Literature DB >> 3225847

Nature and distribution of sites of temperature-sensitive folding mutations in the gene for the P22 tailspike polypeptide chain.

R Villafane1, J King.   

Abstract

Temperature-sensitive folding (tsf) mutations in gene 9 of bacteriophage P22 interfere with the folding and association of the tailspike polypeptide chain at restrictive temperature. We report here the location and amino acid substitutions for 24 independent tsf mutants. The distribution of these and previously identified mutations is distinctly non-random; all of the 32 unambiguous sites of tsf mutations are located in the central 350 residues of the 666 residue tailspike polypeptide chain. No ts mutation has been found among the N-terminal 140 amino acids, and none among the C-terminal 170 amino acids. Since the physiological defect in these mutants is the destabilization of an early intermediate in the folding pathway, the localization of the mutants suggests that the central region of the chain is critical for formation or stabilization of this early intermediate. The majority of amino acids that served as sites for the tsf mutations were hydrophilic residues. Sixty percent of the replacements of these residues represented charge changes. This probably reflects the selection for mutant sites at the mature protein surface where the substitutions can be best tolerated without interfering with function. None of the sites of tsf mutations were at aromatic residues, and only one proline site was found. Substitutions at these residues may cause lethal folding defects which are not recovered as tsf mutants. The local sequences at tsf sites resemble those reported for turns. Structural studies identify beta-sheet as the dominant secondary structure. These mutations may disrupt the formation of conformational features of beta-sheets which are repeated, such as turns, associations between pairs of strands, or sheet/sheet packing interactions. Such a model accounts for the occurrence of tsf mutations with similar defective phenotypes at multiple positions along the chain.

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Year:  1988        PMID: 3225847     DOI: 10.1016/0022-2836(88)90359-2

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  17 in total

1.  Pressure dissociation studies provide insight into oligomerization competence of temperature-sensitive folding mutants of P22 tailspike.

Authors:  Brian G Lefebvre; Noelle K Comolli; Matthew J Gage; Anne Skaja Robinson
Journal:  Protein Sci       Date:  2004-05-07       Impact factor: 6.725

2.  Buried hydrophobic side-chains essential for the folding of the parallel beta-helix domains of the P22 tailspike.

Authors:  Scott Betts; Cameron Haase-Pettingell; Kristen Cook; Jonathan King
Journal:  Protein Sci       Date:  2004-09       Impact factor: 6.725

Review 3.  Protein folding.

Authors:  T E Creighton
Journal:  Biochem J       Date:  1990-08-15       Impact factor: 3.857

Review 4.  Roles of beta-turns in protein folding: from peptide models to protein engineering.

Authors:  Anna Marie C Marcelino; Lila M Gierasch
Journal:  Biopolymers       Date:  2008-05       Impact factor: 2.505

5.  Intragenic suppressors of folding defects in the P22 tailspike protein.

Authors:  B Fane; J King
Journal:  Genetics       Date:  1991-02       Impact factor: 4.562

6.  Intragenic suppression of a capsid assembly-defective P22 tailspike mutation.

Authors:  P A Maurides; J J Schwarz; P B Berget
Journal:  Genetics       Date:  1990-08       Impact factor: 4.562

7.  Conformation of P22 tailspike folding and aggregation intermediates probed by monoclonal antibodies.

Authors:  M A Speed; T Morshead; D I Wang; J King
Journal:  Protein Sci       Date:  1997-01       Impact factor: 6.725

8.  Phage P22 tailspike protein: removal of head-binding domain unmasks effects of folding mutations on native-state thermal stability.

Authors:  S Miller; B Schuler; R Seckler
Journal:  Protein Sci       Date:  1998-10       Impact factor: 6.725

9.  Identification of four genes involved in the lysogenic pathway of the Salmonella newington bacterial virus epsilon 34.

Authors:  R Villafane; J Black
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

10.  Genomic analysis of bacteriophage epsilon 34 of Salmonella enterica serovar Anatum (15+).

Authors:  Robert Villafane; Milka Zayas; Eddie B Gilcrease; Andrew M Kropinski; Sherwood R Casjens
Journal:  BMC Microbiol       Date:  2008-12-17       Impact factor: 3.605

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