Literature DB >> 30861328

Using the SpyTag SpyCatcher system to label smooth muscle myosin II filaments with a quantum dot on the regulatory light chain.

Richard K Brizendine1, Murali Anuganti1, Christine R Cremo1.   

Abstract

The regulatory light chain (RLC) of myosin is commonly tagged to monitor myosin behavior in vitro, in muscle fibers, and in cells. The goal of this study was to prepare smooth muscle myosin (SMM) filaments containing a single head labeled with a quantum dot (QD) on the RLC. We show that when the RLC is coupled to a QD at Cys-108 and exchanged into SMM, subsequent filament assembly is severely disrupted. To address this, we used a novel approach for myosin by implementing the SpyTag002 SpyCatcher002 system to prepare SMM incorporated with RLC constructs fused to SpyTag or SpyCatcher. We show that filament assembly, actin-activated steady-state ATPase activities, ability to be phosphorylated, and selected enzymatic and mechanical properties were essentially unaffected if either SpyTag or SpyCatcher were fused to the C-terminus of the RLC. Crucially for our application, we also show that a QD coupled to SpyCatcher can be covalently attached to a RLC-Spy incorporated into a SMM filament without disrupting the filament, and that the filaments can move along actin in vitro.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  electron microscopy; myosin filaments; quantum dots; regulatory light chain; total internal reflection microscopy

Mesh:

Substances:

Year:  2019        PMID: 30861328      PMCID: PMC6520152          DOI: 10.1002/cm.21516

Source DB:  PubMed          Journal:  Cytoskeleton (Hoboken)        ISSN: 1949-3592


  37 in total

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Journal:  Science       Date:  2005-01-28       Impact factor: 47.728

2.  The N-terminal lobes of both regulatory light chains interact with the tail domain in the 10 S-inhibited conformation of smooth muscle myosin.

Authors:  Bridget Salzameda; Kevin C Facemyer; Brian W Beck; Christine R Cremo
Journal:  J Biol Chem       Date:  2006-09-29       Impact factor: 5.157

3.  Charge replacement near the phosphorylatable serine of the myosin regulatory light chain mimics aspects of phosphorylation.

Authors:  H L Sweeney; Z Yang; G Zhi; J T Stull; K M Trybus
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-15       Impact factor: 11.205

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Authors:  T S Allen; N Ling; M Irving; Y E Goldman
Journal:  Biophys J       Date:  1996-04       Impact factor: 4.033

5.  Phosphorylation regulates the ADP-induced rotation of the light chain domain of smooth muscle myosin.

Authors:  J Gollub; C R Cremo; R Cooke
Journal:  Biochemistry       Date:  1999-08-03       Impact factor: 3.162

6.  The kinetics underlying the velocity of smooth muscle myosin filament sliding on actin filaments in vitro.

Authors:  Brian D Haldeman; Richard K Brizendine; Kevin C Facemyer; Josh E Baker; Christine R Cremo
Journal:  J Biol Chem       Date:  2014-07-25       Impact factor: 5.157

7.  Phosphorylation-dependent structural changes in the regulatory light chain domain of smooth muscle heavy meromyosin.

Authors:  X Wu; B A Clack; G Zhi; J T Stull; C R Cremo
Journal:  J Biol Chem       Date:  1999-07-16       Impact factor: 5.157

8.  A new method to specifically label thiophosphorylatable proteins with extrinsic probes. Labeling of serine-19 of the regulatory light chain of smooth muscle myosin.

Authors:  K C Facemyer; C R Cremo
Journal:  Bioconjug Chem       Date:  1992 Sep-Oct       Impact factor: 4.774

9.  Myosin essential light chain isoforms modulate the velocity of shortening propelled by nonphosphorylated cross-bridges.

Authors:  J D Matthew; A S Khromov; K M Trybus; A P Somlyo; A V Somlyo
Journal:  J Biol Chem       Date:  1998-11-20       Impact factor: 5.157

10.  The C-terminal helix in subdomain 4 of the regulatory light chain is essential for myosin regulation.

Authors:  T Rowe; J Kendrick-Jones
Journal:  EMBO J       Date:  1993-12       Impact factor: 11.598

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  1 in total

1.  Evidence for S2 flexibility by direct visualization of quantum dot-labeled myosin heads and rods within smooth muscle myosin filaments moving on actin in vitro.

Authors:  Richard K Brizendine; Murali Anuganti; Christine R Cremo
Journal:  J Gen Physiol       Date:  2021-03-01       Impact factor: 4.086

  1 in total

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