We used atomic force/lateral force microscopy (AFM/LFM) and the transfer of a lipophylic fluorescent dye (octadecylrhodamine G, R18) to study morphology and fusion of human prostasomes at pH values ranging between 5 and 8. The AFM data revealed that the mean diameter of untreated prostasomal vesicles was about 200 nm but a second prostasome population with a diameter of about 400 nm is also present. This second population increased upon exposing the vesicles to low pH values. The AFM/LFM characterization revealed the smoothness of prostasome surface and showed that the larger vesicles were fused prostasomes, as also indicated by the relief of R18 self-quenching.
Prostasome self-fusion studied by atomic force microscopy
Girasole M;
2003
Abstract
We used atomic force/lateral force microscopy (AFM/LFM) and the transfer of a lipophylic fluorescent dye (octadecylrhodamine G, R18) to study morphology and fusion of human prostasomes at pH values ranging between 5 and 8. The AFM data revealed that the mean diameter of untreated prostasomal vesicles was about 200 nm but a second prostasome population with a diameter of about 400 nm is also present. This second population increased upon exposing the vesicles to low pH values. The AFM/LFM characterization revealed the smoothness of prostasome surface and showed that the larger vesicles were fused prostasomes, as also indicated by the relief of R18 self-quenching.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
