Smooth muscle and nonmuscle myosin II are regulated by phosphorylation of the 20 kDa regulatory light chain (RLC) located in the neck region. This region contains a single alpha-helical segment of the myosin heavy chain and the RLC and the essential light chain (ELC). There are three vertebrate genes encoding for nonmuscle myosin IIs, termed IIA and IIB. Platelets express only the IIA isoform, whereas brain expressed predominantly the IIB isoform. Most other cells express nearly equal ratios of IIA and IIB where they are differentially localized. Previous work in our lab has revealed that nonmuscle myosin IIA and myosin IIB have differeing enzymatic and motile properties. In order to better understand the basis for this difference, we have engineered myosin IIA and myosin IIB S-1-like fragments for baculoviral expression. We have fully characterized the transient enzyme kinetics of these two molecules in the presence and absence of actin. Both are characterized by generally slow kinetics (compared to other myosin II isoforms), and each are rate-limted by phosphate release in common with all other myosin II isoforms studied to date. Both myosin IIA and IIB are unusual in that actin does not have a great effect on its ADP affinity and vice versa. Myosin IIB is very unusual in that its ADP release from actomyosin is only three times slower than the rate of phosphate release. Simulations show that the duty ratio (fraction of kinetic cycle spent in high actin affinity AM.ADP or AM states) is 0.2. This is an intermediate value between the usual 0.02-0.05 found for all other myosin II isoforms and the value of 0.6-0.8 found for processive myosins such as myosin V or myosin VI. This implies that the function of myosin IIB in cells may be to hold or maintain tension. We have begun to test this hypothesis using optical trapping nanometry. Preliminary characterization of nonmuscle myosin IIC indicates that it is also a very slow myosin in terms of its rate of actin filament sliding and its steady-state actin-activated MgATPase rate.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Intramural Research (Z01)
Project #
1Z01HL001786-25
Application #
6966904
Study Section
(LMC)
Project Start
Project End
Budget Start
Budget End
Support Year
25
Fiscal Year
2004
Total Cost
Indirect Cost
Name
U.S. National Heart Lung and Blood Inst
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Young, Gavin; Hundt, Nikolas; Cole, Daniel et al. (2018) Quantitative mass imaging of single biological macromolecules. Science 360:423-427
Bond, Lisa M; Sellers, James R; McKerracher, Lisa (2015) Rho kinase as a target for cerebral vascular disorders. Future Med Chem 7:1039-53
Heissler, Sarah M; Sellers, James R (2015) Four things to know about myosin light chains as reporters for non-muscle myosin-2 dynamics in live cells. Cytoskeleton (Hoboken) 72:65-70
Billington, Neil; Revill, Derek J; Burgess, Stan A et al. (2014) Flexibility within the heads of muscle myosin-2 molecules. J Mol Biol 426:894-907
Kim, Kye-Young; Kawamoto, Sachiyo; Bao, Jianjun et al. (2008) The B2 alternatively spliced isoform of nonmuscle myosin II-B lacks actin-activated MgATPase activity and in vitro motility. Biochem Biophys Res Commun 369:124-34
Sellers, James R; Knight, Peter J (2007) Folding and regulation in myosins II and V. J Muscle Res Cell Motil 28:363-70
Iwamoto, Hiroyuki; Oiwa, Kazuhiro; Kovacs, Mihaly et al. (2007) Diversity of structural behavior in vertebrate conventional myosins complexed with actin. J Mol Biol 369:249-64
Kovacs, Mihaly; Thirumurugan, Kavitha; Knight, Peter J et al. (2007) Load-dependent mechanism of nonmuscle myosin 2. Proc Natl Acad Sci U S A 104:9994-9
Kim, Kye-Young; Kovacs, Mihaly; Kawamoto, Sachiyo et al. (2005) Disease-associated mutations and alternative splicing alter the enzymatic and motile activity of nonmuscle myosins II-B and II-C. J Biol Chem 280:22769-75
Kovacs, Mihaly; Wang, Fei; Hu, Aihua et al. (2003) Functional divergence of human cytoplasmic myosin II: kinetic characterization of the non-muscle IIA isoform. J Biol Chem 278:38132-40

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