Literature DB >> 23958008

Invited review: Caseins and the casein micelle: their biological functions, structures, and behavior in foods.

C Holt1, J A Carver, H Ecroyd, D C Thorn.   

Abstract

A typical casein micelle contains thousands of casein molecules, most of which form thermodynamically stable complexes with nanoclusters of amorphous calcium phosphate. Like many other unfolded proteins, caseins have an actual or potential tendency to assemble into toxic amyloid fibrils, particularly at the high concentrations found in milk. Fibrils do not form in milk because an alternative aggregation pathway is followed that results in formation of the casein micelle. As a result of forming micelles, nutritious milk can be secreted and stored without causing either pathological calcification or amyloidosis of the mother's mammary tissue. The ability to sequester nanoclusters of amorphous calcium phosphate in a stable complex is not unique to caseins. It has been demonstrated using a number of noncasein secreted phosphoproteins and may be of general physiological importance in preventing calcification of other biofluids and soft tissues. Thus, competent noncasein phosphoproteins have similar patterns of phosphorylation and the same type of flexible, unfolded conformation as caseins. The ability to suppress amyloid fibril formation by forming an alternative amorphous aggregate is also not unique to caseins and underlies the action of molecular chaperones such as the small heat-shock proteins. The open structure of the protein matrix of casein micelles is fragile and easily perturbed by changes in its environment. Perturbations can cause the polypeptide chains to segregate into regions of greater and lesser density. As a result, the reliable determination of the native structure of casein micelles continues to be extremely challenging. The biological functions of caseins, such as their chaperone activity, are determined by their composition and flexible conformation and by how the casein polypeptide chains interact with each other. These same properties determine how caseins behave in the manufacture of many dairy products and how they can be used as functional ingredients in other foods.
Copyright © 2013 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  amyloid fibril; calcium phosphate sequestration; molecular chaperone; unfolded protein

Mesh:

Substances:

Year:  2013        PMID: 23958008     DOI: 10.3168/jds.2013-6831

Source DB:  PubMed          Journal:  J Dairy Sci        ISSN: 0022-0302            Impact factor:   4.034


  39 in total

1.  The functional roles of the unstructured N- and C-terminal regions in αB-crystallin and other mammalian small heat-shock proteins.

Authors:  John A Carver; Aidan B Grosas; Heath Ecroyd; Roy A Quinlan
Journal:  Cell Stress Chaperones       Date:  2017-04-08       Impact factor: 3.667

Review 2.  Extracellular Protein Phosphorylation, the Neglected Side of the Modification.

Authors:  Eva Klement; Katalin F Medzihradszky
Journal:  Mol Cell Proteomics       Date:  2016-11-10       Impact factor: 5.911

3.  Isolation of Endoplasmic Reticulum Fractions from Mammary Epithelial Tissue.

Authors:  Eric Chanat; Annabelle Le Parc; Hichem Lahouassa; Bouabid Badaoui
Journal:  J Mammary Gland Biol Neoplasia       Date:  2016-04-05       Impact factor: 2.673

4.  Efficacy of mouthrinses with bovine milk and milk protein isolates to accumulate casein in the in situ pellicle.

Authors:  A Kensche; S Pötschke; C Hannig; A Dürasch; T Henle; M Hannig
Journal:  Clin Oral Investig       Date:  2020-03-11       Impact factor: 3.573

5.  Effect of Reducing Agent TCEP on Translational Diffusion and Supramolecular Assembly in Aqueous Solutions of α-Casein.

Authors:  Daria L Melnikova; Vladimir D Skirda; Irina V Nesmelova
Journal:  J Phys Chem B       Date:  2019-03-06       Impact factor: 2.991

6.  Milk-derived mammary epithelial cells as non-invasive source to define stage-specific abundance of milk protein and fat synthesis transcripts in native Sahiwal cows and Murrah buffaloes.

Authors:  Ankita Sharma; Umesh K Shandilya; Monika Sodhi; Pradeep Jatav; Ashok Mohanty; Pranay Jain; Preeti Verma; R S Kataria; Parvesh Kumari; Manishi Mukesh
Journal:  3 Biotech       Date:  2019-02-26       Impact factor: 2.406

7.  The Role of Hydroxyl Channel in Defining Selected Physicochemical Peculiarities Exhibited by Hydroxyapatite.

Authors:  Vuk Uskoković
Journal:  RSC Adv       Date:  2015       Impact factor: 3.361

Review 8.  Recent trends in protein and peptide-based biomaterials for advanced drug delivery.

Authors:  Anastasia Varanko; Soumen Saha; Ashutosh Chilkoti
Journal:  Adv Drug Deliv Rev       Date:  2020-08-29       Impact factor: 15.470

9.  A quantitative calcium phosphate nanocluster model of the casein micelle: the average size, size distribution and surface properties.

Authors:  Carl Holt
Journal:  Eur Biophys J       Date:  2021-04-18       Impact factor: 1.733

Review 10.  Are Physicochemical Properties Shaping the Allergenic Potency of Animal Allergens?

Authors:  Joana Costa; Caterina Villa; Kitty Verhoeckx; Tanja Cirkovic-Velickovic; Denise Schrama; Paola Roncada; Pedro M Rodrigues; Cristian Piras; Laura Martín-Pedraza; Linda Monaci; Elena Molina; Gabriel Mazzucchelli; Isabel Mafra; Roberta Lupi; Daniel Lozano-Ojalvo; Colette Larré; Julia Klueber; Eva Gelencser; Cristina Bueno-Diaz; Araceli Diaz-Perales; Sara Benedé; Simona Lucia Bavaro; Annette Kuehn; Karin Hoffmann-Sommergruber; Thomas Holzhauser
Journal:  Clin Rev Allergy Immunol       Date:  2021-01-07       Impact factor: 8.667

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