Analysis of T lymphocyte activation measured by Super-Resolution Microscopy
ORAL
Abstract
Tight regulatory control of the activation signal in T lymphocytes is necessary to prevent the immune response from getting too large or persisting too long. Utilizing cutting-edge super-resolution imaging technologies in combination with quantitative image analysis, we explore one aspect of this regulation in activated cells: the dynamics of the protein MALT1. Our goal is to analyze how the motion of MALT1 within the cell affects the transduction and regulation of the activation signal. A focus of our analysis is to measure anisotropies in the spatial organization of MALT1 and the shape of the related larger scale protein complex that it is a part of, the POLKADOTS Signalosome.
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Authors
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Leonard Campanello
University of Maryland at College Park
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Maria Traver
Uniformed Services University of the Health Sciences
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Hari Schroff
National Institute of Biomedical Imaging and Bioengineering
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Brian Schaefer
Uniformed Services University of the Health Sciences
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Wolfgang Losert
University of Maryland College Park, Univ of Maryland-College Park, University of Maryland at College Park