A modeling approach to the self-assembly of the Golgi apparatus

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A modeling approach to the self-assembly of the Golgi apparatus. / Kühnle, Jens; Shillcock, Julian; Mouritsen, Ole G.; Weiss, Matthias.

In: Biophysical Journal, Vol. 98, No. 12, 16.06.2010, p. 2839-2847.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Kühnle, J, Shillcock, J, Mouritsen, OG & Weiss, M 2010, 'A modeling approach to the self-assembly of the Golgi apparatus', Biophysical Journal, vol. 98, no. 12, pp. 2839-2847. https://doi.org/10.1016/j.bpj.2010.03.035

APA

Kühnle, J., Shillcock, J., Mouritsen, O. G., & Weiss, M. (2010). A modeling approach to the self-assembly of the Golgi apparatus. Biophysical Journal, 98(12), 2839-2847. https://doi.org/10.1016/j.bpj.2010.03.035

Vancouver

Kühnle J, Shillcock J, Mouritsen OG, Weiss M. A modeling approach to the self-assembly of the Golgi apparatus. Biophysical Journal. 2010 Jun 16;98(12):2839-2847. https://doi.org/10.1016/j.bpj.2010.03.035

Author

Kühnle, Jens ; Shillcock, Julian ; Mouritsen, Ole G. ; Weiss, Matthias. / A modeling approach to the self-assembly of the Golgi apparatus. In: Biophysical Journal. 2010 ; Vol. 98, No. 12. pp. 2839-2847.

Bibtex

@article{366a6855ac624d7bb8025cd95770005f,
title = "A modeling approach to the self-assembly of the Golgi apparatus",
abstract = "The dynamic compartmentalization of eukaryotic cells is a fascinating phenomenon that is not yet understood. A prominent example of this challenge is the Golgi apparatus, the central hub for protein sorting and lipid metabolism in the secretory pathway. Despite major advances in elucidating its molecular biology, the fundamental question of how the morphogenesis of this organelle is organized on a system level has remained elusive. Here, we have formulated a coarse-grained computational model that captures key features of the dynamic morphogenesis of a Golgi apparatus. In particular, our model relates the experimentally observed Golgi phenotypes, the typical turnover times, and the size and number of cisternae to three basic, experimentally accessible quantities: the rates for material influx from the endoplasmic reticulum, and the anterograde and retrograde transport rates. Based on these results, we propose which molecular factors should be mutated to alter the organelle's phenotype and dynamics.",
author = "Jens K{\"u}hnle and Julian Shillcock and Mouritsen, {Ole G.} and Matthias Weiss",
year = "2010",
month = jun,
day = "16",
doi = "10.1016/j.bpj.2010.03.035",
language = "English",
volume = "98",
pages = "2839--2847",
journal = "Biophysical Journal",
issn = "0006-3495",
publisher = "Cell Press",
number = "12",

}

RIS

TY - JOUR

T1 - A modeling approach to the self-assembly of the Golgi apparatus

AU - Kühnle, Jens

AU - Shillcock, Julian

AU - Mouritsen, Ole G.

AU - Weiss, Matthias

PY - 2010/6/16

Y1 - 2010/6/16

N2 - The dynamic compartmentalization of eukaryotic cells is a fascinating phenomenon that is not yet understood. A prominent example of this challenge is the Golgi apparatus, the central hub for protein sorting and lipid metabolism in the secretory pathway. Despite major advances in elucidating its molecular biology, the fundamental question of how the morphogenesis of this organelle is organized on a system level has remained elusive. Here, we have formulated a coarse-grained computational model that captures key features of the dynamic morphogenesis of a Golgi apparatus. In particular, our model relates the experimentally observed Golgi phenotypes, the typical turnover times, and the size and number of cisternae to three basic, experimentally accessible quantities: the rates for material influx from the endoplasmic reticulum, and the anterograde and retrograde transport rates. Based on these results, we propose which molecular factors should be mutated to alter the organelle's phenotype and dynamics.

AB - The dynamic compartmentalization of eukaryotic cells is a fascinating phenomenon that is not yet understood. A prominent example of this challenge is the Golgi apparatus, the central hub for protein sorting and lipid metabolism in the secretory pathway. Despite major advances in elucidating its molecular biology, the fundamental question of how the morphogenesis of this organelle is organized on a system level has remained elusive. Here, we have formulated a coarse-grained computational model that captures key features of the dynamic morphogenesis of a Golgi apparatus. In particular, our model relates the experimentally observed Golgi phenotypes, the typical turnover times, and the size and number of cisternae to three basic, experimentally accessible quantities: the rates for material influx from the endoplasmic reticulum, and the anterograde and retrograde transport rates. Based on these results, we propose which molecular factors should be mutated to alter the organelle's phenotype and dynamics.

UR - http://www.scopus.com/inward/record.url?scp=77953586426&partnerID=8YFLogxK

U2 - 10.1016/j.bpj.2010.03.035

DO - 10.1016/j.bpj.2010.03.035

M3 - Journal article

C2 - 20550896

AN - SCOPUS:77953586426

VL - 98

SP - 2839

EP - 2847

JO - Biophysical Journal

JF - Biophysical Journal

SN - 0006-3495

IS - 12

ER -

ID: 230976550