites , 1983 .
[149] M. Simon,et al. Sensory transducers of E. coli are composed of discrete structural and functional domains , 1983, Cell.
[150] S. Inouye,et al. Prolipoprotein signal peptidase of Escherichia coli requires a cysteine residue at the cleavage site. , 1983, The EMBO journal.
[151] R. Doolittle,et al. A simple method for displaying the hydropathic character of a protein. , 1982, Journal of molecular biology.
[152] F. Oesch,et al. Studies on the biosynthesis of microsomal membrane proteins. Site of synthesis and mode of insertion of cytochrome b5, cytochrome b5 reductase, cytochrome P-450 reductase and epoxide hydrolase. , 1982, European journal of biochemistry.
[153] G vonHeijne,et al. Membrane proteins: the amino acid composition of membrane-penetrating segments. , 1981, European journal of biochemistry.
[154] G. Hortin,et al. Miscleavage at the presequence of rat preprolactin synthesized in pituitary cells incubated with a threonine analog , 1981, Cell.
[155] T. Steitz,et al. The spontaneous insertion of proteins into and across membranes: The helical hairpin hypothesis , 1981, Cell.
[156] J. Boeke,et al. Processing of filamentous phage pre-coat protein. Effect of sequence variations near the signal peptidase cleavage site. , 1980, Journal of molecular biology.
[157] E. Davie,et al. Biosynthesis of bovine plasma proteins in a cell-free system. Amino-terminal sequence of preproalbumin. , 1979, European journal of biochemistry.
[158] T. Rapoport,et al. A signal sequence receptor in the endoplasmic reticulum membrane , 1987, Nature.
[159] K. von Figura,et al. Lysosomal enzymes and their receptors. , 1986, Annual review of biochemistry.
[160] T. Rapoport. Protein translocation across and integration into membranes. , 1986, CRC critical reviews in biochemistry.
[161] Y. Fujiki,et al. Biogenesis of peroxisomes. , 1985, Annual review of cell biology.
[162] H. Mihara,et al. Effects of synthetic model peptides resembling the extension peptides of mitochondrial enzyme precursors on import of the precursors into mitochondria. , 1985, Journal of biochemistry.
[163] D. Oliver. Protein secretion in Escherichia coli. , 1985, Annual review of microbiology.
[164] G. Heijne. Chapter 4 Structural and Thermodynamic Aspects of the Transfer of Proteins into and across Membranes , 1985 .
[165] D. Clayton. Transcription of the mammalian mitochondrial genome. , 1984, Annual review of biochemistry.
[166] D. Eisenberg. Three-dimensional structure of membrane and surface proteins. , 1984, Annual review of biochemistry.
[167] M. Inouye,et al. The outer membrane proteins of Gram-negative bacteria: biosynthesis, assembly, and functions. , 1978, Annual review of biochemistry.