Your browser doesn't support javascript.
loading
Calreticulin-Enigmatic Discovery.
Okura, Gillian C; Bharadwaj, Alamelu G; Waisman, David M.
Afiliación
  • Okura GC; Department of Pathology, Dalhousie University, Halifax, NS B3H 1X5, Canada.
  • Bharadwaj AG; Department of Pathology, Dalhousie University, Halifax, NS B3H 1X5, Canada.
  • Waisman DM; Department of Pathology, Dalhousie University, Halifax, NS B3H 1X5, Canada.
Biomolecules ; 14(7)2024 Jul 19.
Article en En | MEDLINE | ID: mdl-39062580
ABSTRACT
Calreticulin (CRT) is an intrinsically disordered multifunctional protein that plays essential roles intra-and extra-cellularly. The Michalak laboratory has proposed that CRT was initially identified in 1974 by the MacLennan laboratory as the high-affinity Ca2+-binding protein (HACBP) of the sarcoplasmic reticulin (SR). This widely accepted belief has been ingrained in the scientific literature but has never been rigorously tested. In our report, we have undertaken a comprehensive reexamination of this assumption by meticulously examining the majority of published studies that present a proteomic analysis of the SR. These analyses have utilized proteomic analysis of purified SR preparations or purified components of the SR, namely the longitudinal tubules and junctional terminal cisternae. These studies have consistently failed to detect the HACBP or CRT in skeletal muscle SR. We propose that the existence of the HACBP has failed the test of reproducibility and should be retired to the annals of antiquity. Therefore, the scientific dogma that the HACBP and CRT are identical proteins is a non sequitur.
Asunto(s)
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Calreticulina Límite: Animals Idioma: En Revista: Biomolecules Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Calreticulina Límite: Animals Idioma: En Revista: Biomolecules Año: 2024 Tipo del documento: Article País de afiliación: Canadá