Antifreeze proteins (AFPs) have been identified in a number of organisms, such as fish, plants, and insects, to allow them to survive at subfreezing temperatures. They are all characterized by their ability to depress the freezing point of the solution without appreciably altering the melting point thereby producing a thermal hysteresis. Insect AFPs are often the most active AFPs (10-100 times more active than type I fish AFPs). Enhancers have been identified in AFPs from the beetle Dendroides canadensis (DAFPs) to achieve the optimal antifreeze activity of DAFP. Citrate is the best enhancer that has been identified for DAFPs so far. Although many low molecular weight enhancers have been identified and some of them do play a role in enhancing the antifreeze activity of DAFPs physiologically, the molecular mechanism(s) of the enhancer(s) is not well developed. The study of AFPs and enhancers is essential to advance our understanding of the biological system and facilitate their potential biomedical applications, such as cryopreservation and cryosurgery, and many other applications (e.g., in frozen foods). In this project, we will correlate the structures with the physicochemical properties of selected citrate derivatives. We propose that the efficiency of enhancers on DAFP antifreeze activity depends on the physiochemical properties of the enhancers. We will characterize the enhancement efficiency of selected citrate derivatives on DAFP antifreeze activity and investigate how the enhancement efficiency of the systematically varied citrate derivatives varies with their differing physicochemical properties. To reveal the insights of the molecular mechanism of low molecular weight enhancers, we will then explore the possible interactions among the enhancers, DAFP, and ice. A molecular basis for identifying and rationally designing highly efficient enhancers can be thereby developed. This proposed project offers a new approach to the mechanistic study of AFP enhancers. In addition, the delineation of the molecular mechanism of AFP enhancers will resolve conflicts among published mechanisms of AFPs. The proposed study of AFPs and enhancers is essential to advance our understanding of the biological system. The results of the study will contribute to public health in facilitating the potential biomedical applications of AFPs and enhancers such as in longer storage of transplant organs, cryopreservation, and cryosurgery, and many other applications (e.g., in frozen foods).

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Continuance Award (SC3)
Project #
5SC3GM086249-02
Application #
7749942
Study Section
Special Emphasis Panel (ZGM1-MBRS-X (CH))
Program Officer
Okita, Richard T
Project Start
2009-01-01
Project End
2011-12-31
Budget Start
2010-01-01
Budget End
2010-12-31
Support Year
2
Fiscal Year
2010
Total Cost
$108,375
Indirect Cost
Name
California State University Los Angeles
Department
Type
Schools of Arts and Sciences
DUNS #
066697590
City
Los Angeles
State
CA
Country
United States
Zip Code
90032
Wen, Xin; Wang, Sen; Duman, John G et al. (2016) Antifreeze proteins govern the precipitation of trehalose in a freezing-avoiding insect at low temperature. Proc Natl Acad Sci U S A 113:6683-8
Wang, Sen; Wen, Xin; DeVries, Arthur L et al. (2014) Molecular recognition of methyl ?-D-mannopyranoside by antifreeze (glyco)proteins. J Am Chem Soc 136:8973-81
Wang, Sen; Wen, Xin; Golen, James A et al. (2013) Antifreeze protein-induced selective crystallization of a new thermodynamically and kinetically less preferred molecular crystal. Chemistry 19:16104-12
Wang, Sen; Amornwittawat, Natapol; Wen, Xin (2012) Thermodynamic Analysis of Thermal Hysteresis: Mechanistic Insights into Biological Antifreezes. J Chem Thermodyn 53:125-130
Wang, Sen; Wen, Xin; Nikolovski, Pavle et al. (2012) Expanding the molecular recognition repertoire of antifreeze polypeptides: effects on nucleoside crystal growth. Chem Commun (Camb) 48:11555-7
Wen, Xin; Wang, Sen; Amornwittawat, Natapol et al. (2011) Interaction of reduced nicotinamide adenine dinucleotide with an antifreeze protein from Dendroides canadensis: mechanistic implication of antifreeze activity enhancement. J Mol Recognit 24:1025-32
Wang, Sen; Amornwittawat, Natapol; Banatlao, Joseph et al. (2009) Hofmeister effects of common monovalent salts on the beetle antifreeze protein activity. J Phys Chem B 113:13891-4
Wang, Sen; Amornwittawat, Natapol; Juwita, Vonny et al. (2009) Arginine, a key residue for the enhancing ability of an antifreeze protein of the beetle Dendroides canadensis. Biochemistry 48:9696-703
Amornwittawat, Natapol; Wang, Sen; Banatlao, Joseph et al. (2009) Effects of polyhydroxy compounds on beetle antifreeze protein activity. Biochim Biophys Acta 1794:341-6