TY - JOUR
T1 - Thickness distribution of actin bundles in vitro
AU - Haviv, Lior
AU - Gov, Nir
AU - Ideses, Yaron
AU - Bernheim-Groswasser, Anne
N1 - Funding Information:
Acknowledgments We would like to thank Samuel Safran for many useful discussions. A.B.G wishes to thank the Joseph and May Winston Foundation Career Development Chair in Chemical Engineering, the Israel Cancer Association (grant No. 20070020B) and the Israel Science Foundation (grant No. 551/04). N.G. wishes to thank the Alvin and Gertrude Levine Career Development Chair and the Israel Science Foundation (grant No. 337/05), for their support.
PY - 2008/4/1
Y1 - 2008/4/1
N2 - Bundles of filamentous actin form the primary building blocks of a broad range of cytoskeletal structures, including filopodia, stereocilia and microvilli. In each case, the cell uses specific associated proteins to tailor the dynamics, dimensions and mechanical properties of the bundles to suit a specific cellular function. While the length distribution of actin bundles was extensively studied, almost nothing is known about the thickness distribution. Here, we use high-resolution cryo-TEM to measure the thickness distribution of actin/fascin bundles, in vitro. We find that the thickness distribution has a prominent peak, with an exponential tail, supporting a scenario of an initial fast formation of a disc-like nucleus of short actin filaments, which only later elongates. The bundle thicknesses at steady state are found to follow the distribution of the initial nuclei indicating that no lateral coalescence occurs. Our results show that the distribution of bundles thicknesses can be controlled by monitoring the initial nucleation process. In vivo, this is done by using specific regulatory proteins complexes.
AB - Bundles of filamentous actin form the primary building blocks of a broad range of cytoskeletal structures, including filopodia, stereocilia and microvilli. In each case, the cell uses specific associated proteins to tailor the dynamics, dimensions and mechanical properties of the bundles to suit a specific cellular function. While the length distribution of actin bundles was extensively studied, almost nothing is known about the thickness distribution. Here, we use high-resolution cryo-TEM to measure the thickness distribution of actin/fascin bundles, in vitro. We find that the thickness distribution has a prominent peak, with an exponential tail, supporting a scenario of an initial fast formation of a disc-like nucleus of short actin filaments, which only later elongates. The bundle thicknesses at steady state are found to follow the distribution of the initial nuclei indicating that no lateral coalescence occurs. Our results show that the distribution of bundles thicknesses can be controlled by monitoring the initial nucleation process. In vivo, this is done by using specific regulatory proteins complexes.
KW - Actin bundles
KW - Cryo-TEM
KW - Non-equilibrium thermodynamics
KW - Thickness distribution
UR - http://www.scopus.com/inward/record.url?scp=41049108021&partnerID=8YFLogxK
U2 - 10.1007/s00249-007-0236-1
DO - 10.1007/s00249-007-0236-1
M3 - Article
C2 - 18004557
AN - SCOPUS:41049108021
SN - 0175-7571
VL - 37
SP - 447
EP - 454
JO - European Biophysics Journal
JF - European Biophysics Journal
IS - 4
ER -