Engineering amyloid and amyloid-like morphologies of β-lactoglobulin

被引:29
作者
Hoppenreijs, L. J. G. [1 ]
Fitzner, L. [2 ]
Ruhmlieb, T. [2 ]
Heyn, T. R. [2 ]
Schild, K. [1 ,2 ]
van der Goot, A-J [1 ]
Boom, R. M. [1 ]
Steffen-Heins, A. [2 ]
Schwarz, K. [2 ]
Keppler, J. K. [1 ,2 ]
机构
[1] Wageningen Univ & Res, Lab Food Proc Engn, Bornse Weilanden 9, NL-6708 WG Wageningen, Netherlands
[2] Univ Kiel, Div Food Technol, Heinrich Hecht Pl 10, D-24118 Kiel, Germany
关键词
Aggregation; Flexibility; Fibrils; Worm-like aggregates; Peptides; Network; WHEY-PROTEIN FIBRIL; BUILDING-BLOCKS; AGGREGATION; HEAT; SHEAR; PEPTIDE; POLYMORPHISM; NANOFIBRILS; STABILITY; KINETICS;
D O I
10.1016/j.foodhyd.2021.107301
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Background: Depending on environmental conditions, almost all proteins can form amyloid and amyloid-like aggregates that have unique functional properties. This opens numerous applications for designed aggregates in materials, medical and food applications. However, it is poorly understood how the amyloid (-like) aggregation and their resulting morphology is induced or influenced by various environmental and processing conditions. Scope and approach: We identified and summarized conditions under which amyloid (-like) aggregates are formed and their impact on aggregate morphology. The focus is on beta-lactoglobulin, but generic effects on other proteins are discussed, in order to elucidate common mechanistic properties. Key findings and conclusions: The flexibility of linear aggregates can be evaluated by comparing the persistence (L-p) and contour length (i.e., length when completely stretched; L-c). Shorter and more flexible amyloid-like aggregates (L-p < L-c) usually occur from a relatively fast assembly (e.g., low repulsion, high concentration, solvents). Longer, semi-flexible amyloid aggregates (L-p similar to L-c) based on fibrillization-prone peptides that are slowly formed and assembled (e.g., high repulsion, low concentration). In either case, the aggregation kinetics increases through protein destabilization (e.g., heating, zinc addition, solvent and hydrolysis effects) and decreases through stabilization (e.g., glycerol addition). Post-processing (e.g., mechanical or interfacial stress) fragments aggregates into stiffer rods (L-p > L-c). Semi-flexible morphologies can align in liquid crystalline phases or interact with linear polysaccharides; while flexible aggregates can entangle. This allows for various possibilities to build higher order fibril or hybrid networks for various applications, such as bundles, coatings/films, or gels. This knowledge is crucial to produce specific morphologies for applications and to draw conclusions about how morphologies will be affected during processing (e.g., shearing).
引用
收藏
页数:15
相关论文
共 125 条
  • [1] Amyloid Polymorphism in the Protein Folding and Aggregation Energy Landscape
    Adamcik, Jozef
    Mezzenga, Raffaele
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (28) : 8370 - 8382
  • [2] Adjustable twisting periodic pitch of amyloid fibrils
    Adamcik, Jozef
    Mezzenga, Raffaele
    [J]. SOFT MATTER, 2011, 7 (11) : 5437 - 5443
  • [3] Micrometer-sized fibrillar protein aggregates from soy glycinin and soy protein isolate
    Akkermans, C.
    Van Der Goot, A. J.
    Venema, P.
    Gruppen, H.
    Vereijken, J. M.
    Van Der Linden, E.
    Boom, R. M.
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (24) : 9877 - 9882
  • [4] Akkermans C., 2008, Protein fibrillization: preparation, mechanism and application
  • [5] Enzyme-Induced Formation of β-Lactoglobulin Fibrils by AspN Endoproteinase
    Akkermans, Cynthia
    Venema, Paul
    van der Goot, Atze Jan
    Boom, Remko M.
    van der Linden, Erik
    [J]. FOOD BIOPHYSICS, 2008, 3 (04) : 390 - 394
  • [6] Formation of fibrillar whey protein aggregates: Influence of heat and shear treatment, and resulting rheology
    Akkermans, Cynthia
    van der Goot, Atze Jan
    Venema, Paul
    van der Linden, Erik
    Boom, Remko M.
    [J]. FOOD HYDROCOLLOIDS, 2008, 22 (07) : 1315 - 1325
  • [7] Peptides are building blocks of heat-induced fibrillar protein aggregates of β-lactoglobulin formed at pH 2
    Akkermans, Cynthia
    Venema, Paul
    van der Goot, Atze Jan
    Gruppen, Harry
    Bakx, Edwin J.
    Boom, Remko M.
    van der Linden, Erik
    [J]. BIOMACROMOLECULES, 2008, 9 (05) : 1474 - 1479
  • [8] Shear pulses nucleate fibril aggregation
    Akkermans, Cynthia
    Venema, Paul
    Rogers, Salman S.
    van der Goot, Atze Jan
    Boom, Remko M.
    van der Linden, Erik
    [J]. FOOD BIOPHYSICS, 2006, 1 (03) : 144 - 150
  • [9] A quercetin-based flavanoid (rutin) reverses amyloid fibrillation in β-lactoglobulin at pH 2.0 and 358 K
    Al-Shabib, Nasser Abdulatif
    Khan, Javed Masood
    Malik, Ajamaluddin
    Sen, Priyankar
    Alsenaidy, Mohammad A.
    Husain, Fohad Mabood
    Alsenaidy, Abdulrahman M.
    Khan, Rizwan Hasan
    Choudhry, Hani
    Zamzami, Mazin A.
    Khan, Mohmmad Imran
    Shahzad, Syed Ali
    [J]. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2019, 214 : 40 - 48
  • [10] Negatively charged food additive dye "Allura Red" rapidly induces SDS-soluble amyloid fibril in beta-lactoglobulin protein
    Al-Shabib, Nasser Abdulatif
    Khan, Javed Masood
    Malik, Ajamaluddin
    Alsenaidy, Abdulrahman M.
    Alsenaidy, Mohammad A.
    Husain, Fohad Mabood
    Shamsi, Monis Bilal
    Hidayathulla, Syed
    Khan, Rizwan Hasan
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 107 : 1706 - 1716