The kinetic behavior of insulin fibrillation is determined by heterogeneous nucleation pathways

被引:102
作者
Librizzi, F
Rischel, C
机构
[1] Univ Palermo, Dipartimento Sci Fis & Astron, I-90123 Palermo, Italy
[2] Niels Bohr Inst, DK-2100 Copenhagen, Denmark
[3] CNR, Ist Nazl Fis Mat, I-00185 Rome, Italy
关键词
insulin; protein aggregation; amyloids; nucleation; Thioflavin T; fluorescence;
D O I
10.1110/ps.051692305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
When subjected to acidic conditions and high temperature, insulin is known to produce fibrils that display the common properties of disease amyloids. Thus, clarifying the mechanisms of insulin fibrillation can help the general understanding of amyloidal aggregation. Insulin fibrillation exhibits a very sharp time dependence, with a pronounced lag phase and subsequent explosive growth of amyloidal aggregates. Here we show that the initial stages of this process can be well described by exponential growth of the fibrillated proteins. This indicates that the process is mainly controlled by a secondary nucleation pathway.
引用
收藏
页码:3129 / 3134
页数:6
相关论文
共 35 条
  • [1] Formation of insulin amyloid fibrils followed by FTIR simultaneously with CD and electron microscopy
    Bouchard, M
    Zurdo, J
    Nettleton, EJ
    Dobson, CM
    Robinson, CV
    [J]. PROTEIN SCIENCE, 2000, 9 (10) : 1960 - 1967
  • [2] Brange J., 1994, STABILITY INSULIN ST
  • [3] Brange J, 2000, PHARM FORMULATION DE, P89
  • [4] CROSS-BETA PROTEIN STRUCTURES .1. INSULIN FIBRILS
    BURKE, MJ
    ROUGVIE, MA
    [J]. BIOCHEMISTRY, 1972, 11 (13) : 2435 - +
  • [5] Prion diseases of humans and animals: Their causes and molecular basis
    Collinge, J
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 : 519 - 550
  • [6] Protein folding and misfolding
    Dobson, CM
    [J]. NATURE, 2003, 426 (6968) : 884 - 890
  • [7] The behaviour of polyamino acids reveals an inverse side chain effect in amyloid structure formation
    Fändrich, M
    Dobson, CM
    [J]. EMBO JOURNAL, 2002, 21 (21) : 5682 - 5690
  • [8] Amyloid fibrils from muscle myoglobin -: Even an ordinary globular protein can assume a rogue guise if conditions are right.
    Fändrich, M
    Fletcher, MA
    Dobson, CM
    [J]. NATURE, 2001, 410 (6825) : 165 - 166
  • [9] Ferrone F, 1999, METHOD ENZYMOL, V309, P256
  • [10] KINETICS OF SICKLE HEMOGLOBIN POLYMERIZATION .2. A DOUBLE NUCLEATION MECHANISM
    FERRONE, FA
    HOFRICHTER, J
    EATON, WA
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1985, 183 (04) : 611 - 631