Congratulations to Madhurima Das!

Congratulations to Madhurima for a successful defense of her PhD thesis entitled; “Structural Stability and Lipid Interactions in the Misfolding of Human Apolipoprotein A-I: What makes the Protein Amyloidogenic?”

Congratulations to Minjing Liu!

Congratulations to Minjing for a successful defense of her PhD thesis entitled; “Structural Studies of Apolipoprotein A-I and ATP-Binding Cassette A1 and their Roles in Nascent High Density Lipoprotein Biogenesis”.

Nick Frame has his first paper in press!

Structure of Serum Amyloid A Suggests a Mechanism for Selective Lipoprotein Binding and Functions: SAA as a Hub in Macromolecular Interaction Networks” by Nicholas Frame and Olga Gursky has been accepted for publication in FEBS Letters.

A new podcast from PhD candidate Daniel Taub!

A new podcast from PhD candidate Dan Taub, discusses what we learn from model systems. Listen to him tell us about yeast and frogs – more to come. Here’s the link to the podcast.

Madhurima Das is the first co-author in a featured publication in the Journal of Molecular Biology!

Madhurima Das, Christopher J. Wilson, Xiaohu Mei, Thomas E. Wales, John R. Engen, and Olga Gursky, Structural Stability and Local Dynamics in Disease-Causing Mutants of Human Apolipoprotein A-I: What Makes the Protein Amyloidogenic? http://dx.doi.org/10.1016/j.jmb.2015.10.029 The JMB scientific editor writes:” For your featured article, normally we would have a commentary, but since the editor liked the […]

New review article published on cellular membrane and lipid changes that occur upon infection with poliovirus by Jie E. Yang, Evan D. Rossignol, Esther Bullitt

The Role of Electron Microscopy in Studying the Continuum of Changes in Membranous Structures during Poliovirus Infection Viruses 2015, 7(10), 5305-5318; doi:10.3390/v7102874 (registering DOI) http://www.mdpi.com/1999-4915/7/10/2874 Poliovirus infection results in the proliferation of membranous vesicles. The structure and function of these vesicles vary spatially and temporally throughout the viral replication cycle.