

183
Biophysical Society 59
th
Annual Meeting, Baltimore, Maryland
Room A: Monday, February 9
9:30
am
–11:00
am
Pall ForteBio LLC
Measuring Engineered Changes in Binding Affinity with the BLItz®
Label-Free System
Combining Organic Synthesis and Directed Evolution to Design Glycocluster
HIV Vaccine Candidates
We will describe a new method for design of carbohydrate HIV vaccines,
which combines organic synthesis and directed evolution techniques. This
work originates from the observation that some HIV positive individuals
produce antibodies which are broadly neutralizing and protective against
HIV infection. One such antibody, 2G12, recognizes and binds to a
cluster of carbohydrates on the viral envelope protein gp120. Our goal is
to develop synthetic carbohydrate clusters which closely mimic the viral
carbohydrate cluster, and which might thus elicit a 2G12-like antibody
response when used as a vaccine. In order to design carbohydrate clusters
which closely mimic gp120, we have developed evolution-based strategies,
in which immobilized 2G12 is used to recognize and fish out the best gly-
cocluster mimics of gp120 from amongst large libraries of ~10 trillion dif-
ferent glycosylated peptide- or DNA structures. The glycocluster structures
obtained by these methods are recognized by antibody 2G12 as strongly as
is the viral protein itself, and are thus of great interest for vaccine studies.
Tips and Tricks for Developing BLItz Assays
The BLItz label-free assay system is a simple-to-use benchtop instrument
for measuring binding interactions of antibodies and proteins using as little
as 4µl of sample. Additional case studies of how the BLItz system is being
used to qualify biophysical models will be presented, along with tips and
tricks for developing kinetics assays on the BLItz system.
Presenters
Isaac Krauss, Assistant Professor of Chemistry, Brandeis University
Craig Tin, Senior Product Manager, Pall Forte Bio LLC
11:30
am
–1:00
pm
Asylum Research, an Oxford Instruments Company
There’s No Other AFM Like Cypher™
—
High Resolution Atomic
Force Microscopy Made Easier and Faster
Asylum Research has focused on improving AFM instrumentation to
make imaging in liquid easier, faster and more quantitative for life sci-
ence applications. Please join us for this 'Lunch and Learn' presentation
that will focus on the latest technical advances in AFM that enable high
resolution imaging of the structure and dynamics of samples including
proteins, lipids and nucleic acids. We’ll show examples of how the Cypher
ES Environmental AFM allows users to control the environment around
their sample and perform perfusion experiments easily. You’ll learn about
Cypher’s numerous ease-of-use features such as GetStarted™, GetReal™,
and blueDrive™ for easy and stable imaging in liquid. We will introduce
you to Fast Force Mapping, our unique technology that measures mechan-
ical properties of your samples faster and more reliably. This is also a great
opportunity to ask our scientists any questions you may have about AFM.
Presenter
Irène Revenko, Applications Scientist, Asylum Research, an Oxford
Instruments Company
1:30
pm
–3:00
pm
World Precision Instruments
Side-Stepping the Animal Model: Cardiac Work Loops in Human
iPSC-derived Myocytes.
Cardiac pressure-volume loops on a complete organ provide the frame-
work for understanding cardiac mechanics in experimental animal models,
most notably in the context of Frank-Starling mechanisms. With the
development of more sensitive transducers, this work has been applied to
single cardiac cells, using freshly isolated cells from an animal model. With
the advent of iPSC-derived myocytes, a whole new range of cell types is
now available to the investigator. We introduce a novel mounting applica-
tion for overcoming the technical difficulties in instrumenting these cells
for force measurements. With this technology, it is now possible to conduct
experiments on human stem cell-derived myocytes.
We will show preliminary results, the tools required for these types of
experiments, mounting methods, and a novel method for direct force
measurements on human iPSC-derived myocytes. In addition, two dif-
ferent methods for real-time determination of length changes in isolated
iPSC-derived myocytes will be presented. The results are preliminary,
however indicate the possibility for not only a reduction in the use of
the animal models in cardiac research, but also the direct investigation of
human cardiovascular disease.
3:30
pm
–5:00
pm
Bruker Nano Surfaces
Recent Advances in Atomic Force Microscopy for Biological Research
Bruker’s latest BioScope AFM is the perfect integration of AFM and invert-
ed light microscopy. It incorporates Bruker’s latest Peak Force Tapping
innovations including the new nanomechanics package, which signifi-
cantly expands mechanobiology applications into a lower modulus range
covering live cells and tissues. With its open access design, and bio friendly
features and accessories, the latest BioScope AFM is the most integrated
and easiest to use life science AFM available. The workshop will include
examples of the functional integration of light microscopy techniques
with AFM in order to conduct optically guided, high-resolution mapping
of both the structural and mechanical properties of mammalian cells.
Presenter
John Thornton, Senior Applications Engineer, Bruker Nano Surfaces
5:30
pm
–7:00
pm
HEKA Elektronik
HEKA Electrophysiology Update
For over 40 years, HEKA has provided innovative products, expert tech
support and unmatched service to their customers. HEKA's commitment
to technological innovation is reflected by consistent updating of both
hardware and software. While yesterday's gold standards try to keep pace
with the latest research techniques, HEKA takes the lead.
By popular demand, HEKA is hosting a series of user meetings with
tutorial presentations. On one hand, some of the new products will be
showcased to the experienced user and, on the other hand, step-by-step
guidance is provided to the researcher who is new to the field. Registration
is available online through the HEKA Events Page on EventBrite, or by