Regulation of myosin phosphatase by a specific interaction with cGMP-dependent protein kinase Iα

HK Surks, N Mochizuki, Y Kasai, SP Georgescu… - Science, 1999 - science.org
HK Surks, N Mochizuki, Y Kasai, SP Georgescu, KM Tang, M Ito, TM Lincoln…
Science, 1999science.org
Contraction and relaxation of smooth muscle are regulated by myosin light-chain kinase and
myosin phosphatase through phosphorylation and dephosphorylation of myosin light
chains. Cyclic guanosine monophosphate (cGMP)–dependent protein kinase Iα (cGKIα)
mediates physiologic relaxation of vascular smooth muscle in response to nitric oxide and
cGMP. It is shown here that cGKIα is targeted to the smooth muscle cell contractile apparatus
by a leucine zipper interaction with the myosin-binding subunit (MBS) of myosin …
Contraction and relaxation of smooth muscle are regulated by myosin light-chain kinase and myosin phosphatase through phosphorylation and dephosphorylation of myosin light chains. Cyclic guanosine monophosphate (cGMP)–dependent protein kinase Iα (cGKIα) mediates physiologic relaxation of vascular smooth muscle in response to nitric oxide and cGMP. It is shown here that cGKIα is targeted to the smooth muscle cell contractile apparatus by a leucine zipper interaction with the myosin-binding subunit (MBS) of myosin phosphatase. Uncoupling of the cGKIα-MBS interaction prevents cGMP-dependent dephosphorylation of myosin light chain, demonstrating that this interaction is essential to the regulation of vascular smooth muscle cell tone.
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