Literature DB >> 3541913

A novel isoform of cytoplasmic actin that binds poly-L-proline.

N L Kedersha, D Broek, R A Berg.   

Abstract

An actin-like protein was purified to apparent homogeneity from chick-embryo homogenates and chick-embryo fibroblasts by the use of poly-L-proline-agarose affinity chromatography; we therefore refer to this protein as PBP (poly-L-proline-binding protein). PBP binds to deoxyribonuclease-agarose, co-migrates with known actin standards on SDS/polyacrylamide-gel electrophoresis, and has an amino acid composition similar to that of actin. Linear peptide maps after digestion with Staphylococcus aureus proteinase reveal its apparent homology with gamma-actin; however, isoelectric-focusing experiments show that PBP is clearly more acidic than any of the three major isoforms of actin. PBP polymerizes in the presence of ATP to form fibrillar structures resembling actin paracrystalline aggregates. In chick-embryo fibroblasts, immunofluorescence with antibodies to PBP shows that its distribution is cytoplasmic: perinuclear staining of the cytoplasm, generalized cytoplasmic staining and peripheral fibrillar structures are evident. In contrast, antibodies specific for the (alpha, gamma)-actins reveal the typical stress fibre structures characteristic of fibroblastic cells. PBP appears to constitute a novel isoform of cellular actin, distinct from the known actin isoforms in terms of its lower isoelectric point, its ability to bind poly-L-proline and its distinct subcellular localization.

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Year:  1986        PMID: 3541913      PMCID: PMC1147170          DOI: 10.1042/bj2380561

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  35 in total

1.  Non-identity of muscle and non-muscle actins.

Authors:  E Gruenstein; A Rich
Journal:  Biochem Biophys Res Commun       Date:  1975-05-19       Impact factor: 3.575

2.  A second form of actin: platelet microfilaments depolymerized by ATP and divalent cations.

Authors:  J W Abramowitz; A Stracher; T C Detwiler
Journal:  Arch Biochem Biophys       Date:  1975-03       Impact factor: 4.013

3.  ACTIN: A COMPARATIVE STUDY.

Authors:  M E CARSTEN; A M KATZ
Journal:  Biochim Biophys Acta       Date:  1964-09-04

4.  High resolution two-dimensional electrophoresis of proteins.

Authors:  P H O'Farrell
Journal:  J Biol Chem       Date:  1975-05-25       Impact factor: 5.157

5.  Affinity column purification of protocollagen proline hydroxylase from chick embryos and further characterization of the enzyme.

Authors:  R A Berg; D J Prockop
Journal:  J Biol Chem       Date:  1973-02-25       Impact factor: 5.157

6.  Purification from crude extract by affinity chromatography of the inhibitor of deoxyribonucleae I.

Authors:  U Lindberg; S Eriksson
Journal:  Eur J Biochem       Date:  1971-02

7.  An affinity-column procedure using poly(L-proline) for the purification of prolyl hydroxylase. Purification of the enzyme from chick embryos.

Authors:  L Tuderman; E R Kuutti; K I Kivirikko
Journal:  Eur J Biochem       Date:  1975-03-03

8.  Human heart and platelet actins are products of different genes.

Authors:  M Elzinga; B J Maron; R S Adelstein
Journal:  Science       Date:  1976-01-09       Impact factor: 47.728

9.  Actin is the naturally occurring inhibitor of deoxyribonuclease I.

Authors:  E Lazarides; U Lindberg
Journal:  Proc Natl Acad Sci U S A       Date:  1974-12       Impact factor: 11.205

10.  Actin associated with membranes from 3T3 mouse fibroblast and HeLa cells.

Authors:  E Gruenstein; A Rich; R R Weihing
Journal:  J Cell Biol       Date:  1975-01       Impact factor: 10.539

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  1 in total

1.  A simple procedure for the isolation of protein disulphide-isomerase.

Authors:  J Koivu; R Myllylä; K I Kivirikko
Journal:  Biochem J       Date:  1987-10-01       Impact factor: 3.857

  1 in total

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