Abstract
ABSTRACT We present a streamlined protocol for encapsulating individual Caenorhabditis elegans specimens for thin-section transmission electron microscopy (TEM) using ethylene vinyl alcohol (EVOH) copolymer hollow fibers. These transparent fibers, featuring a 175 μm inner diameter, 25 μm wall thickness, and an approximate molecular weight cutoff of 30 kDa, possess both hydrophilic and hydrophobic properties. This amphiphilic nature helps maintain a potent lumen structure even in dry, open air, enabling precise handling and orientation of small specimens prior to resin polymerization and eliminating the need for remounting. The protocol includes specimen transfer using wire loops, microwave-assisted chemical pre-fixation, dissection on a soft silicone substrate with micro-scissors, and manipulation of hollow fibers using insect pins. This approach preserves the identity of individual specimens throughout processing. During ultramicrotomy, the fiber serves as a visual guide, enhancing alignment and reproducibility of sectioning. As proof of principle, we demonstrate well-preserved ultrastructural features in chemically fixed, microwave- assisted resin-embedded C. elegans specimens. This method offers a robust and reproducible alternative to conventional gelatinous media encapsulation, particularly suited for TEM analysis of scarce or small biological samples.
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ABSTRACT
We present a streamlined protocol for encapsulating individual Caenorhabditis elegans specimens for thin-section transmission electron microscopy (TEM) using ethylene vinyl alcohol (EVOH) copolymer hollow fibers. These transparent fibers, featuring a 175 μm inner diameter, 25 μm wall thickness, and an approximate molecular weight cutoff of 30 kDa, possess both hydrophilic and hydrophobic properties. This amphiphilic nature helps maintain a potent lumen structure even in dry, open air, enabling precise handling and orientation of small specimens prior to resin polymerization and eliminating the need for remounting. The protocol includes specimen transfer using wire loops, microwave-assisted chemical pre-fixation, dissection on a soft silicone substrate with micro-scissors, and manipulation of hollow fibers using insect pins. This approach preserves the identity of individual specimens throughout processing. During ultramicrotomy, the fiber serves as a visual guide, enhancing alignment and reproducibility of sectioning. As proof of principle, we demonstrate well-preserved ultrastructural features in chemically fixed, microwave- assisted resin-embedded C. elegans specimens. This method offers a robust and reproducible alternative to conventional gelatinous media encapsulation, particularly suited for TEM analysis of scarce or small biological samples.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Author affiliations updated, redundant sentence deleted in introduction. fixative/ buffer in Material and Methods revised, Table 1 revised.
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