{"id":4854,"date":"2015-06-27T15:40:00","date_gmt":"2015-06-27T19:40:00","guid":{"rendered":"https:\/\/www.med.unc.edu\/biochem\/directory\/kuhlman\/"},"modified":"2025-02-24T12:51:02","modified_gmt":"2025-02-24T17:51:02","slug":"kuhlman","status":"publish","type":"directory","link":"https:\/\/www.med.unc.edu\/biochem\/directory\/kuhlman\/","title":{"rendered":"Brian Kuhlman"},"content":{"rendered":"<p style=\"text-align: center\"><strong><span class=\"blue\"><em><span class=\"blue\"><em><strong>Oliver Smithies investigator, Professor <\/strong><\/em><\/span>of Biochemistry and Biophysics<\/em><br \/>\n<\/span><\/strong><span style=\"color: #333333\">Co-Director, <a class=\"external-link\" title=\"\" href=\"http:\/\/biophysics.unc.edu\" target=\"_self\" rel=\"noopener noreferrer\">UNC Molecular and Cellular Biophysics Program<\/a><\/span><strong><span class=\"blue\"><br \/>\n<\/span><\/strong><span class=\"discreet\">(PhD &#8211; State University of New York, Stony Brook) <strong><span class=\"blue\"><em><br \/>\n<\/em><\/span><\/strong><\/span><\/p>\n<p class=\" \" style=\"text-align: center\"><span class=\"btn btn-large btn-blue xxLargeFont normalSizeFont smallFont\" style=\"color: #ffff00\">ACCEPTING STUDENTS<\/span><span style=\"color: #333333\"><br \/>\n<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-10603 aligncenter\" src=\"https:\/\/www.med.unc.edu\/biochem\/wp-content\/uploads\/sites\/795\/2019\/08\/Faculty-OGE-Trained-mentor-badge-400dpi-for-website-300x181.png\" alt=\"Trained Faculty Mentor endorsed by Office of Graduate Ed UNC Chapel Hill\" width=\"300\" height=\"181\" srcset=\"https:\/\/www.med.unc.edu\/biochem\/wp-content\/uploads\/sites\/795\/2019\/08\/Faculty-OGE-Trained-mentor-badge-400dpi-for-website-300x181.png 300w, https:\/\/www.med.unc.edu\/biochem\/wp-content\/uploads\/sites\/795\/2019\/08\/Faculty-OGE-Trained-mentor-badge-400dpi-for-website-768x464.png 768w, https:\/\/www.med.unc.edu\/biochem\/wp-content\/uploads\/sites\/795\/2019\/08\/Faculty-OGE-Trained-mentor-badge-400dpi-for-website-1024x619.png 1024w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<div>\n<h3><span class=\"blue\">HONORS &amp; AWARDS<\/span><\/h3>\n<\/div>\n<div>\n<ul>\n<li>National Academy of Inventors Senior Member, 2025<\/li>\n<li>UNC Excellence in Basic Science Mentoring Award, 2020<\/li>\n<li>ASBMB DeLano Award for Computational Biosciences, 2019<\/li>\n<li>UNC Oliver Smithies Investigator, 2019<\/li>\n<li>W.M. Keck Foundation Distinguished Young Scholar in Medical Research, 2005-2010<\/li>\n<li>Searle Scholar, 2004-2007<\/li>\n<li>Beckman Young Investigator, 2004-2007<\/li>\n<li>AAAS Newcomb Cleveland Prize, 2004<\/li>\n<li>Foresight Institute Feynman Prize in Nanotechnology, 2004<\/li>\n<li>Alfred P. Sloan Fellow, 2004<\/li>\n<\/ul>\n<h3><span class=\"blue\">RESEARCH OVERVIEW<\/span><\/h3>\n<p><strong><i>Computational Protein Design \/ Protein-Protein Interactions \/ Antibodies \/ Structural Biology \/ Optogenetics \/ Rosetta<\/i><\/strong><\/p>\n<p><strong>What is protein design? <\/strong>Most ambitiously it is the creation of novel proteins to perform useful tasks. At a more modest level it might be identifying amino acid mutations that enhance protein stability, alter binding specificity, or increase solubility.<\/p>\n<p><strong>How do we design proteins? <\/strong>We are co-developers of a molecular modeling program called Rosetta that identifies low energy sequences for a target structure or interface. In essence, it is like solving a jigsaw puzzle. The pieces, in this case amino acids, must fit together so that there are no overlaps and little empty space. In addition, specific interactions such as hydrogen bonds must be satisfied.<\/p>\n<p><strong>What have we designed in the past? <\/strong>In the past we have used our program to enhance protein stabilities, design new protein structures, manipulate protein-protein interactions, and engineer protein switches.<\/p>\n<p><strong>What would we like to design in the future? <\/strong>Currently we are focusing on a variety of design goals including the design of light-activatable proteins, new strategies for creating therapeutic antibodies, the <em>de novo<\/em> design of protein structure.<\/p>\n<p class=\" \"><span class=\"blue\"><strong>What techniques do we use? <\/strong><\/span>Computer programming (primarily C++ and Python), molecular cloning, protein expression, biophysical analysis of protein-protein interactions (circular dichroism, isothermal titration calorimetry, surface plasmon resonance), directed evolution\/yeast display, X-ray crystallography, live cell imaging and microscopy<span class=\"blue\">.<br \/>\n<\/span><\/p>\n<h3><span class=\"blue\">RESEARCH TOPICS<\/span><\/h3>\n<p><strong><img decoding=\"async\" class=\"image-right\" src=\"resolveuid\/04b23eff43104d9d8657ea99ec15cb45\" \/><\/strong><strong>Optogenetics.<\/strong> Optogenetics describes the use of genetically encoded light-activatable proteins to control biological processes in living cells. Using a variety of protein engineering techniques, we have created a family of protein switches that can be used to control protein localization with light (see here for relevant papers). We have shown that these proteins can be used to activate GTPase signaling, control cell motility, and turn on gene transcription.<\/p>\n<p><strong><img decoding=\"async\" class=\"image-right\" src=\"resolveuid\/54792c61103e4ec3ad6b97eee5f08bec\" \/><\/strong><strong>Antibody engineering. <\/strong>Antibodies are invaluable reagents for biological research, and have emerged over the last 20 years as an important class of therapeutic. For the last five year, we have been engaged in a productive collaboration with Eli Lilly focused on the development of new strategies for engineering bispecific antibodies. Bispecific antibodies recognize two antigens simultaneously and can be used to enhance specificity to particular cell types as well as allow the co-localization of different cell types, for instance the recruitment of t-cells to tumor cells in order to fight cancer.<\/p>\n<p><strong><i>De novo<\/i><\/strong><strong> protein design. <\/strong>A long standing area of research in our laboratory is the development of computational methods for designing new protein structures from scratch. These projects allow us to probe the minimal determinants of protein structure, and provides the foundation for building new functional sites in proteins.<\/p>\n<p><strong>Protein interface design. <\/strong>Protein-protein interactions are central to all biological processes, and proteins with new binding properties can be used to manipulate biological pathways for applications in research and medicine. We have developed computational strategies for increasing protein-protein <span class=\"blue\"><strong><img decoding=\"async\" class=\"image-right\" src=\"resolveuid\/21d1f44f7d02428a8cd0c785b0a0e5fc\" \/><\/strong><\/span>binding affinities, manipulating binding specificities, and creating novel interactions. We have also explored approaches for effectively combining computational predictions with high throughput screening approaches like yeast display and phage display.<\/p>\n<p><span class=\"blue\"><strong>Rosetta methods development. <\/strong><\/span>Rosetta is a powerful modeling package with modules for protein structure prediction, docking and design. It is being developed by a consortium of over 30 universities and is continually being modified to improve performance and expand capabilities. Our laboratory has played an important role in parameterizing the current energy functions used by Rosetta, and we are now focused on enhanced strategies for parallel computing.<span class=\"blue\"><br \/>\n<\/span><\/p>\n<h3><span class=\"blue\">PUBLICATIONS<\/span><\/h3>\n<p><strong>2025<\/strong><\/p>\n<ul>\n<li>Dieckhaus H, Kuhlman B, (2025) Protein stability models fail to capture epistatic interactions of double point mutations.\u00a0<em>Protein Sci<\/em>\u00a0<strong>34(1)<\/strong>:e70003. PMCID: PMCID: PMC11659742<\/li>\n<li>Phan TTN, Hvasta MG, Thiono DJ, Shah RP, Prida Ajo G, Huang W-c, Lovell J, Tian S, de Silva AM, Kuhlman B. (2024) Multivalent administration of dengue E dimers on liposomes elicits type-specific neutralizing responses without immune interference. bioRxiv, https:\/\/doi.org\/10.1101\/2024.08.20.608851.<\/li>\n<li>Thiono DJ, Samaras D, Phan TTN, Zhu DR, Shah RP, Castillo I, Forsberg LJ, Premkumar L, Baric RS, Tian S, Kuhlman B, de Silva AM. (2024) Stabilized dengue virus 2 envelope subunit vaccine redirects the neutralizing antibody response to all E-domains.\u00a0bioRxiv, https:\/\/doi.org\/10.1101\/2024.07.18.604114.<\/li>\n<li>Yao Z, Kuhlman B. \u201cDesign of a Water-Soluble CD20 Antigen with Computational Epitope Scaffolding. (2024) bioRxiv, https:\/\/doi.org\/10.1101\/2024.12.05.627087.<\/li>\n<\/ul>\n<p><a href=\"http:\/\/www.ncbi.nlm.nih.gov\/sites\/myncbi\/brian.kuhlman.1\/bibliography\/43939489\/public\/?sort=date&amp;direction=ascending\">complete list of publications for Brian Kuhlman<\/a><\/p>\n<div>\n<hr \/>\n<\/div>\n<h3><span class=\"blue\">Lab Contact:<\/span><\/h3>\n<div>Lab Rooms: 3100D-F Genetic Medicine<\/div>\n<div>Lab Phone: 919-966-6781<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p><!-- description --> <\/p>\n<p class='lead'>Research: Protein Design, Protein Therapeutics, and Molecular Modeling<\/p>\n","protected":false},"featured_media":4855,"template":"","meta":{"_acf_changed":false,"layout":"","cellInformation":"","apiCallInformation":"","_links_to":"","_links_to_target":""},"class_list":["post-4854","directory","type-directory","status-publish","has-post-thumbnail","hentry","odd"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.8 - 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