Literature DB >> 3518425

Computer prediction of peptide maps: assignment of polypeptides to human and mouse mitochondrial DNA genes by analysis of two-dimensional-proteolytic digest gels.

D C Wallace, J H Yang, J H Ye, M T Lott, N A Oliver, J McCarthy.   

Abstract

We have prepared a computer program that predicts complete and partial peptide maps from amino acid sequences. The program fragments amino acid sequences at designated cleavage sites and calculates the molecular weight and relative labeling of each peptide. These data are graphed as log molecular weight of the original protein (X-axis) vs. log molecular weight of the component peptides (Y-axis). The program is interactive, permitting adjustment of a number of graphic parameters and alteration of the position of proteins in the first dimension to accommodate aberrations in protein mobility. The program has been used to predict the V8 protease peptide maps of the 13 open reading frames (ORFs) identified in the human and the mouse mitochondrial DNA (mtDNA) sequences. The results were compared to the V8 protease peptide maps obtained for mouse and human mitochondrially synthesized proteins by two-dimensional proteolytic digest gels. A high correlation was observed between the predicted and observed peptide maps. These results suggest the assignment of several proteins to mtDNA genes.

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Year:  1986        PMID: 3518425      PMCID: PMC1684801     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  30 in total

1.  Electrophoretic behavior of cytochrome b in a partially purified preparation and evidence for high molecular weight associated mitochondrial translation products.

Authors:  D S Beattie; Y S Chen; L Clejan; L F Lin
Journal:  Biochemistry       Date:  1979-05-29       Impact factor: 3.162

2.  Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis.

Authors:  D W Cleveland; S G Fischer; M W Kirschner; U K Laemmli
Journal:  J Biol Chem       Date:  1977-02-10       Impact factor: 5.157

3.  Sequence homology analysis of a heterogenous protein population by chemical and enzymic digestion using a two-dimensional sodium dodecyl sulfate-polyacrylamide gel system.

Authors:  K S Lam; C B Kasper
Journal:  Anal Biochem       Date:  1980-11-01       Impact factor: 3.365

4.  Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs.

Authors:  J Montoya; D Ojala; G Attardi
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

5.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

6.  Staphylococcal protease: a proteolytic enzyme specific for glutamoyl bonds.

Authors:  J Houmard; G R Drapeau
Journal:  Proc Natl Acad Sci U S A       Date:  1972-12       Impact factor: 11.205

7.  Cyclosporin A promotes spontaneous outgrowth in vitro of Epstein-Barr virus-induced B-cell lines.

Authors:  A G Bird; S M McLachlan; S Britton
Journal:  Nature       Date:  1981-01-22       Impact factor: 49.962

8.  Maternal inheritance of human mitochondrial DNA.

Authors:  R E Giles; H Blanc; H M Cann; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

9.  Isolation, subunit composition, and site of synthesis of human cytochrome c oxidase.

Authors:  J F Hare; E Ching; G Attardi
Journal:  Biochemistry       Date:  1980-05-13       Impact factor: 3.162

10.  Peptide mapping of heterogeneous protein samples.

Authors:  C Bordier; A Crettol-Järvinen
Journal:  J Biol Chem       Date:  1979-04-25       Impact factor: 5.157

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  10 in total

Review 1.  Diseases resulting from mitochondrial DNA point mutations.

Authors:  D C Wallace; M T Lott; J M Shoffner; M D Brown
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

Authors:  M D Brown; A S Voljavec; M T Lott; A Torroni; C C Yang; D C Wallace
Journal:  Genetics       Date:  1992-01       Impact factor: 4.562

3.  Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

Authors:  M Zeviani; P Amati; N Bresolin; C Antozzi; G Piccolo; A Toscano; S DiDonato
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

4.  Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.

Authors:  A S Jun; I A Trounce; M D Brown; J M Shoffner; D C Wallace
Journal:  Mol Cell Biol       Date:  1996-03       Impact factor: 4.272

5.  Copper-dependent inhibition of human cytochrome c oxidase by a dimeric conformer of amyloid-beta1-42.

Authors:  Peter J Crouch; Rachel Blake; James A Duce; Giuseppe D Ciccotosto; Qiao-Xin Li; Kevin J Barnham; Cyril C Curtain; Robert A Cherny; Roberto Cappai; Thomas Dyrks; Colin L Masters; Ian A Trounce
Journal:  J Neurosci       Date:  2005-01-19       Impact factor: 6.167

Review 6.  Molecular basis of mitochondrial DNA disease.

Authors:  M D Brown; D C Wallace
Journal:  J Bioenerg Biomembr       Date:  1994-06       Impact factor: 2.945

7.  Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases.

Authors:  J Lauber; C Marsac; B Kadenbach; P Seibel
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

Review 8.  Mitochondrial DNA sequence variation in human evolution and disease.

Authors:  D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

9.  A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.

Authors:  M D Brown; C C Yang; I Trounce; A Torroni; M T Lott; D C Wallace
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

10.  Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

Authors:  I Trounce; S Neill; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-30       Impact factor: 11.205

  10 in total

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