Literature DB >> 1873462

On the relationship between distance information derived from cross-linking and from resonance energy transfer, with specific reference to sites located on myosin heads.

P D Chantler1, T Tao, W F Stafford.   

Abstract

The techniques of fluorescence resonance energy transfer (FRET) and cross-linking can provide complementary information concerning the relative separation of a pair of sites. Cross-linking experiments provide an assessment of the distance of closest approach between a pair of sites. FRET measurements, by contrast, yield information about the average distance between the pair of sites. We have taken advantage of hybrid myosins to understand the relationship between distances obtained for a pair of equivalent sites, one on each myosin head, using both FRET (steady-state and time-decay) and cross-linking techniques. The rigid cross-linker, 4-4'-dimaleimidyl-stilbene-2-2'-disulfonic acid (DMSDS), can efficiently cross-link the two myosin regulatory light-chains, each at residue Cys50 of the Mercenaria regulatory light chain (Chantler, P.D., and S. M. Bower. 1988. J. Biol. Chem. 263:938-944), indicating that these sites can come within 18 +/- 2 A of each other. In a complementary set of experiments, steady-state and time-decay measurements using fluorescence donor/acceptor pairs located at these same sites indicate transfer efficiencies of somewhat less than 20%, suggesting an average separation of greater than 50 A between sites (Chantler, P. D., and T. Tao. 1986. J. Mol. Biol. 192:87-99). Here, we present theoretical calculations which show that efficient cross-linking can be achieved readily in dynamic systems such as the heads of myosin, even though the necessary subpopulation of proximate molecules at any instant may be below the detection limits of time-decay-FRET. Therefore, cross-linking experiments can provide important ancillary information about the extent of motions within a marcomolecular system when used in conjunction with FRET.As a corollary, demonstration of extensive cross-linking does not necessarily indicate a static proximity; the mean separation distance should be ascertained by other methods such as FRET.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1873462      PMCID: PMC1281204          DOI: 10.1016/S0006-3495(91)82339-6

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  18 in total

1.  Statistical interpretation of fluorescence energy transfer measurements in macromolecular systems.

Authors:  Z Hillel; C W Wu
Journal:  Biochemistry       Date:  1976-05-18       Impact factor: 3.162

2.  Negative staining of myosin molecules.

Authors:  M Walker; P Knight; J Trinick
Journal:  J Mol Biol       Date:  1985-08-05       Impact factor: 5.469

3.  Interhead fluorescence energy transfer between probes attached to translationally equivalent sites on the regulatory light chains of scallop myosin.

Authors:  P D Chantler; T Tao
Journal:  J Mol Biol       Date:  1986-11-05       Impact factor: 5.469

4.  Crosslinking of troponin complex with 1,3-difluoro-4,6-dinitrobenzene. Identification of the crosslink formed between troponin C and troponin I in the absence of Ca2+.

Authors:  A B Dobrovol'sky; N B Gusev; P Friedrich
Journal:  Biochim Biophys Acta       Date:  1984-09-11

5.  Introduction of a donor-acceptor pair by a single protein modification. Förster energy transfer distance measurements from trapped 1,N6-ethenoadenosine diphosphate to chromophoric cross-linking reagents on the critical thiols of myosin subfragment.

Authors:  W J Perkins; J Weiel; J Grammer; R G Yount
Journal:  J Biol Chem       Date:  1984-07-25       Impact factor: 5.157

6.  Reaction of 5,5'-dithiobis(2-nitrobenzoic acid) with myosin subfragment one: evidence for formation of a single protein disulfide with trapping of metal nucleotide at the active site.

Authors:  J A Wells; R G Yount
Journal:  Biochemistry       Date:  1980-04-15       Impact factor: 3.162

7.  An investigation of the SH1-SH2 and SH1-ATPase distances in myosin subfragment-1 by resonance energy transfer using nanosecond fluorimetry.

Authors:  H C Cheung; F Gonsoulin; F Garland
Journal:  Biochim Biophys Acta       Date:  1985-11-08

8.  Ca2+ dependence of the distance between Cys-98 of troponin C and Cys-133 of troponin I in the ternary troponin complex. Resonance energy transfer measurements.

Authors:  T Tao; E Gowell; G M Strasburg; J Gergely; P C Leavis
Journal:  Biochemistry       Date:  1989-07-11       Impact factor: 3.162

9.  Cross-linking between translationally equivalent sites on the two heads of myosin. Relationship to energy transfer results between the same pair of sites.

Authors:  P D Chantler; S M Bower
Journal:  J Biol Chem       Date:  1988-01-15       Impact factor: 5.157

10.  Structural relationships of actin, myosin, and tropomyosin revealed by cryo-electron microscopy.

Authors:  R A Milligan; P F Flicker
Journal:  J Cell Biol       Date:  1987-07       Impact factor: 10.539

View more
  7 in total

Review 1.  Invertebrate muscles: thin and thick filament structure; molecular basis of contraction and its regulation, catch and asynchronous muscle.

Authors:  Scott L Hooper; Kevin H Hobbs; Jeffrey B Thuma
Journal:  Prog Neurobiol       Date:  2008-06-20       Impact factor: 11.685

2.  Structural basis of the relaxed state of a Ca2+-regulated myosin filament and its evolutionary implications.

Authors:  John L Woodhead; Fa-Qing Zhao; Roger Craig
Journal:  Proc Natl Acad Sci U S A       Date:  2013-05-06       Impact factor: 11.205

3.  Holding two heads together: stability of the myosin II rod measured by resonance energy transfer between the heads.

Authors:  Tania Chakrabarty; Ming Xiao; Roger Cooke; Paul R Selvin
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-23       Impact factor: 11.205

4.  Disulphide cross-linking of smooth-muscle and non-muscle caldesmon to the C-terminus of actin in reconstituted and native thin filaments.

Authors:  P Graceffa; L P Adam; W Lehman
Journal:  Biochem J       Date:  1993-08-15       Impact factor: 3.857

5.  Localization of Cys133 of rabbit skeletal troponin-I with respect to troponin-C by resonance energy transfer.

Authors:  Y Luo; J L Wu; J Gergely; T Tao
Journal:  Biophys J       Date:  1998-06       Impact factor: 4.033

6.  Cross-linking myosin subfragment 1 Cys-697 and Cys-707 modifies ATP and actin binding site interactions.

Authors:  K Kirshenbaum; S Papp; S Highsmith
Journal:  Biophys J       Date:  1993-09       Impact factor: 4.033

7.  The molecular basis for sarcomere organization in vertebrate skeletal muscle.

Authors:  Zhexin Wang; Michael Grange; Thorsten Wagner; Ay Lin Kho; Mathias Gautel; Stefan Raunser
Journal:  Cell       Date:  2021-03-24       Impact factor: 66.850

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.