Sen Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Sen Wang has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Xin Wen
Department of Chemistry and Biochemistry, California State University Los Angeles, Los Angeles, CA 90032, USA
2 shared publications - Arnold L. Rheingold
University of California San Diego
1 shared publication James A. Golen
[c]Department of Chemistry and Biochemistry University of California, San Diego, La Jolla, CA 92093 (USA)
1 shared publicationJosh F. Arifin
[b]Department of Chemistry and Biochemistry, California State University, Los Angeles, 5151 State University Drive, Los Angles 90032 (USA), Fax: (+1)323-343-6490
1 shared publicationJosh Fnu Arifin
Department of Chemistry and Biochemistry, California State University Los Angeles, Los Angeles, USA
1 shared publicationPavle Nikolovski
Molecular Observatory, California Institute of Technology, Pasadena, USA
1 shared publication
Latest Publications
- 9 October 2013
- Published by Wiley in Chemistry – A European Journal
- Vol. 19 (47) , 16104-16112
Antifreeze Protein‐Induced Selective Crystallization of a New Thermodynamically and Kinetically Less Preferred Molecular Crystal
The formation of a new, dihydrate crystalline form of 5‐methyluridine (m5U) was selectively induced by a protein additive, antifreeze protein (AFP) in a highly efficient manner (in 10−6 molar scale, whereas known kinetic additives need 0.1 molar scale). The hemihydrate form (form I, the only previously known crystalline form of m5U) and the dihydrate form of m5U (form II) obtained herein were characterized using X‐ray crystallography and differential scanning calorimetry (DSC). Compared to form I, remarkably, form II is thermodynamically and kinetically less preferred. The presence of AFP can selectively inhibit the appearance of form I and hence allows the growth of form II, the pure form of which cannot grow directly from m5U supersaturated solutions under the same conditions. An explanation supported by both experimental and theoretical results is provided for the AFP‐induced selection process. Implications on AFP‐induced ice shape changes are also discussed. Control of crystallization from supersaturated solutions is of great interest in both fundamental research and practical applications in fields like chemistry, pharmacology and materials science. These findings suggest that crystallization processes with AFPs could be valuable for selective growth of hydrates and polymorphs of important pharmaceutical compounds.
- 9 October 2013
- Published by Wiley in Chemistry – A European Journal
- Vol. 19 (47) , 16104-16112
Antifreeze Protein‐Induced Selective Crystallization of a New Thermodynamically and Kinetically Less Preferred Molecular Crystal
The formation of a new, dihydrate crystalline form of 5‐methyluridine (m5U) was selectively induced by a protein additive, antifreeze protein (AFP) in a highly efficient manner (in 10−6 molar scale, whereas known kinetic additives need 0.1 molar scale). The hemihydrate form (form I, the only previously known crystalline form of m5U) and the dihydrate form of m5U (form II) obtained herein were characterized using X‐ray crystallography and differential scanning calorimetry (DSC). Compared to form I, remarkably, form II is thermodynamically and kinetically less preferred. The presence of AFP can selectively inhibit the appearance of form I and hence allows the growth of form II, the pure form of which cannot grow directly from m5U supersaturated solutions under the same conditions. An explanation supported by both experimental and theoretical results is provided for the AFP‐induced selection process. Implications on AFP‐induced ice shape changes are also discussed. Control of crystallization from supersaturated solutions is of great interest in both fundamental research and practical applications in fields like chemistry, pharmacology and materials science. These findings suggest that crystallization processes with AFPs could be valuable for selective growth of hydrates and polymorphs of important pharmaceutical compounds.
- 15 October 2012
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 48 (94) , 11555-11557
Expanding the molecular recognition repertoire of antifreeze polypeptides: effects on nucleoside crystal growth
Despite differences in the crystal structures of ice and nucleosides, antifreeze polypeptides (AFPs) have been demonstrated to inhibit nucleation of 5-methyluridine, cytidine, and inosine and modify the crystal growth of the nucleosides efficiently. The molecular recognition repertoire of AFPs has been expanded to non-ice-like crystalline solids.
- 15 October 2012
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 48 (94) , 11555-11557
Expanding the molecular recognition repertoire of antifreeze polypeptides: effects on nucleoside crystal growth
Despite differences in the crystal structures of ice and nucleosides, antifreeze polypeptides (AFPs) have been demonstrated to inhibit nucleation of 5-methyluridine, cytidine, and inosine and modify the crystal growth of the nucleosides efficiently. The molecular recognition repertoire of AFPs has been expanded to non-ice-like crystalline solids.