Research


My current research deals with the physics of cellular motility and morphology. I am currently involved in four seperate projects. Overall, my research objectives deal with using physics to understand biological systems. My main interests lie in morphology, propulsion, growth, and fluid dynamics. Though I have mainly done research on cellular-sized objects, I am interested in biophysics at all length scales.

Bacterial gliding motility:

Gliding bacteria have been studied for well over 50 years, but the molecular mechanism that leads to their gliding behavior still remains a mystery. I am currently working with Prof. George Oster (UC Berkeley) on developing a theoretical model that utilizes the swelling of a polyelectrolyte gel (slime) to describe gliding in cyanobacteria and A-motility in Myxococcus xanthus. As well, we are interested in understanding the diverse pattern formation that is seen in multicellular groups of Myxococcus Xanthus. We are working in collaboration with Prof. Dale Kaiser (Stanford), Prof. David Zusman (UC Berkeley), and Dr. Egbert Hoiczyk (Rockefeller) on experiments that can shed more light on the mechanism and guide the theoretical model. The picture to the right shows the volume fraction (color map) of a gel hydrating out of a nozzle structure similar to what was observed by Hoiczyk and Baumeister in cyanobacteria. The arrows show fluid velocity lines.

Supercoiling of filamentous bacteria:

Filamentous bacteria are ubiquitous in nature. Many different species of bacteria form long filaments of end-to-end connected cells when they fail to seperate upon replication. Some species that are seen to do this are B. subtilis, E. coli, and tuberculosis. Under some growth conditions, these filaments will grow to a certain length and then buckle and coil around themselves like an over-twisted phone cord. Neil Mendelson (Arizona) has studied the complex pattern formation that occurs in B. subtilis and has shown what factors affect the morphology. Utilizing elasticity and viscous fluid dynamics, Prof. Thomas Powers (Brown), Prof. Ray Goldstein (University of Arizona), and I have developed a mathematical that describes how growth-induced twist can lead to the supercoiling that is seen in these filaments. Picture to the left shows the numerical solution of the dynamic PDE's for a growing elastic filament loop with preferred twist. The 3-point branches that are seen are similar to what is observed in B. subtilis macrofibers.
The mathematical model mentioned above, does not explain the molecular advent of twist generation during growth. The recent discovery of Mbl and mreB (helical, actin-like cytoskeletal cables in B. subtilis ) suggests a potential mechanism underlying this behavior. George Oster and I recently proposed a quantitative model that describes how growth coupled to helical cytoskeletal proteins can lead to supercoiling. In addition, this model may provide insight into maintenance of form in helical bacteria, such as V. cholerae and C. cresecentus. Now, in collaboration with Prof. Peter Setlow (UCHC), Barabara Setlow (UCHC), and Sulav Mukherjee (UCHC), I have begun to experimentally test this model using a cwlF and sigD filamentous mutant of B. subtilis and fluorescent confocal microscopy. Image to the right shows a coiled mutant with fluorescently label Mbl. This project is supported by NSF MCB 0327716.

Nematode sperm motility:

Utilizing the gel equations that I used to model the slime gun for gliding motility, I hope to show how polymerization and depolymerization of Major Sperm Protein (MSP) can lead to the motility and lamellipod protrusion that is observed in nematode sperm. Beginning with a model developed in collaboration with Prof. George Oster (UC Berkeley) and Prof. Alex Mogilner (UC Davis), Mark Zajac and I are now working on developing a 2D computer simulation to further explore the motility of nematode sperm. In addition, Brian Dacanay, Prof. Bill Mohler (UCHC), Prof. Ann Cowan (UCHC), and I are testing the pH dependence of motility in C. elegans sperm. pH has already been shown to affect crawling in sperm from the nematode Ascaris suum and therefore should play a role in C. elegans . As shown to the left, changes in external pH can reversibly turn on and off the motility of C. elegans spermatozoa. Look here for a movie of crawling nematode sperm.

Spirochete morpholgy and motility

Spirochetes are unique bacteria in that they exist in a helical morphology and their motion is driven by flagella that are encased within their periplasmic space. These bacteria are often highly toxic and exceptionally mobile in gel environments. It has been observed that the cell morphology is dependent on both the cell wall and the flagella. We hope to show how morphology and motility is acheived in these bacteria by studying the coupled elasticity of the cell wall with the flagella. Picture to the right shows Leptospira interrogans.