Abstract

BackgroundImmunogold labeling in combination with transmission electron microscopy analysis is a technique frequently used to correlate high-resolution morphology studies with detailed information regarding localization of specific antigens. Although powerful, the methodology has limitations and it is frequently difficult to acquire a stringent system where unspecific low-affinity interactions are removed prior to analysis.ResultsWe here describe a combinatorial strategy where surface plasmon resonance and immunogold labeling are used followed by a direct analysis of the sensor-chip surface by scanning electron microscopy. Using this approach, we have probed the interaction between amyloid-β fibrils, associated to Alzheimer’s disease, and apolipoprotein E, a well-known ligand frequently found co-deposited to the fibrillar form of Aβ in vivo. The results display a lateral binding of ApoE along the amyloid fibrils and illustrates how the gold-beads represent a good reporter of the binding.ConclusionsThis approach exposes a technique with generic features which enables both a quantitative and a morphological evaluation of a ligand-receptor based system. The methodology mediates an advantage compared to traditional immunogold labeling since all washing steps can be monitored and where a high stringency can be maintained throughout the experiment.

Highlights

  • Immunogold labeling in combination with transmission electron microscopy analysis is a technique frequently used to correlate high-resolution morphology studies with detailed information regarding localization of specific antigens

  • We have studied the interaction between amyloid β peptide (Aβ) fibrils and Apolipoprotein E (ApoE) where we, in addition, demonstrate how the technique of immunogold labeling can be combined to illustrate the binding pattern

  • Amyloid formation of Aβ1–40 monitored by Thioflavin T (ThT) assay and transmission electron microscopy (TEM) Aβ1–40 readily forms fibrils under stagnant solutions in PBS and the relative proportion of fibrillar material can be monitored by using the amyloid-specific probe ThT

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Summary

Introduction

Immunogold labeling in combination with transmission electron microscopy analysis is a technique frequently used to correlate high-resolution morphology studies with detailed information regarding localization of specific antigens. Fibrillar aggregates of the amyloid β peptide (Aβ) are considered as one of the hallmarks of AD and their ultrastructural morphology and properties have been extensively studied. The formation of Aβ amyloid fibrils follows a nucleation-dependent path of aggregation. A few endogenous proteins have been found to interfere with the process of Aβ amyloid formation, including proteins containing a BRICHOS domain [8,9,10], transthyretin (TTR) [11,12,13,14,15], clusterin [16], and ApoE [17,18,19,20]. Identification of the mechanism of binding including a morphological evaluation of the binding pattern is of interest

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