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Physiological Reviews, Vol. 79, No. 3, July 1999, pp. 661-682
Copyright ©1999 by the American Physiological Society
Department of Biochemistry, University of Tennessee, Memphis, Tennessee
Jurado, Luis A.,
Priya Sethu Chockalingam, and
Harry W. Jarrett.
Apocalmodulin. Physiol. Rev. 79: 661-682, 1999.
Intracellular Ca2+ is normally maintained at
submicromolar levels but increases during many forms of cellular
stimulation. This increased Ca2+ binds to receptor proteins
such as calmodulin (CaM) and alters the cell's metabolism and
physiology. Calcium-CaM binds to target proteins and alters their
function in such a way as to transduce the Ca2+ signal.
Calcium-free or apocalmodulin (ApoCaM) binds to other proteins and
has other specific effects. Apocalmodulin has roles in the cell that
apparently do not require the ability to bind Ca2+ at all,
and these roles appear to be essential for life. Apocalmodulin differs
from Ca2+-CaM in its tertiary structure. It binds target
proteins differently, utilizing different binding motifs such as the IQ
motif and noncontiguous binding sites. Other kinds of binding
potentially await discovery. The ApoCaM-binding proteins are a
diverse group of at least 15 proteins including enzymes,
actin-binding proteins, as well as cytoskeletal and other membrane
proteins, including receptors and ion channels. Much of the cellular
CaM is bound in a Ca2+-independent manner to membrane
structures within the cell, and the proportion bound changes with cell
growth and density, suggesting it may be a storage form. Apocalmodulin
remains tightly bound to other proteins as subunits and probably
hastens the response of these proteins to Ca2+. The overall
picture that emerges is that CaM cycles between its
Ca2+-bound and Ca2+-free states and in each
state binds to different proteins and performs essential functions.
Although much of the research focus has been on the roles of
Ca2+-CaM, the roles of ApoCaM are equally vital but less
well understood.
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