<?xml version="1.0" encoding="UTF-8"?><profile href="/about_us/FacultyDirectory/MicrobiologyBiochemistryImmunology/VincentBond/index.php">
   <image><img src="/_resources/MSMimages/FacultyDirectoryImages/MBI/Bond.jpg" alt="Vincent C. Bond, BS, MS, Ph.D."></img></image>
   <name>Vincent C. Bond, BS, MS, Ph.D.</name>
   <title>Professor Emeritus</title>
   <department>Microbiology, Biochemistry &amp; Immunology</department>
   <email>vbond@msm.edu</email>
   <title2></title2>
   <department2></department2>
   <phone></phone>
   <location></location>
   <education><strong>POSTGRADUATE:</strong><br></br>California Institute of Technology<br></br><strong>Fellowship:</strong> Postdoctoral <br></br><br></br><strong>GRADUATE:</strong><br></br>Pennsylvania State University<br></br><strong>Degree: </strong>Doctor of Philosophy in Genetics <br></br><br></br>Pennsylvania State University<br></br><strong>Degree: </strong>Master of Science in Genetics<br></br><br></br><strong>UNDERGRADUATE:</strong><br></br>Pennsylvania State University<br></br><strong>Degree: </strong>Bachelor of Science in Biology</education>
   <research>
      <p>Our research integrates virology, cancer biology, and microbial pathogenesis within
         the field of natural products–inspired therapeutics. We have identified the HIV Nef
         secretion modification region (SMR), engineered into a bioactive peptide that functions
         as a Short Linear Motif (SLiM) targeting host chaperones and extracellular vesicle
         pathways. This SMR-derived peptide reveals conserved mechanisms linking viral modulation,
         tumorigenesis, and bacterial biofilm formation, including demonstrated disruption
         of E. coli and MRSA biofilms. These findings suggest the SMR exploits evolutionarily
         conserved cellular processes, positioning it as a novel natural product–like scaffold
         with broad therapeutic potential.</p>
   </research>
   <boardcerts></boardcerts>
   <publications>
      <p><a title="Publications Link" href="https://www.ncbi.nlm.nih.gov/sites/myncbi/vincent.bond.1/bibliography/40007995/public/?page=1#main_content%20">Publications Link</a><br></br><br></br>Shelton MN, Huang MB, Ali SA, Powell MD, and <strong>Bond VC.</strong> 2012. SMR-derived peptide disrupts HIV-1 Nef’s interaction with mortalin and blocks
         virus and Nef exosome release. J Virol. Jan, 86(1): 406-19. PMC3255900.<br></br><br></br>Kim DK, Lee J, Kim SR, et al. 2013.  EVpedia: A Community Web Portal for Extracellular
         Vesicles Research. Bioinformatics. doi:10.1093/bioinformatics/btu741. PMC4375401.<br></br><br></br>Konadu KA, Chu J, Huang MB, Amancha PK, Armstrong W, Powell MD, Villinger F, <strong>Bond VC</strong>. 2014. Cytokines Associate with Exosomes in the Plasma of HIV-1+ Individuals. Journal
         of Infectious Diseases. doi: 10.1093/infdis/jiu676. PMC4447830</p>
      <p> </p>
      <p>Konadu KA, Anderson JS, Huang MB, Ali SA, Powell MD, Villinger F, Bond VC. 2015. Hallmarks
         of HIV-1 pathogenesis are modulated by Nef’s Secretion Modification Region. J AIDS
         Clin Res Jul; 6(7). pii: 476. Epub 2015 Jun 30. PMC4625552.</p>
      <p> </p>
      <p>Konadu KA, Huang MB, Roth W, Armstrong W, Powell M, Villinger F, Bond VC. 2016. Isolation
         of Exosomes from the Plasma of HIV-1 Positive Individuals. J Vis Exp. 2016 Jan 5;(107).
         doi: 10.3791/53495. PMC4780996</p>
      <p> </p>
      <p>Huang MB, Gonzalez RR, Lillard J, Bond VC. Secretion Modification Region-Derived Peptide
         Blocks Exosome Release and Mediates Cell Cycle Arrest in Breast Cancer Cells. OncoTarget.
         2017, Jan 5.  doi: 10.18632/oncotarget.14513. PMC5355266</p>
      <p>Click <a href="http://www.ncbi.nlm.nih.gov/sites/myncbi/vincent.bond.1/bibliography/40007995/public/?sort=date&amp;direction=ascending">here</a> to view additional publications.<br></br><br></br></p>
      <p><strong><span style="text-decoration: underline;">Patents</span></strong></p>
      <p>Bond, VC, Lillard JW, Huang, MB. USP10,040,831 B2. 08/07/18. Compositions and methods
         for treating diseases by inhibiting exosome release. <a href="http://patft.uspto.gov/netahtml/PTO/srchnum.htm">http://patft.uspto.gov/netahtml/PTO/srchnum.htm</a>  </p>
      <p>Bond VC, Powell M, Huang MB, Ali S., Shelton MN. USP 8,669,226. 03/11/14. Antimicrobial
         compositions and methods of use thereof. <a href="http://patft.uspto.gov/netahtml/PTO/srchnum.htm">http://patft.uspto.gov/netahtml/PTO/srchnum.htm</a>  </p>
      <p>Bond VC, Powell M, Huang MB, Ali S. USP 10,053,496. 08/21/18. Compositions and methods
         for exosome targeted expression. <a href="http://patft.uspto.gov/netahtml/PTO/srchnum.htm">http://patft.uspto.gov/netahtml/PTO/srchnum.htm</a></p>
   </publications>
   <awards><br></br>2015: Outstanding Mentor Award, Ph.D.<br></br><br></br>2014: Outstanding Mentors Award, MSCR Student Association <br></br><br></br>2012: Outstanding Mentors Award, PhD Student Association <br></br><br></br>2008: Faculty Appreciation Award, PhD Student Association</awards>
</profile>