Displacement of gold marker in immunoelectron microscopy of human respiratory cilia

✍ Scribed by Umeda, Akira; Torikata, Chikao; Takasugi, Tomoaki; Tanaka, Mitsuru; Yamaguchi, Kazuhiro; Kanazawa, Minoru; Yoshida, Toshimichi

• Publisher: John Wiley and Sons
• Year: 1997
• Tongue: English
• Weight: 153 KB
• Volume: 38
• Category: Article
• ISSN: 1059-910X
• DOI: 10.1002/(sici)1097-0029(19970901)38:5<500::aid-jemt6>3.0.co;2-l

✦ Synopsis

Preembedding immunogold electron microscopy was performed to evaluate the position of outer arm dynein heavy chains in normal human respiratory cilia. Anti-dynein antibody (AD2), which is specific for sea urchin sperm flagellar dynein heavy chains, was used as primary antibody. Direct cross-sections of cilia were selected, and the distance between the center of a cilium and the center of a colloidal gold particle attached to the cilium (X) was measured. The distance between the center of a cilium and the farthest edge of an outer dynein arm of the cilium was measured by ordinary electron microscopy (Yo) and by immunoelectron microscopy (Yi). X was significantly longer than Yo and Yi. If it is assumed that the structure of respiratory cilia is dense and that antibodies are located at the outer side of the actual position of the heavy chains, then the average distance difference of approximately 90-120 Å may represent the length of two conjugated antibodies. This length should be kept in mind when performing immunoelectron microscopy. The data suggest that AD2 recognizes the outer arm dynein heavy chains of normal human respiratory cilia.