Cell biology -- new insights into the life of microtubules

Public release date: 2-Jul-2012
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Contact: Dr. Kathrin Bilgeri
kathrin.bilgeri@lmu.de
49-892-180-6938
Ludwig-Maximilians-Universitt Mnchen

Every second, around 25 million cell divisions take place in our bodies. This process is driven by microtubule filaments which continually grow and shrink. A new study shows how so-called motor proteins in the cytosol can control their dynamics.

The cytoskeleton plays a central role in the process of cell division. It is composed in large part of protein filaments known as microtubules, which also help determine the size, shape and mobility of a cell. In a new study, LMU biophysicist Erwin Frey and his colleagues Anna Melbinger and Louis Reese have used a theoretical model to show how cells control the construction and breakdown of microtubules. The dy-namics of this process affect how cells divide, and how they maintain the cytoskeleton. In particular, it is responsible for regulating the size and shape of the mitotic spindle.

Easy come, easy go

Theoretical modeling has now revealed that the regulation of microtubule length relies on the length of the filament itself: The longer the filament the more motor proteins can attach to it. These all move towards the 'plus end' of the microtubule and tend to pile up as they do so. Upon arrival at the plus-end they shorten the filament. In parallel, new microtubule building blocks bind to precisely the same 'plus end' through spontaneous polymerization from the surrounding cytosol, and the filament grows.

It has now been demonstrated that such interplay between growth and length-dependent shrinkage indeed results in the maintenance of a precisely regulated microtubule length. This kind of length regulation might be essential for many intracellular tasks which depend on microtubules of a certain length. (Physical Review Letters, 22. June 2012)

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This work was supported by the Cluster of Excellence "Nanosystems Initiative Munich" (NIM) and SFB 863 (Forces in Biomolecular Systems)

Publication:
Microtubule Length Regulation by Molecular Motors
Anna Melbinger, Louis Reese, and Erwin Frey
Phys. Rev. Lett. 108, 258104 (2012). Published online June 22, 2012

Contact:
Prof. Dr. Erwin Frey
Chair of Statistical and Biological Physics
Arnold Sommerfeld Center for Theoretical Physics, Center for NanoScience (CeNS) and the Cluster of Excellence "Nanosystems Initiative Munich" (NIM)
LMU Munich

Phone: +49 89 / 2180 4537
Fax: +49 89 / 2180 4538
Email: frey@lmu.de
Web: www.theorie.physik.uni-muenchen.de/lsfrey/group_frey

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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

Public release date: 2-Jul-2012
[ | E-mail | Share ]

Contact: Dr. Kathrin Bilgeri
kathrin.bilgeri@lmu.de
49-892-180-6938
Ludwig-Maximilians-Universitt Mnchen

Every second, around 25 million cell divisions take place in our bodies. This process is driven by microtubule filaments which continually grow and shrink. A new study shows how so-called motor proteins in the cytosol can control their dynamics.

The cytoskeleton plays a central role in the process of cell division. It is composed in large part of protein filaments known as microtubules, which also help determine the size, shape and mobility of a cell. In a new study, LMU biophysicist Erwin Frey and his colleagues Anna Melbinger and Louis Reese have used a theoretical model to show how cells control the construction and breakdown of microtubules. The dy-namics of this process affect how cells divide, and how they maintain the cytoskeleton. In particular, it is responsible for regulating the size and shape of the mitotic spindle.

Easy come, easy go

Theoretical modeling has now revealed that the regulation of microtubule length relies on the length of the filament itself: The longer the filament the more motor proteins can attach to it. These all move towards the 'plus end' of the microtubule and tend to pile up as they do so. Upon arrival at the plus-end they shorten the filament. In parallel, new microtubule building blocks bind to precisely the same 'plus end' through spontaneous polymerization from the surrounding cytosol, and the filament grows.

It has now been demonstrated that such interplay between growth and length-dependent shrinkage indeed results in the maintenance of a precisely regulated microtubule length. This kind of length regulation might be essential for many intracellular tasks which depend on microtubules of a certain length. (Physical Review Letters, 22. June 2012)

###

This work was supported by the Cluster of Excellence "Nanosystems Initiative Munich" (NIM) and SFB 863 (Forces in Biomolecular Systems)

Publication:
Microtubule Length Regulation by Molecular Motors
Anna Melbinger, Louis Reese, and Erwin Frey
Phys. Rev. Lett. 108, 258104 (2012). Published online June 22, 2012

Contact:
Prof. Dr. Erwin Frey
Chair of Statistical and Biological Physics
Arnold Sommerfeld Center for Theoretical Physics, Center for NanoScience (CeNS) and the Cluster of Excellence "Nanosystems Initiative Munich" (NIM)
LMU Munich

Phone: +49 89 / 2180 4537
Fax: +49 89 / 2180 4538
Email: frey@lmu.de
Web: www.theorie.physik.uni-muenchen.de/lsfrey/group_frey

---

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AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.

Source: http://www.eurekalert.org/pub_releases/2012-07/lm-cb-070212.php

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