Ann Burlein,
"The Molecular Body and the Christian Secular"
(page 4 of 7)
Section Two
Molecular Shifts of Fate and the Romance of
Gender: Desire and Duty in the Molecular Body
It can at first seem counter-intuitive to claim that genetics
positions us vis-à-vis the biological body through different relations
than the shame and death that characterized the modern clinic.
Physicians speak of genetic errors as 'lesions,' much as doctors in the
modern clinic looked for lesions on tissues. The gene has been
stubbornly imagined in scriptural terms (although scientists
disconfirmed the accuracy of images like 'information,' 'language,'
'code,' and 'text' in the
1950s).[49][50]
The dream of mapping the dark
continent of the body's submicroscopic interiors was crucial to enabling
the massive computer sequencing required for the HGP to be cast as the
next step in American Manifest Destiny and thus to be funded by
Congress.[51]
Yet these lines of continuity unfold within a different horizon. The
project of molecular biology was never imagined as tearing aside the
visible body to uncover the mute violence devouring us in our inner
darkness. Idealizing molecular biology as the science of life that could
resurrect something good out of WWII helped crystallize a new origin
story for a genetics anxious to reject eugenics. Explicitly
distinguished from nuclear physics (epitomized by Oppenheimer quoting
Krishna: "I have become death, the destroyer of worlds"), molecular
biology was promoted as an essential tool in the Cold War arsenal that
could provide solutions to the dangers spawned by atomic radiation and
later by the population bomb.[52]
More generally, this dream of life and its boundless productivity
also animated the post-Fordist economy more generally. The thought was
that unleashing the creativity of scientific minds could enable Western
societies to escape death and waste—the very limits of industrial
production. Cooper points to economists in the 1970s who began to argue
that Fordist economies would necessarily decline due to finite resources
and aging populations. At the same time, big pharma began to face the
end of its patents on the miracle drugs of the mid-century, while
chemical industries began to face the eclipse of the Green Revolution in
agriculture. In response to this conjuncture, Post-Fordist regimes
emerged. Tracing a "tight institutional alliance" between "epistemic,
experimental, and commercial modes of speculation," Cooper contends that
the model for these new or post-Fordist modes of accumulation is the
generation of surplus value from life's capacity for future
capacity.[53]
She writes: "the biotechnological solution to economic
limits seems to encapsulate the speculative euphoria of revalorization
at the most intimate of material
levels."[54] Such regimes promise to
render even debt productive, both the colossal debt of the United States
as well as the expanded sense of debt to life that characterizes much
public discourse around the genome.[55]
While degeneration and disease remain a concern in molecular
medicine, the wear and tear of tissues is no longer taken as the last
word on organic life. Nor is in-depth knowledge of a thing's history
taken to constitute what it means to know. No longer the amoral nature
of animals, biological life becomes a matter of forces on whose surface
effects calculated transformations can take hold, re-working even time.
Hence knowledge that focuses on the hopes and risks of biological
control dreams less of prevention (although fears are invoked) and more
of pre-emptive optimization. Knowledge-power relations here aim less to
discipline than to arouse and to facilitate, to allow natural processes
to do their thing on one level of development, so as to produce a
desired effect on another level of
development.[56] Today 'we' dream
that reading the digital Book of Life will enable us to tap the forces
of life directly.
Consider how private umbilical cord banks use the fact that different
parts of the body wear out at different rates to promote themselves as
biological insurance: "You miss the chance if you decide to throw out
the cord blood," says one lab
director.[57] Here 'waste' generates
value. According to Waldby and Mitchell, private cord blood accounts
provide a new relation to tissues: neither gifts (blood banks) nor
commodities but family property that pre-empts claims by others even as
it doubles biological time. The account holder's body ages while the
preserved tissue retains the capacity to recreate the blood system
should need
arise.[58][59]
One does not extract value from this kind of family property by
learning to relate to oneself as a being "inhabited by a deep internal
space shaped by biography and experience, the source of our
individuality and the locus of our
discontents."[60] Rather than hinging
on confession, producing value out of life's capacity for future
capacity hinges on manipulating the molecular memories that link soul to
body through a fate that 'flattens' identity into temporal
networks.[61]
This flattening authorizes different expectations (than
seeing through the visible body into its invisible depths). The
perception that biological life and human control are inextricable
generates the expectation that 'we' can touch life's nascent forces of
(re)generation by means of targeted interventions so 'small' they become
'smart.' 'We' dream not merely of using biology as raw material, but of
directly shaping the biological body's capacity for future capacity.
The hopes and risks of smart touch are grafted onto the flatness of
molecular mechanisms most often through a rhetoric of impersonality that
re-animates the scientific secular by updating Foucault's 'speaker's
benefit.' Consider its articulation around race. If the twentieth
century was the century of the gene[62]
and the color line[63],
twenty-first century science asserts the hope of 'biological control' by
promising that accessing molecular pathways will free us from the social
shame of racial disparities (now deemed merely
cultural).[64] The hope
here is that medical professionals will see sickle cell disease, for
instance, as a matter of genetic mis-codings and thus resist any racial
stereotypes that arise when confronted with young African-American men
in an emergency room asking for narcotics. Rather than refusing to treat
'the whole patient,' evidence-based medicine claims that focusing solely
on molecules can short-circuit prejudices. A similar hope undergirds
support for medications like BiDil (the first heart medicine marketed to
African-Americans). Supporters contend that we can circumvent the
cultural causes of racial disparities in health care through protocols
that use race as proxy, or (even better) that prescribe BiDil not
because a patient 'looks black,' but because their blood exhibits lower
levels of nitric oxide (which BiDil raises; African-Americans as a
group, although not every individual African-American, have less nitric
oxide in their blood).[65][66]
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