Biophysics & Nanoscience @ UT Brownsville
Group Leader:
Andreas Hanke, Assistant
Professor of Physics
Students:
Graduate:
Maria Akhmanova (Ph.D. student at
Marco
Milan
Undergraduate:
Sigrid Andrea Razo
Lauro Salazar
Former students:
Moatez Eldib
Martha Gabriela Ochoa
Erick Vallarino
Mailing Address:
Department of Physics and
80
Office
Address: Engineering, Science
& Technology, Office 1.318
Phone: (956) 882-6682
Fax: (956) 882-6726
e-mail: hanke@phys.utb.edu
Research
Interests: Biophysics and Nanoscience
I am theoretical physicist by training and have
worked in the fields of mesoscopic quantum systems, soft condensed matter
physics, and biological physics. My current plans are to build up a theory
division in the fields of biophysics and nanoscience at the Physics Department
of UT Brownsville. The scope of my research is to develop new theoretical
models relevant to molecular cell biology and nanoscience and to validate these
models with experimental data for systems such as cell membranes, proteins,
DNA, RNA, and their interactions. My research is highly interdisciplinary in
nature, involving Statistical Physics, Biology, Computer Science, and Math.
Casimir
force in nanomechanical systems
Jointly with H. B. Chan (University of Florida)
Student: Lauro Salazar
The increasing miniaturization of nanomechanical
systems requires an understanding of fundamental forces on the nanoscale. When
the distance between metallic or dielectric surfaces is reduced to the
submicron range, forces of pure quantum electrodynamical origin emerge. This
force was first predicted 1948 by H. B. G. Casimir for two infinitely extended,
perfectly conducting, electrically neutral plates in
vacuum. The Casimir force can be understood as resulting from the modification
of the quantum fluctuations of the electromagnetic field in vacuum by the
presence of boundaries. Due to its nature as a fluctuation-induced force, the
Casimir force has a strong dependence on both the geometry and the optical
properties of the interacting bodies.
In 2001, Ho Bun Chan and collaborators at Bell Labs
pioneered experiments that demonstrated the possibility of using the Casimir
force as an actuation force of micromechanical components. These experiments
establish the importance of quantum electrodynamical effects in micro- and
nanomechanical systems (MEMS and NEMS), hence the convergence of fundamental
physics and real world technological applications. Concurrently with this
development, significant progress has been made in the last decade in
predicting the Casimir force for complex geometries and materials, as often
encountered in actual nanomechanical systems.
In this project we calculate the Casimir force for
given material and geometry of nanomechanical components in the framework of
the Lifshitz theory. To this end we use the electromagnetic stress tensor,
which is evaluated via the fluctuation-dissipation theorem in terms of
imaginary-frequency Green’s functions. This approach to calculate the Casimir
force, developed in theory by Dzyaloshinskii in 1961, allows one to resort to
well-developed methods in computational electromagnetics; see Stephen Johnson’s group at MIT and Casimir calculations in Meep.
We currently apply this method to calculate the
Casimir force between a gold-coated sphere and an array of nanoscale
rectangular silicon trenches, for which experimental data are available by Ho Bun Chan’s group [H.
B. Chan et al, Phys. Rev. Lett. 101,
030401 (2008)]. The Green’s function is calculated using finite-difference
methods in the frequency domain (FDFD) and time-domain (FDTD, see Meep). The results will
be validated by experimental data provided by Ho Bun Chan’s group. This project
is a collaboration with the MIT group and Ho Bun Chan.
Setup of the experiment to measure the
Casimir force between a gold
sphere
and a silicon surface with nanoscale trench arrays using a
micromechanical
torsional oscillator [H. B. Chan et al, Phys. Rev. Lett. 101, 030401 (2008)].
Inset: Electron micrograph of the silicon trenches (image courtesy Ho Bun
Chan).
Recent Publications
Andreas Hanke, Casimir force waves induced by non-equilibrium fluctuations between vibrating plates (2009), E-print arXiv:0912.3325
We study the fluctuation-induced, time-dependent force between two plates immersed in a fluid driven out of equilibrium mechanically by harmonic vibrations of one of the plates. Considering a simple Langevin dynamics for the fluid, we explicitly calculate the fluctuation-induced force acting on the plate at rest. The time-dependence of this force is characterized by a positive lag time with respect to the driving, indicating a finite speed of propagation of stress through the medium, reminiscent of waves. We obtain two distinctive contributions to the force, where one may be understood as directly emerging from the corresponding force in the static case, while the other is related to resonant dissipation in the cavity between the plates.
  
Left: Two parallel plates separated by a varying distance L(t). Plate 1 is at rest while plate 2 is vibrating in z-direction.
The plates are immersed in a fluctuating fluid with long-ranged correlations. We are interested in the fluctuation-induced,
time-dependent force F(t) on plate 1.
Right: Force F(t) on plate 1, normalized by its value for plates at rest, for given model parameters (black line).
The harmonic driving of plate 2 is shown as the blue line. For the given parameters, the lag time is 0.15 s, indicating a finite speed
of propagation of the fluctuation-induced force through the medium.
Biophysics
– from single molecules to biological function
Currently I work as Principal Investigator on two
major research projects which are funded by AFOSR (SPRING) and NIH (SCORE) programs:
1) Studies
of single biomolecules: DNA conformational changes and protein binding
Jointly with
S. D. Levene (UT Dallas) and M. C. Williams (Northeastern
University)
Students: Marco Milan, Sigrid Moreno
Structural transitions of DNA and docking of
proteins on DNA are fundamental processes in molecular biology. Understanding
these processes on a single-molecule level is essential for our understanding
of gene function and control, and may find application in DNA-based sensors and
other emerging nanotechnology.
Stretching on individual DNA
molecules in single molecule force spectroscopy can be used to induce a
helix-coil transition in double-stranded DNA. Within a certain range of
stretching forces, only local denaturing of the DNA duplex, or "bubble
formation", occurs. The interaction of these localized regions of unwound
DNA with single-strand-specific DNA binding proteins can then be probed under a
wide range of conditions using new experimental techniques. Our collaborator Mark
Williams and his group at Northeastern University is able to measure the forces
required to stretch single DNA molecules by using an optical tweezers
instrument with high precision. In our lab at UTB we study also force-induced
transitions and conformational changes caused by DNA-binding proteins. A
state-of-the-art Veeco Nanoscope IV Scanning Probe Microscope with PicoForce
Module is available for imaging at atomic resolution and force measurements in
the piconewton range.
2)
Sequence-dependent unwinding in superhelical DNA
Jointly
with S.
D. Levene (UT Dallas)
Sequence-dependent
unwinding of DNA is an integral aspect of many biological processes such as
gene regulation, DNA replication, and DNA repair. DNA unwinding is facilitated by negative
supercoiling, which provides a ubiquitous source of free energy that augments
the unwinding free energy accompanying the interactions of many proteins with
their cognate DNA sequences. Although
much is known about sequence-dependent unwinding in linear DNA molecules, our
present understanding of the effects of supercoiling on localized,
sequence-dependent melting transitions in DNA is at best semi-quantitative.
The
DNA of virtually all terrestrial organisms is negatively supercoiled. Negative
supercoiling is regulated in prokaryotes by DNA gyrase; eukaryotes lack gyrase
but maintain negative supercoiling through winding of DNA around nucleosomes
and interactions with DNA-unwinding proteins.
Large regions of mammalian chromosomes appear to be organized into
negatively supercoiled, topologically independent domains. Therefore,
understanding the interplay of supercoiling and local helical structure is
essential to a complete understanding of biological mechanisms in higher
organisms. Recent developments in
biophysical theory provide an opportunity to develop a detailed and
quantitative framework for analyzing localized DNA-unwinding transitions in
superhelical domains.
In
our research we will use a fusion of numerical simulations of superhelical
conformation and a statistical-mechanical treatment of sequence-dependent
transitions in DNA to develop a comprehensive biophysical model for
supercoiling-dependent DNA unwinding. The
theoretical model will be validated by comparing predictions of the theory for
several DNA sequences with experimental data from plasmid DNAs and supercoiled
DNA minicircles that contain 2-aminopurine substitutions as spectroscopic
probes of local unwinding.
Recent Publications
[1] R. Metzler, T. Ambjornsson, A. Hanke, and H. C. Fogedby, Single DNA denaturation and bubble dynamics, J. Phys.: Condens. Matter 21, 034111 (2009).
[2] L. Shokri, B. Marintcheva, M. Eldib, A. Hanke, I. Rouzina, and M. C. Williams, Kinetics and thermodynamics of salt-dependent T7 gene 2.5 protein binding to single- and double-stranded DNA, Nucl. Acids Res. 36, 5668 (2008).
[3] A. Hanke, Martha G. Ochoa, and R. Metzler, Denaturation transition of stretched DNA, Phys. Rev. Lett. 100, 018106 (2008); E-print arXiv:0709.2958.
[4] R. Metzler, T. Ambjornsson, A. Hanke, and S. Levene, Single DNA conformations and biological function, Review article, J. Comp. Theor. Nanoscience 4, 1 (2007); E-print physics/0609139.
Development
I wrote my diploma thesis with Prof. W. Zwerger at
the Physics Department at the Ludwig Maximilians
University Munich,
Teaching
F 2004: PHYS 5321 - Classical Mechanics (Graduate
Course)
S 2005: PHYS 4320 - Quantum Mechanics (Undergraduate
Course)
F 2005: PHYS
5322 – Electrodynamics II (Graduate Course at UT
S 2006: PHYS 4380
– Thermodynamics and Statistical Mechanics
(Undergraduate Course)
F
2006: PHYS 5461 – Quantum Mechanics (Graduate Course)
S 2007: PHYS
1302 – General Physics II (Undergraduate Course)
F 2007: PHYS 5364
– Thermodynamics and Statistical Mechanics
(Graduate Course)
S 2008: PHYS
5321 – Classical
Mechanics (Graduate Course)
F 2009: PHYS 1302 – General
Physics II (Undergraduate Course)
S 2009: PHYS
3320 – Thermodynamics and Statistical Mechanics (Undergraduate Course)
F 2009: PHYS
5330 – Thermodynamics and Statistical Mechanics (Graduate Course)