SwePub
Sök i LIBRIS databas

  Extended search

id:"swepub:oai:DiVA.org:lnu-82905"
 

Search: id:"swepub:oai:DiVA.org:lnu-82905" > Comparative analysi...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Comparative analysis of widely used methods to remove nonfunctional myosin heads for the in vitro motility assay

Rahman, Mohammad A. (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB)
Salhotra, Aseem (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Department of Chemistry and Biomedical Sciences, Linnaeus University, Kalmar, Sweden
Månsson, Alf (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB)
 (creator_code:org_t)
2019-03-08
2018
English.
In: Journal of Muscle Research and Cell Motility. - : Springer. - 0142-4319 .- 1573-2657. ; 39:5-6, s. 175-187
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • The in vitro motility assay allows studies of muscle contraction through observation of actin filament propulsion by surface-adsorbed myosin motors or motor fragments isolated from muscle. A possible problem is that motility may be compromised by nonfunctional, "dead", motors, obtained in the isolation process. Here we investigate the effects on motile function of two approaches designed to eliminate the effects of these dead motors. We first tested the removal of heavy meromyosin (HMM) molecules with ATP-insensitive "dead" heads by pelleting them with actin filaments, using ultracentrifugation in the presence of 1 mM MgATP ("affinity purification"). Alternatively we incubated motility assay flow cells, after HMM surface adsorption, with non-fluorescent "blocking actin" (1 µM) to block the dead heads. Both affinity purification and use of blocking actin increased the fraction of motile filaments compared to control conditions. However, affinity purification significantly reduced the actin sliding speed in five out of seven experiments on silanized surfaces and in one out of four experiments on nitrocellulose surfaces. Similar effects on velocity were not observed with the use of blocking actin. However, a reduced speed was also seen (without affinity purification) if HMM or myosin subfragment 1 was mixed with 1 mM MgATP before and during surface adsorption. We conclude that affinity purification can produce unexpected effects that may complicate the interpretation of in vitro motility assays and other experiments with surface adsorbed HMM, e.g. single molecule mechanics experiments. The presence of MgATP during incubation with myosin motor fragments is critical for the complicating effects.

Subject headings

NATURVETENSKAP  -- Biologi -- Cellbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Cell Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biofysik (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biophysics (hsv//eng)

Keyword

Affinity purification
Blocking actin
Cross-bridge cycle
In vitro motility assay
Molecular motor
Myosin
Cell and Organism Biology
Cell- och organismbiologi

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view