In: PLOS Biology
5(3), e59
[PDF, 646kB]
Abstract
The bacteriophage phi29 generates large forces to compact its double-stranded DNA genome into a protein capsid by means of a portal motor complex. Several mechanical models for the generation of these high forces by the motor complex predict coupling of DNA translocation to rotation of the head-tail connector dodecamer. Putative connector rotation is investigated here by combining the methods of single-molecule force spectroscopy with polarization-sensitive single-molecule fluorescence. In our experiment, we observe motor function in several packaging complexes in parallel using video microscopy of bead position in a magnetic trap. At the same time, we follow the orientation of single fluorophores attached to the portal motor connector. From our data, we can exclude connector rotation with greater than 99% probability and therefore answer a long-standing mechanistic question.
Dokumententyp: | Zeitschriftenartikel |
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Publikationsform: | Publisher's Version |
Fakultät: | Chemie und Pharmazie |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 540 Chemie |
URN: | urn:nbn:de:bvb:19-epub-15101-1 |
ISSN: | 1545-7885 |
Bemerkung: | This research was supported in part by grants from the National Institutes of Health (grant GM-071552 to CB and grant DE-03606 to DLA) |
Sprache: | Englisch |
Dokumenten ID: | 15101 |
Datum der Veröffentlichung auf Open Access LMU: | 06. Mai 2013, 12:14 |
Letzte Änderungen: | 04. Nov. 2020, 12:55 |