@article{bf5dea8350fa4982ae6bcb5b68adc0f0,
title = "Zero-mode waveguides visualize the first steps during gelsolin-mediated actin filament formation",
abstract = "Actin filament dynamics underlie key cellular processes. Although the elongation of actin filaments has been extensively studied, the mechanism of nucleation remains unclear. The micromolar concentrations needed for filament formation have prevented direct observation of nucleation dynamics on the single molecule level. To overcome this limitation, we have used the attoliter excitation volume of zero-mode waveguides to directly monitor the early steps of filament assembly. Immobilizing single gelsolin molecules as a nucleator at the bottom of the zero-mode waveguide, we could visualize the actin filament nucleation process. The process is surprisingly dynamic, and two distinct populations during gelsolin-mediated nucleation are observed. The two populations are defined by the stability of the actin dimers and determine whether elongation occurs. Furthermore, by using an inhibitor to block flattening, a conformational change in actin associated with filament formation, elongation was prevented. These observations indicate that a conformational transition and pathway competition determine the nucleation of gelsolin-mediated actin filament formation.",
author = "Maria Hoyer and Crevenna, {Alvaro H.} and Correia, {Jose Rafael Cabral} and Quezada, {Andrea G.} and Lamb, {Don C.}",
note = "Funding Information: This work was supported by a grant from the Deutsche Forschungsgemeinschaft through the SPP 1464 (to A.H.C. and D.C.L.), the Excellent Clusters Nanosystems Initative Munich (NIM) and Center for Integrated Protein Science Munich (CIPSM) , and the Ludwig-Maximilians-Universit{\"a}t M{\"u}nchen (via the LMUInnovativ BioImaging Network (BIN) and the Center for NanoScience (CeNS) ). Work in the Crevenna laboratory was financially supported by Project LISBOA-01-0145-FEDER-007660 (Microbiologia Molecular, Estrutural e Celular) funded by FEDER funds through COMPETE2020 - Programa Operacional Competitividade e Internacionaliza{\c c}{\~a}o (POCI) and by national funds through FCT - Funda{\c c}{\~a}o para a Ci{\^e}ncia e a Tecnologia. A.G.Q. was granted a scholarship 2018-000022-01EXTV-00471 from Consejo Nacional de Ciencia y Tecnolog{\'i}a CONACYT . Funding Information: This work was supported by a grant from the Deutsche Forschungsgemeinschaft through the SPP 1464 (to A.H.C. and D.C.L.), the Excellent Clusters Nanosystems Initative Munich (NIM) and Center for Integrated Protein Science Munich (CIPSM), and the Ludwig-Maximilians-Universit?t M?nchen (via the LMUInnovativ BioImaging Network (BIN) and the Center for NanoScience (CeNS)). Work in the Crevenna laboratory was financially supported by Project LISBOA-01-0145-FEDER-007660 (Microbiologia Molecular, Estrutural e Celular) funded by FEDER funds through COMPETE2020 - Programa Operacional Competitividade e Internacionaliza??o (POCI) and by national funds through FCT - Funda??o para a Ci?ncia e a Tecnologia. A.G.Q. was granted a scholarship 2018-000022-01EXTV-00471 from Consejo Nacional de Ciencia y Tecnolog?a CONACYT. Publisher Copyright: {\textcopyright} 2021",
year = "2022",
month = jan,
day = "18",
doi = "10.1016/j.bpj.2021.12.011",
language = "English",
volume = "121",
pages = "327--335",
journal = "Biophysical Journal",
issn = "0006-3495",
publisher = "Biophysical Society | Cell Press | Elsevier",
number = "2",
}