Carrington, G. and Peckham, M. orcid.org/0000-0002-3754-2028 (Accepted: 2026) Why labelling the ‘fast reacting thiols’ of myosin reduces force output: re-assessing a year at the University of California San Francisco. (1987-8). Biophysical Reviews. ISSN: 1867-2450 (In Press)
Abstract
The fast-reacting thiol in the SH1 helix of myosin was often used to attach spin or fluorescent probes to the motor domain, to readout myosin orientation during the 1980s. However, at this time, we found that labelling this residue (Cys707) in myosin in skinned rabbit psoas fibres, using iodoacetacetamidotetramethyl rhodamine (IATR), reduced force output during active contraction. With access to recent pre- and post-powerstroke actomyosin structures, we can now explain these results. We modelled IATR onto the equivalent SH1 cysteine residue in the pre-power and post-power structures of myosin 5. This revealed that labelling of the fast reacting thiol would interfere with the structural changes in the relay and SH1 helices required to generate the power stroke, explaining why force output reduces.
Metadata
| Item Type: | Article |
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| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | This is an author produced version of an article accepted for publication in Biophysical Reviews, made available via the University of Leeds Research Outputs Policy under the terms of the Creative Commons Attribution License (CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
| Keywords: | Myosin, IATR, muscle contraction, fluorescence polarisation |
| Dates: |
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| Institution: | The University of Leeds |
| Academic Units: | The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds) |
| Funding Information: | Funder Grant number Wellcome Trust 223125/Z/21/Z |
| Date Deposited: | 25 Feb 2026 12:59 |
| Last Modified: | 25 Feb 2026 17:38 |
| Status: | In Press |
| Publisher: | Springer |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:238305 |

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