SWSen Wang

Sen Wang

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


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 publication
  • Josh 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 publication
  • Josh Fnu Arifin

    Department of Chemistry and Biochemistry, California State University Los Angeles, Los Angeles, USA

    1 shared publication
  • Pavle Nikolovski

    Molecular Observatory, California Institute of Technology, Pasadena, USA

    1 shared publication

Latest Publications

  • Antifreeze Protein‐Induced Selective Crystallization of a New Thermodynamically and Kinetically Less Preferred Molecular Crystal

    by Sen Wang, Xin Wen, James A. Golen, Josh F. Arifin, Arnold L. Rheingold

    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.


  • Expanding the molecular recognition repertoire of antifreeze polypeptides: effects on nucleoside crystal growth

    by Sen Wang, Xin Wen, Pavle Nikolovski, Vonny Juwita, Josh Fnu Arifin

    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.