Web address:
     http://www.sciencedaily.com/releases/2011/01/
     110106145311.htm   
Scientists Construct Synthetic Proteins That Sustain Life
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Michael Hecht, a professor of chemistry at Princeton University, has led a team 
of researchers who have for the first time constructed artificial proteins that 
enable the growth of living cells. The synthetic proteins were designed from 
scratch and expressed from artificial genes. He is holding samples of living 
bacteria containing the synthetic proteins. (Credit: Photo by Brian Wilson)

ScienceDaily (Jan. 7, 2011) — In a groundbreaking achievement that could help 
scientists "build" new biological systems, Princeton University scientists have 
constructed for the first time artificial proteins that enable the growth of 
living cells.

The team of researchers created genetic sequences never before seen in nature, 
and the scientists showed that they can produce substances that sustain life in 
cells almost as readily as proteins produced by nature's own toolkit.

"What we have here are molecular machines that function quite well within a 
living organism even though they were designed from scratch and expressed from 
artificial genes," said Michael Hecht, a professor of chemistry at Princeton, 
who led the research. "This tells us that the molecular parts kit for life need 
not be limited to parts -- genes and proteins -- that already exist in nature."

The work, Hecht said, represents a significant advance in synthetic biology, an 
emerging area of research in which scientists work to design and fabricate 
biological components and systems that do not already exist in the natural 
world. One of the field's goals is to develop an entirely artificial genome 
composed of unique patterns of chemicals.

"Our work suggests," Hecht said, "that the construction of artificial genomes 
capable of sustaining cell life may be within reach."

Nearly all previous work in synthetic biology has focused on reorganizing parts 
drawn from natural organisms. In contrast, Hecht said, the results described by 
the team show that biological functions can be provided by macromolecules that 
were not borrowed from nature, but designed in the laboratory.

Although scientists have shown previously that proteins can be designed to fold 
and, in some cases, catalyze reactions, the Princeton team's work represents a 
new frontier in creating these synthetic proteins.

The research, which Hecht conducted with three former Princeton students and a 
former postdoctoral fellow, is described in the online journal PLoS ONE, 
published by the Public Library of Science.

Hecht and the students in his lab study the relationship between biological 
processes on the molecular scale and processes at work on a larger magnitude. 
For example, he is studying how the errant folding of proteins in the brain can 
lead to Alzheimer's disease, and is involved in a search for compounds to 
thwart that process. In work that relates to the new paper, Hecht and his 
students also are interested in learning what processes drive the routine 
folding of proteins on a basic level -- as proteins need to fold in order to 
function -- and why certain key sequences have evolved to be central to 
existence.

Proteins are the workhorses of organisms, produced from instructions encoded 
into cellular DNA. The identity of any given protein is dictated by a unique 
sequence of 20 chemicals known as amino acids. If the different amino acids can 
be viewed as letters of an alphabet, each protein sequence constitutes its own 
unique "sentence."

And, if a protein is 100 amino acids long (most proteins are even longer), 
there are an astronomically large number of possibilities of different protein 
sequences, Hecht said. At the heart of his team's research was to question how 
there are only about 100,000 different proteins produced in the human body, 
when there is a potential for so many more. They wondered, are these particular 
proteins somehow special? Or might others work equally well, even though 
evolution has not yet had a chance to sample them?

Hecht and his research group set about to create artificial proteins encoded by 
genetic sequences not seen in nature. They produced about 1 million amino acid 
sequences that were designed to fold into stable three-dimensional structures.

"What I believe is most intriguing about our work is that the information 
encoded in these artificial genes is completely novel -- it does not come from, 
nor is it significantly related to, information encoded by natural genes, and 
yet the end result is a living, functional microbe," said Michael Fisher, a 
co-author of the paper who earned his Ph.D. at Princeton in 2010 and is now a 
postdoctoral fellow at the University of California-Berkeley. "It is perhaps 
analogous to taking a sentence, coming up with brand new words, testing if any 
of our new words can take the place of any of the original words in the 
sentence, and finding that in some cases, the sentence retains virtually the 
same meaning while incorporating brand new words."

Once the team had created this new library of artificial proteins, they 
inserted those proteins into various mutant strains of bacteria in which 
certain natural genes previously had been deleted. The deleted natural genes 
are required for survival under a given set of conditions, including a limited 
food supply. Under these harsh conditions, the mutant strains of bacteria died 
-- unless they acquired a life-sustaining novel protein from Hecht's 
collection. This was significant because formation of a bacterial colony under 
these selective conditions could occur only if a protein in the collection had 
the capacity to sustain the growth of living cells.

In a series of experiments exploring the role of differing proteins, the 
scientists showed that several different strains of bacteria that should have 
died were rescued by novel proteins designed in the laboratory. "These 
artificial proteins bear no relation to any known biological sequences, yet 
they sustained life," Hecht said.

Added Kara McKinley, also a co-author and a 2010 Princeton graduate who is now 
a Ph.D. student at the Massachusetts Institute of Technology: "This is an 
exciting result, because it shows that unnatural proteins can sustain a natural 
system, and that such proteins can be found at relatively high frequency in a 
library designed only for structure."

In addition to Hecht, Fisher and McKinley, other authors on the paper include 
Luke Bradley, a former postdoctoral fellow in Hecht's lab who is now an 
assistant professor at the University of Kentucky, and Sara Viola, a 2008 
Princeton graduate who is now a medical student at Columbia University.

The research was funded by the National Science Foundation.
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Story Source:

    The above story is reprinted (with editorial adaptations by ScienceDaily 
staff) from materials provided by Princeton University. The original article 
was written by Kitta MacPherson.

Journal Reference:

   1. Mark Isalan, Michael A. Fisher, Kara L. McKinley, Luke H. Bradley, Sara 
R. Viola, Michael H. Hecht. De Novo Designed Proteins from a Library of 
Artificial Sequences Function in Escherichia Coli and Enable Cell Growth. PLoS 
ONE, 2011; 6 (1): e15364 DOI: 10.1371/journal.pone.0015364

Need to cite this story in your essay, paper, or report? Use one of the 
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Princeton University (2011, January 7). Scientists construct synthetic proteins 
that sustain life. ScienceDaily. Retrieved January 8, 2011, from 
http://www.sciencedaily.com­ /releases/2011/01/110106145311.htm

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of 
ScienceDaily or its staff.




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