Real-time analysis and direct observations of different superoxide dismutase (SOD1) molecules bindings to aggregates in temporal evolution step

  • Hong, Surin
  • Lee, Suseung
  • Choi, Inhee
  • Yang, Young In
  • Kang, Taewook
  • 외 1명
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초록

The misfolding and intracellular aggregation of Cu-Zn superoxide dismutase (SOD1) is pathologically key feature of amyotrophic lateral sclerosis (AIS). Although details of the mechanisms continue to be unclear, there are key steps in the possible pathway to the development of ALS. This study focuses on interactions between different SOD1 molecules (A4V apo/holo, and WT apo/holo) and homogeneous aggregates in the temporal evolution step, and a determination of whether any of the SOD1 molecules are reactive to the aggregates with the extent of binding, as determined by surface plasmon resonance (SPR) measurements. Using a kinetic binding model, the association constant of A4V apo was found to be three times larger than that for the WT apo species. Differences in the extent of the interactions were also simultaneously measured and visualized by means of SPR imaging techniques. The SPR-based approach suggests direct correlation between SPR signal and the extent of molecular binding, which can identify the significant contributors to the formation of macroaggregates of SOD1 in the temporal evolution step. (C) 2012 Elsevier B.V. All rights reserved.

키워드

Binding kineticsSurface plasmon resonance (SPR)SPR imagingProtein aggregationReal-time analysisSuperoxide dismutase1 (SOD1)AMYOTROPHIC-LATERAL-SCLEROSISSURFACE-PLASMON RESONANCEASSEMBLED MONOLAYERSSTABILITYALSDISAGGREGATIONIMMUNOSENSORINTERMEDIATESPECTROSCOPYMUTATIONS
제목
Real-time analysis and direct observations of different superoxide dismutase (SOD1) molecules bindings to aggregates in temporal evolution step
저자
Hong, SurinLee, SuseungChoi, InheeYang, Young InKang, TaewookYi, Jongheop
DOI
10.1016/j.colsurfb.2012.06.014
발행일
2013-01-01
유형
Article
저널명
Colloids and Surfaces B: Biointerfaces
101
페이지
266 ~ 271