Boris Rubinstein

ORCID: 0000-0002-0404-3695
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About
Contact & Profiles
Research Areas
  • Cellular Mechanics and Interactions
  • Microtubule and mitosis dynamics
  • Nonlinear Dynamics and Pattern Formation
  • Fluid Dynamics and Thin Films
  • Fungal and yeast genetics research
  • Microfluidic and Bio-sensing Technologies
  • Advanced Mathematical Identities
  • Advanced Combinatorial Mathematics
  • Micro and Nano Robotics
  • Theoretical and Computational Physics
  • Solidification and crystal growth phenomena
  • Mathematical functions and polynomials
  • Genomics and Chromatin Dynamics
  • Acoustic Wave Resonator Technologies
  • Granular flow and fluidized beds
  • Neural Networks and Applications
  • Chromosomal and Genetic Variations
  • nanoparticles nucleation surface interactions
  • 3D Printing in Biomedical Research
  • Gene Regulatory Network Analysis
  • Reproductive Biology and Fertility
  • Plant Reproductive Biology
  • Particle Dynamics in Fluid Flows
  • Pickering emulsions and particle stabilization
  • Cardiomyopathy and Myosin Studies

Stowers Institute for Medical Research
2016-2025

University of Chicago
2023

Kansas City Kansas Community College
2021

New York University
2017

Technion – Israel Institute of Technology
1992-2015

Ural Federal University
2014

University of California, Davis
2003-2007

Northwestern University
2001-2003

Applied Mathematics (United States)
2000-2003

Michigan Technological University
2003

10.1529/biophysj.104.056515 article EN publisher-specific-oa Biophysical Journal 2005-05-07

The Arp2/3 complex nucleates the formation of dendritic actin network at leading edge motile cells, but it is still unclear if plays a critical role in lamellipodia protrusion and cell motility. Here, we differentiated fibroblast cells from isogenic mouse embryonic stem with or without disruption ARPC3 gene, which encodes p21 subunit complex. ARPC3−/− fibroblasts were unable to extend generated dynamic edges composed primarily filopodia-like protrusions, formin proteins (mDia1 mDia2)...

10.1083/jcb.201112113 article EN cc-by-nc-sa The Journal of Cell Biology 2012-04-09
Andrea Guarracino Silvia Buonaiuto Leonardo Gomes de Lima Tamara Potapova Arang Rhie and 95 more Sergey Koren Boris Rubinstein Christian Fischer Haley Abel Lucinda Antonacci-Fulton Mobin Asri Gunjan Baid Carl Baker Anastasiya Belyaeva Konstantinos Billis Guillaume Bourque Andrew Carroll Mark Chaisson Pi-Chuan Chang Xian Chang Haoyu Cheng Justin Chu Sarah Cody Daniel E. Cook Robert Cook‐Deegan Omar E. Cornejo Mark Diekhans Daniel Doerr Peter Ebert Jana Ebler Evan E. Eichler Jordan M. Eizenga Susan Fairley Olivier Fédrigo Adam L. Felsenfeld Xiaowen Feng Paul Flicek Giulio Formenti Adam Frankish Robert S. Fulton Yan Gao Shilpa Garg Nanibaa’ A. Garrison Carlos García Girón Richard E. Green Cristian Groza Leanne Haggerty Ira M. Hall William T. Harvey Marina Haukness David Haussler Simon Heumos Glenn Hickey Kendra Hoekzema Thibaut Hourlier Kerstin Howe Miten Jain Erich D. Jarvis Hanlee P. Ji Eimear E. Kenny Barbara A. Koenig Alexey Kolesnikov Jan O. Korbel Jennifer Kordosky HoJoon Lee Alexandra P. Lewis Heng Li Wen‐Wei Liao Shuangjia Lu Tsung-Yu Lu Julian Lucas Hugo Magalhães Santiago Marco‐Sola Pierre Marijon Charles Markello Tobias Marschall Fergal J. Martin Ann M. Mc Cartney Jennifer McDaniel Karen H. Miga Matthew W. Mitchell Jean Monlong Jacquelyn Mountcastle Katherine M. Munson Moses Njagi Mwaniki Maria Nattestad Adam M. Novak Sergey Nurk Hugh E. Olsen Nathan D. Olson Benedict Paten Trevor Pesout Alice B. Popejoy David Porubský Pjotr Prins Daniela Puiu Mikko Rautiainen Allison Regier Samuel Sacco Ashley D. Sanders

Abstract The short arms of the human acrocentric chromosomes 13, 14, 15, 21 and 22 (SAACs) share large homologous regions, including ribosomal DNA repeats extended segmental duplications 1,2 . Although resolution these regions in first complete assembly a genome—the Telomere-to-Telomere Consortium’s CHM13 (T2T-CHM13)—provided model their homology 3 , it remained unclear whether patterns were ancestral or maintained by ongoing recombination exchange. Here we show that contain...

10.1038/s41586-023-05976-y article EN cc-by Nature 2023-05-10

Polar body extrusion during oocyte maturation is critically dependent on asymmetric positioning of the meiotic spindle, which established through migration meiosis I (MI) spindle/chromosomes from interior to a subcortical location. In this study, we show that MI chromosome biphasic and driven by consecutive actin-based pushing forces regulated two actin nucleators, Fmn2, formin family protein, Arp2/3 complex. Fmn2 was recruited endoplasmic reticulum structures surrounding where it nucleated...

10.1083/jcb.201211068 article EN cc-by-nc-sa The Journal of Cell Biology 2013-02-25

Neurons have a membrane periodic skeleton (MPS) composed of actin rings interconnected by spectrin. Here, combining chemical and genetic gain- loss-of-function assays, we show that in rat hippocampal neurons the MPS is an actomyosin network controls axonal expansion contraction. Using super-resolution microscopy, analyzed localization non-muscle myosin II (NMII). We active NMII light chains are colocalized with organized circular manner throughout axon shaft. In contrast, heavy mostly...

10.7554/elife.55471 article EN cc-by eLife 2020-03-20

Actuation powered by a rotating magnetic field is promising method of controlled steering micro(nano)metric synthetic propellers through fluids. Such actuation relies on torque, which product the driving and dipolar moment possessed micro-/nanopropeller nontrivial shape allowing for rotation–translation coupling. While ferromagnetic (permanently magnetized) microbots have been studied extensively, superparamagnetic (susceptible to magnetization, not possessing remanent magnetization) did get...

10.1063/5.0246571 article EN cc-by Physics of Fluids 2025-01-01

Abstract Despite its widespread existence, the adaptive role of aneuploidy (the abnormal state having an unequal number different chromosomes) has been a subject debate. Cellular associated with enhanced resistance to stress, whereas on organismal level it is detrimental multicellular species. Certain aneuploid karyotypes are deleterious for specific environments, but karyotype diversity in population potentiates evolution. To reconcile these paradoxical observations, this review...

10.1002/bies.201200069 article EN BioEssays 2012-08-24

The ability to break symmetry and polarize through self-organization is a fundamental feature of cellular systems. A prevailing theory in yeast posits that breaking occurs via positive feedback loop, wherein the adaptor protein Bem1 promotes local activation accumulation Cdc42 by directly tethering Cdc42GTP with its guanine nucleotide exchange factor (GEF) Cdc24. In this paper, we find neither nor bind required for cell polarization. Instead, functions primarily boosting GEF activity, role...

10.1083/jcb.201304180 article EN cc-by-nc-sa The Journal of Cell Biology 2013-09-23

We investigate computationally the self-organization and contraction of an initially random actomyosin ring. In framework a detailed physical model for ring cross-linked actin filaments myosin-II clusters, we derive force balance equations solve them numerically. find that to contract, have treadmill be sufficiently cross linked, myosin has processive. The simulations reveal how scales with mechanochemical parameters. For example, they show made longer generates greater but contracts slower....

10.1016/j.bpj.2015.09.013 article EN publisher-specific-oa Biophysical Journal 2015-11-01

The kinetochore is a large, evolutionarily conserved protein structure that connects chromosomes with microtubules. During chromosome segregation, outer components track depolymerizing ends of microtubules to facilitate the separation into two cells. In budding yeast, each has point centromere upon which single built, attaches microtubule. This defined architecture facilitates quantitative examination kinetochores during cell cycle. Using three independent measures—calibrated imaging, FRAP,...

10.1083/jcb.201703152 article EN cc-by The Journal of Cell Biology 2017-09-22

Cells employ protrusive leading edges to navigate and promote their migration in diverse physiological environments. Classical models of leading-edge protrusion rely on a treadmilling dendritic actin network that undergoes continuous assembly nucleated by the Arp2/3 complex, forming ruffling lamellipodia. Recent work demonstrated, however, that, absence fibroblast cells adopt edge with filopodia-like protrusions (FLPs) maintain an ability move, albeit altered responses different...

10.1091/mbc.e14-07-1250 article EN cc-by-nc-sa Molecular Biology of the Cell 2015-01-08
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