Relocation of Cys374 of Actin Induced by Labeling with Fluorescent Dyes
Abstract
Cys374 is an important landmark of actin, because its sulfhydryl group is reactive and can be labeled with various reagents. The atomic coordinates of actin Cys374 have been determined by X-ray crystallography of co-crystals of actin with either profilin or gelsolin. However, the positions of Cys374 in the crystals determined were not consistent with the data obtained through fluorescence resonance energy transfer. Here, we examined its position by means of probabilistic distance geometry using published fluorescence resonance transfer data and found that Cys374 of actin was relocated when Cys374 was labeled with fluorescent dyes that caused steric hindrance. The atomic coordinates of Cys374 after heavy atom labeling have been found to be different from those for the native crystal. This is consistent with our results. Therefore, the position of Cys374 is sensitive to chemical modification that introduces a bulky reagent. This also suggests that the conformation of the C-terminal region of actin could also be sensitive to the environment.
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Cys374 of actin is solvent exposed and can be labeled with the spin label MTSSL.
“Cys374 of actin is solvent exposed and can be labeled with the spin label MTSSL37–41.”
From Multivalent cross-linking of actin filaments and microtubules through the microtubule-associated protein Tau (2017) · cites this paper as [37]
Actin contains five cysteine residues, and C374 incorporates more than 70% of spin labels during spin labeling reactions.
“Although actin contains five cysteine residues, a number of studies has shown that the C-terminal C374, which is in close proximity to actin’s hydrophobic pocket (Fig. 2d), is most solvent exposed (Supplementary Fig. 4a, b) and incorporates more than 70% of spin labels during spin labeling reactions37–41.”
From Multivalent cross-linking of actin filaments and microtubules through the microtubule-associated protein Tau (2017) · cites this paper as [37]
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Cabrales Fontela, Y., Kadavath, H., Biernat, J., Riedel, D., Mandelkow, E., & Zweckstetter, M. (2017) · Nature Communications · doi:10.1038/s41467-017-02230-8 · Cited by 148 · see citing works
- Authors
- Yasunaga, T., & Wakabayashi, T.
- Affiliations
- The University of Tokyo (JP)
- Venue
- Journal of Biochemistry
- Publisher
- Oxford University Press (OUP)
- Published
- 2001-02-01
- Volume
- 129
- Issue
- 2
- Pages
- 201-204
- ISSN
- 0021-924X (ISSN-L)
- OpenAlex
- W2069599112
- Cited by
- 8
- References
- 0
- Citations by year
- 2025: 1 · 2018: 1 · 2017: 2
- FWCI
- 0.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Physical Sciences › Materials Science › Materials Chemistry › Enzyme Structure and Function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- actin, sulfhydryl groups, fluorescent dye labeling, steric hindrance, chemical modification, actin conformation, C-terminal region, fluorescence resonance energy transfer, heavy atom labeling
- MeSH terms
- Actins, Animals, Cattle, Cysteine, Energy Transfer, Fluorescent Dyes, Models, Molecular, Protein Conformation, Rabbits, Spectrometry, Fluorescence, Crystallography, X-Ray, In Vitro Techniques
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