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Beyond the Molecular Frontier: Challenges for Chemistry and Chemical Engineering (2003)
Board on Chemical Sciences and Technology (BCST)

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Beyond the Molecular Frontier: Challenges for Chemistry and Chemical Engineering

the three-dimensional chemical structure of the multimolecular photosynthetic reaction center, for which Johann Deisenhofer, Robert Huber, and Hartmut Michel received the Nobel prize in 1988. New advances in imaging will be needed to delineate these and still larger macromolecular assemblies at atomic resolution. These structural pictures provide a critical foundation for understanding how they function. But how do these machines assemble? Are they remarkable examples of spontaneous supramolecular assembly or are they guided in some way in coming together? How do the parts of these assemblies function in concert? Are macromolecular assemblies of such complexity required to carry out these functions? Indeed, can we next begin to design novel macromolecular machines to carry out new, still more complex functions? The construction and assembly of such machines would represent the first step in compartmentalizing chemical reactions. As such, it would represent the very first steps in a tremendous challenge to the chemist and chemical engineer, the design of a synthetic cell.

Sequencing the Human Genome

The year 2000 marked the completion of the Human Genome Project’s primary goal. Through intensive efforts of both private and public agencies, the sequence for the three billion base pairs that encodes the instructions for being human has now been determined.5 As a result of the Human Genome Project, we have determined the complete chemical structure, nucleotide by nucleotide, of the DNA within each of these chromosomes, the chemical structures that encode our lives. It is an extraordinary accomplishment in chemistry.

Completing this sequencing of the human genome could only be accomplished by building upon discoveries in chemistry made over the past 30 years. It was about 20 years ago that W. Gilbert and F. Sanger showed that small segments of DNA could be sequenced directly using chemical methods. About 10 years ago, instrumentation for automated sequencing was engineered. And building upon all the advances in biotechnology of the last decades, from oligonucleotide synthesis to the polymerase chain reaction and shot-gun sequencing, biochemists in the last 2 years have been able to increase the pace of analysis, so that full genomic maps can be deciphered in months.

In this post-genomic era, what can we expect? Mapping the human genome brings not only a high-resolution picture of the DNA within our

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J. D. McPherson, et al., Nature, 409, 934, 2001; J. C. Venter, et al., Science, 291, 1304, 2001.

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