Literature DB >> 27587511

Common fixation-permeabilization methods cause artifactual localization of a type II transmembrane protein.

Ron Benyair1, Gerardo Z Lederkremer2.   

Abstract

We found that a localization artifact can arise from common immunofluorescence methods. Specifically, cell fixation and permeabilization can cause mislocalization of a type II membrane-bound protein, ER mannosidase I, from its native localization in vesicles to the Golgi complex. Live cell microscopy and interestingly also mild cell fixation with paraformaldehyde without membrane permeabilization do not present this artifact.
© The Author 2016. Published by Oxford University Press on behalf of The Japanese Society of Microscopy. All rights reserved.For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Golgi; fixation; mannosidase; permeabilization; transmembrane protein; vesicles

Mesh:

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Year:  2016        PMID: 27587511     DOI: 10.1093/jmicro/dfw035

Source DB:  PubMed          Journal:  Microscopy (Oxf)        ISSN: 2050-5698            Impact factor:   1.571


  2 in total

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Authors:  Julie Gaston; Nicolas Maestrali; Guilhem Lalle; Marie Gagnaire; Alessandro Masiero; Bruno Dumas; Tarik Dabdoubi; Katarina Radošević; Pierre-François Berne
Journal:  Sci Rep       Date:  2019-12-10       Impact factor: 4.379

2.  Translocation of chromatin proteins to nucleoli-The influence of protein dynamics on post-fixation localization.

Authors:  Mirosław Zarębski; Rosevalentine Bosire; Julita Wesołowska; Oskar Szelest; Ahmed Eatmann; Katarzyna Jasińska-Konior; Oliver Kepp; Guido Kroemer; Gabor Szabo; Jurek W Dobrucki
Journal:  Cytometry A       Date:  2021-06-10       Impact factor: 4.714

  2 in total

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