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- From: sidles@stein.u.washington.edu (John Sidles)
- Newsgroups: sci.physics
- Subject: Re: Compelling Mysteries (II)
- Keywords: compelling, mysteries, partridges and pear trees
- Message-ID: <1992Nov11.051323.25125@u.washington.edu>
- Date: 11 Nov 92 05:13:23 GMT
- Article-I.D.: u.1992Nov11.051323.25125
- References: <2191@eagle.ukc.ac.uk> <1992Nov10.194812.101645@watson.ibm.com> <1992Nov10.195415.124349@watson.ibm.com>
- Sender: sidles@u.washington.edu
- Organization: University of Washington, Seattle
- Lines: 108
-
- >|> |> > Several people have complained lately about the subject matter
- >|> |> > around this neck of the woods, so I wonder if some of those people
- >|> |> > will oblige me by posting what they believe to be compelling
- >|> |> > mysteries or pressing problems in their particular field.
-
- Dear "sci.physics" folks...
-
- Here is a medical perspective on what constitutes a "pressing
- problem" in physics. It concludes with a challenge to the
- collective theoretical, experimental, and inventive powers of
- the sci.physics community.
-
- I am an associate professor of orthopaedics. In our clinic,
- patients frequently present with problems that are beyond the
- reach of present orthopaedic practice. For example, two of
- the most vexing problems we face in orthopaedics are aging
- and HIV infection. Neither is susceptible to surgical treatment.
- But neither do we know very much about the molecular basis of
- these disorders.
-
- With regard to aging, one can't prepare pure samples of aged
- collagen for x-ray or NMR structural analysis, because aged
- collagens are heterogenous. So at the molecular level, we
- have limited understanding of the structural pathogenesis of,
- for example, osteoarthritis.
-
- In our clinical practice, we are limited to "cut and replace"
- treatment of severely osteoarthritic joints, using plastic
- and steel artificial joints. It would be much better if we
- knew how to prevent, and how to cure, osteoarthritic degeneration.
- There is not much hope of achieving this until we learn more
- about whatis going on at the molecular level.
-
- Regarding HIV infection, the orthopaedic surgeons in our
- department are committed to treating every patient who comes
- in the door. As a regional trauma center we treat many urban
- trauma patients who have a high prevalence of HIV infection.
- So our surgeons are at substantial risk for HIV exposure, and
- minimizing this risk requires stringent precautionary measures.
- This makes orthopaedic practice much more stressful... and
- this is not a trivial concern, as it becomes difficult to
- recruit surgeons willing to treat these patients.
-
- Molecular biologists have acquired fairly complete knowledge
- of the HIV genome, but not much structural information about
- the proteins it encodes. This makes rational design of
- effective treatments very difficult and slow. To the extent
- that better instruments for obtaining molecular structure
- information might speed medical research, everyone would
- benefit.
-
- Some non-biologists don't appreciate that presently there are
- no good methods for nondestructive, single-copy molecular
- structure determination. Yet from a clinical perspective,
- this lack severely impedes medical research. It is as though
- scientists had to study cell structure without using microscopy.
- Instead, scientists would learn about cells by homogenizing,
- filtering, and centrifuging them. After much work, they might
- determine that cells are surrounded by membranes, and contain
- nuclei carrying genetic information, etc. Biomedical researchers
- would not feel handicapped by the lack of microscopy, rather
- they would compete for access to the newest and most ingenious
- filtering devices. In this hypothetical world, it would not
- be readily apparent that instrument technology was a crucial
- medical/scientific issue.
-
- Hopefully, the next generation of molecular biologists will
- routinely, quickly, and easily obtain images showing the full
- three-dimensional structure of the molecules they are studying,
- in situ, with all their ligands, cross-links, and glycosylation
- in place. This would substantially accelerate the development
- of effective treatments for presently intractable disorders.
-
- The challenge posed to the collective theoretical, experimental,
- and inventive powers of "sci.physics" is this: design a
- molecular microscope with the above-named capabilities.
-
- Three concluding comments...
-
- (1) One stimulus for posting this note is Leo Kadanov's
- too-downbeat editorial in this month's Physics Today... you
- young folks should keep in mind that there still remain many
- "compelling mysteries and pressing problems" where physicists
- can make contributions that are both aesthetically pleasing
- and socially useful.
-
- (2) If your ideas are good,then write them up and submit them
- for publication. If your ideas are too half-baked for
- publication, then submit them to the net. But please don't
- send your ideas to me... I won't read them. Everyone is better
- off if you take the trouble to write things up clearly,
- referencing the relevant literature, and submit for publication.
-
- (3) To avoid being disingenuous, I have to state that my
- colleagues and I have published in this area, most recently
- in Rev. Sci. Instrum. 63(8) 3881-3899 (1992). But my strong
- recommendation is to think about the problem independently...
- surely physicists can come up with better ideas than an
- orthopaedist can!
-
- ---------------------------------------------------------------------
- John Sidles, Ph.D. email: sidles@u.washington.edu
- Associate Professor phone: (206) 543-3690
- Department of Orthopaedics RK-10 FAX: (206) 685-3139
- School of Medicine
- University of Washington
- Seattle WA 98195
- ---------------------------------------------------------------------
-