Literature DB >> 4052414

Labelling of erythrocyte spectrin in situ with phenylisothiocyanate.

A F Sikorski, M Kuczek.   

Abstract

The labelling of erythrocyte spectrin in situ with the hydrophobic reagent phenylisothiocyanate (Sigrist, H. and Zahler, P. (1978) FEBS Lett. 95, 116-120) is studied. Spectrin isolated from erythrocytes which have been incubated with phenylisothiocyanate is covalently modified by the probe. The modification in the spectrin molecule is stable under an excess of nucleophile in alkaline conditions. The labelling is very little or not affected by preincubation of erythrocytes of membranes with the polar, structural analogue of phenylisothiocyanate, p-sulfophenylisothiocyanate. When erythrocyte ghosts are subjected to labelling, a substantial increase in the degree of spectrin modification is observed. Subunits of labelled spectrin separated electrophoretically show similar amounts of attached label.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 4052414     DOI: 10.1016/0005-2736(85)90226-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  5 in total

Review 1.  Actin binding proteins--lipid interactions.

Authors:  G Isenberg
Journal:  J Muscle Res Cell Motil       Date:  1991-04       Impact factor: 2.698

2.  Brain spectrin (fodrin) interacts with phospholipids as revealed by intrinsic fluorescence quenching and monolayer experiments.

Authors:  W Diakowski; A Prychidny; M Swistak; M Nietubyć; K Białkowska; J Szopa; A F Sikorski
Journal:  Biochem J       Date:  1999-02-15       Impact factor: 3.857

Review 3.  Interaction of the cytoskeleton with the plasma membrane.

Authors:  V Niggli; M M Burger
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

4.  3-(Trifluoromethyl)-3-(m-isothiocyanophenyl)diazirine: synthesis and chemical characterization of a heterobifunctional carbene-generating crosslinking reagent.

Authors:  M Dolder; H Michel; H Sigrist
Journal:  J Protein Chem       Date:  1990-08

5.  Neural cell adhesion molecule promotes accumulation of TGN organelles at sites of neuron-to-neuron contacts.

Authors:  Vladimir Sytnyk; Iryna Leshchyns'ka; Markus Delling; Galina Dityateva; Alexander Dityatev; Melitta Schachner
Journal:  J Cell Biol       Date:  2002-11-18       Impact factor: 10.539

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.