Cilia were isolated from Tetrahymena pyriformis by an ethanol-calcium method. Addition of adenosine triphosphate to a suspension of intact or digitonin-extracted cilia caused a decrease of about 20 per cent in turbidity. Study of fractionated cilia showed that the presence of two distinct axonemal components, the outer fibers and the 30S dynein (the axonemal ATPase protein), was necessary for this effect on turbidity to occur. The decrease in turbidity is interpreted as a result of a specific interaction of ATP with these protein components causing an effective increase in hydration. The high nucleotide specificity suggests that the change in hydration is closely related to the processes responsible for motility. The outer fibers themselves swell when suspended in media of very low ionic strength. The concentration of salt needed to prevent this swelling (2 mM MgSO4 or 30 mM KCl) is about the same as that needed to keep dynein bound to the fibers. The recombination of purified 30S dynein with the outer fibers can be followed by the rise in turbidity resulting from increased dry mass of the particles.
Skip Nav Destination
Article navigation
1 September 1965
Article|
September 01 1965
AN EFFECT OF ADENOSINE TRIPHOSPHATE ON THE LIGHT SCATTERED BY SUSPENSIONS OF CILIA
I. R. Gibbons
I. R. Gibbons
From The Biological Laboratories, Harvard University, Cambridge, Massachusetts
Search for other works by this author on:
I. R. Gibbons
From The Biological Laboratories, Harvard University, Cambridge, Massachusetts
Received:
December 18 1964
Online ISSN: 1540-8140
Print ISSN: 0021-9525
Copyright © 1965 by The Rockefeller University Press
1965
J Cell Biol (1965) 26 (3): 707–712.
Article history
Received:
December 18 1964
Citation
I. R. Gibbons; AN EFFECT OF ADENOSINE TRIPHOSPHATE ON THE LIGHT SCATTERED BY SUSPENSIONS OF CILIA . J Cell Biol 1 September 1965; 26 (3): 707–712. doi: https://doi.org/10.1083/jcb.26.3.707
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement