Category Archives: Soft Matter

Fundamentals of Soft matter science 2nd Ed – out now!

Summary

This revised edition continues to provide the most approachable introduction to the structure, characteristics, and everyday applications of soft matter. It begins with a substantially revised overview of the underlying physics and chemistry common to soft materials. Subsequent chapters comprehensively address the different classes of soft materials, from liquid crystals to surfactants, polymers, colloids, and biomaterials, with vivid, full-color illustrations throughout. There are new worked examples throughout, new problems, some deeper mathematical treatment, and new sections on key topics such as diffusion, active matter, liquid crystal defects, surfactant phases and more.

• Introduces the science of soft materials, experimental methods used in their study, and wide-ranging applications in everyday life.

• Provides brand new worked examples throughout, in addition to expanded chapter problem sets and an updated glossary.

• Includes expanded mathematical content and substantially revised introductory chapters. 

This book will provide a comprehensive introductory resource to both undergraduate and graduate students discovering soft materials for the first time and is aimed at students with an introductory college background in physics, chemistry or materials science. 

New NSF grant – mixing in active matter

The Hirst Lab has been awarded a new three-year NSF grant along with collaborator UC Merced’s Kevin Mitchell.

The grant, combining experiment and theory is titled “Self-mixing Active Fluids”

Abstract

Active matter is one of the most exciting frontiers in soft matter science. Unlike typical fluids, active fluids are not in equilibrium. Instead, they consume energy locally, translating this energy into internal flows and spontaneous mixing. In this project, mass transport and chaotic mixing in active fluids will be investigated using a fluid consisting of microtubules and kinesin, biological molecules found in the cell. Densely packed microtubules slide antiparallel to each other at a controlled rate due to coupled kinesin molecular motors. An exciting outcome of this work could be the development of a new class of self-mixing active solvents. Such a solvent could revolutionize our understanding of the kinetics of mass transport and chemical reactions. The present proposal concerns much larger length scales than that of standard solvents and will thus serve as an experimental model for these new ideas, helping to establish fundamental laws that govern the behavior of active matter. Since the contents of biological cells are highly complex active materials, far from equilibrium, this work is expected to yield new insights into the role of active materials in biology. A proposed Telluride workshop on transport in active fluids will help to bring together the relatively disparate fields of liquid crystals, biological fluids and nonlinear dynamics. This work will have a significant educational impact at UC Merced, a new university in one of California’s most socio-economically disadvantaged areas. This research will provide the basis for several undergraduate theses and the PIs will use insights from this work to introduce cutting edge materials to their graduate and undergraduate teaching.

This project focuses on transport and mixing in a biologically inspired extensile active nematic. Densely packed microtubules slide antiparallel to each other at a controlled rate due to kinesin molecular motors and the resulting chaotic advection will be measured on different length scales, using the experimental tools of particle tracking, particle image velocimetry, and fluorescence imaging of labeled tracers. Experimental data will be theoretically interpreted using the tools of nonlinear and topological dynamics, thereby merging the fields of chaotic advection and liquid crystals in a unique collaborative effort. Topological entropy will play a central, unifying role in this study. Topological entropy is well known in studies of chaotic advection, but has been thus far overlooked in studies of active nematics. Specific aims are to: 1) use bead tracking and velocity reconstruction, together with tools from nonlinear dynamics, to measure the topological entropy of active nematic mixing; 2) measure the effective diffusivity, enhanced by chaotic advection, of the active nematic on the macroscale; and 3) investigate correlations between molecular-scale dynamics, mesoscale mixing, and macroscale diffusion by varying system parameters.

Congratulations Dr Melton!

Nathan Melton, our most recent graduate walked at UC Merced commencement this month. Nathan’s recent work, focused on topological defects in liquid crystals with a new paper just out last month in the journal Nanomaterials.

“Phase-transition-driven nanoparticle assembly in liquid crystal droplets” Charles N. Melton, Sheida T. Riahinasab, Amir Keshavarz, Benjamin J. Stokes and Linda S. Hirst, Nanomaterials, 8, 146 (2018). Link

Dr Melton and Dr Hirst

Nathan has already started work as a postdoctoral scientist at Lawrence Berkeley National Lab at the Advanced Light Source!

Active Matter in Biology:Nature News and Views

Recently Prof Hirst authored a News and Views in Nature focussed on two exciting articles about the cell epithelium as active matter.

“Evidence has been found that a biological tissue might behave like a liquid crystal. Even more remarkably, topological defects in this liquid-crystal system seem to influence cell behaviour. A materials physicist and a biologist discuss what the findings mean for researchers in their fields”.

Read the full article here

Biological physics: Liquid crystals in living tissue

 

Studying microtubule spools

Understanding the role of transport velocity in biomotor-powered microtubule spool assembly

Amanda J. Tan, Dail E. Chapman, Linda S. Hirst and Jing Xu

In this new paper we examined the sensitivity of microtubule spools to transport velocity.
Perhaps surprisingly, we determined that the steady-state
number and size of spools remained constant over a seven-fold
range of velocities. Our data on the kinetics of spool assembly
further suggest that the main mechanisms underlying spool growth
vary during assembly.
Read the paper in RSC Advances here

Amanda Tan – winner 2016 faculty mentor fellowship

Congratulations to physics graduate student Amanda Tan for winning a UC Merced “faculty mentor” fellowship.  This prestigious fellowship is awarded to prepare future faculty and provides a year’s funding plus a travel stipend.

Amanda’s research project focuses on active biological materials, in particular microtubules and molecular motors. She is collaborating with the Xu lab at UC Merced and will have her first paper with the group out soon.

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The award assists recipients in acquiring and developing advanced research skills under faculty mentorship and is aimed at increasing the number of students who complete their Ph.D. degree and successfully acquire a faculty appointment.

 

 

Using molecular motors to extract lipid tubules

A Simple Experimental Model to Investigate Force Range for Membrane Nanotube Formation

Chai Lor1, Joseph D. Lopes2, Michelle K. Mattson-Hoss3, Jing Xu2* and Linda S. Hirst2*
  • 1Biological Engineering and Small-scale Technologies Graduate Program, School of Engineering, University of California Merced, Merced, CA, USA
  • 2Physics Department, School of Natural Science, University of California Merced, Merced, CA, USA
  • 3Developmental and Cell Biology, School of Biological Sciences, University of California Irvine, Irvine, CA, USA

fmats-03-00006-g001The presence of membrane tubules in living cells is essential to many biological processes. In cells, one mechanism to form nanosized lipid tubules is via molecular motor induced bilayer extraction. In this paper, we describe a simple experimental model to investigate the forces required for lipid tube formation using kinesin motors anchored to 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) vesicles. Previous related studies have used molecular motors actively pulling on the membrane to extract a nanotube. Here, we invert the system geometry; molecular motors are used as static anchors linking DOPC vesicles to a two-dimensional microtubule network and an external flow is introduced to generate nanotubes facilitated by the drag force. We found that a drag force of ≈7 pN was sufficient for tubule extraction for vesicles ranging from 1 to 2 μm in radius. By our method, we found that the force generated by a single molecular motor was sufficient for membrane tubule extraction from a spherical lipid vesicle.