Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01GM094588-05
Application #
8730673
Study Section
Special Emphasis Panel (ZGM1-CBB-0)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
5
Fiscal Year
2014
Total Cost
$54,235
Indirect Cost
$19,788
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Bailey, Lucas J; Sheehy, Kimberly M; Hoey, Robert J et al. (2014) Applications for an engineered Protein-G variant with a pH controllable affinity to antibody fragments. J Immunol Methods 415:24-30
Yasui, Norihisa; Findlay, Greg M; Gish, Gerald D et al. (2014) Directed network wiring identifies a key protein interaction in embryonic stem cell differentiation. Mol Cell 54:1034-41
Li, Qufei; Wanderling, Sherry; Paduch, Marcin et al. (2014) Structural mechanism of voltage-dependent gating in an isolated voltage-sensing domain. Nat Struct Mol Biol 21:244-52
Marcon, Edyta; Ni, Zuyao; Pu, Shuye et al. (2014) Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregation. Cell Rep 8:297-310
Welch, Brett D; Paduch, Marcin; Leser, George P et al. (2014) Probing the functions of the paramyxovirus glycoproteins F and HN with a panel of synthetic antibodies. J Virol 88:11713-25
Persson, Helena; Ye, Wei; Wernimont, Amy et al. (2013) CDR-H3 diversity is not required for antigen recognition by synthetic antibodies. J Mol Biol 425:803-11
Paduch, Marcin; Koide, Akiko; Uysal, Serdar et al. (2013) Generating conformation-specific synthetic antibodies to trap proteins in selected functional states. Methods 60:3-14
Rizk, Shahir S; Misiura, Agnieszka; Paduch, Marcin et al. (2012) Substance P derivatives as versatile tools for specific delivery of various types of biomolecular cargo. Bioconjug Chem 23:42-6