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  <title><![CDATA[CANCELED: Sustaining Life with Genes and Proteins Designed ‘From Scratch’]]></title>
  <body><![CDATA[<p>THIS SEMINAR WAS CANCELED DUE TO WEATHER.</p>

<p><strong>Michael Hecht, </strong><strong>Ph.D</strong><strong>.<br />
Department of Chemistry<br />
Princeton University</strong></p>

<p><strong>ABSTRACT</strong><br />
A key goal of synthetic biology is to design novel proteins that fold and function <em>in vivo.&nbsp; </em>A particularly challenging objective would be to produce non-natural proteins that don&rsquo;t merely generate interesting phenotypes, but which actually provide essential functions necessary for the growth of living cells. Successful design of such life-sustaining proteins would represent a step toward constructing &ldquo;artificial proteomes&rdquo; of non-natural sequences. &nbsp;In initial work toward this goal, we designed large libraries of novel proteins encoded by millions of synthetic genes.&nbsp; Many of these new proteins fold into stable 3-dimensional structures; and many bind biologically relevant metals, metabolites, and cofactors. &nbsp;Several of the novel proteins function <em>in vivo</em> providing essential activities necessary to sustain the growth of <em>E. coli</em> cells. In some cases, these novel proteins rewire gene regulation and alter the expression of endogenous genes.&nbsp; In other cases, the novel protein sustains cell growth by functioning as <em>bona fide</em> enzyme that catalyzes an essential biochemical reaction. These results suggest that (i) the molecular toolkit of life need not be limited to sequences that already exist in nature, and &nbsp;(ii) artificial genomes and proteomes might be built from non-natural sequences.</p>

<p><a href="http://chemlabs.princeton.edu/hecht/">About the Hecht Lab</a></p>

<p>Host: Frank Rosenzweig</p>
]]></body>
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      <value><![CDATA[<p><a href="mailto:jasmine.martin@biosci.gatech.edu">Jasmine Martin</a></p>
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