yet. Even as they render the capacities and tendencies of complex systems calculable, the partially known haunts the liquid image.
We encounter an ominous spiked orb almost on a daily basis in reportage on theCOVID-19pandemic.ThosespikesattachwitheasetotheACE2receptors
ofhumanrespiratorycells,wearetold,enablingadeadlyviraltakeoverof
hostresources.Butwe’veheardthisstorybefore:SARS-CoV2doestores-piratorycellswhatHIVoncedidtoCD4cellsoftheimmunesystem.Anabiding
accompaniment to every pandemic is the visualization of virus
macro-molecules,theirapproachandentry,bloomandblastinhostcells.Despitethe
intensedesiretoseparateandisolatean“invisibleenemy,”wehavecometo
regard pathogenic particles in their vital relation to the hosts that they occupy.
Moving images based on structural data plunge us into wondrous voyages inwhichorbedbodiescircleandencountereachother(fig.1).Astheymorph
anddissolve,wewatchvirus-hostco-emergencesinthetwenty-firstcentury
“molecularfantastic.”1Operatingonasynthetic-biologiccontinuum,these
movingimagesarevitalmedia,whoseirreduciblevitalityismostevidentin makeslargevolumesofdatacohereasasingleinsight,aprocessthatstatis-ticianandartistEdwardTufte(2001)named“de-quantification.”2 Scientists
1 Withadvancedimagingtechnologies,inscientificedutainment,weareinthe
domain of the marvelous: a molecular fantastic of the same order as Akira Lippit’s
“opticalfantastic”inthefirsthalfofthe20th(triangulatingthedevelopmentofX-ray
technologies,thesplittingoftheatom,andpsychoanalysis,seeAtomic Light (Shadow Optics),MinnesotaUniversityPress,2005).Seemyaccountofthecellularagonin
“AnimatingUncommonLife:U.S.MilitaryMalariaFilms(1942-1945)inthePacificThe-ater,”inBeckman2014.
2 EdwardTufte,The Visual Display of Information(GraphicsPress,2001).
Of Liquid Images and Vital Flux 175
can keep abreast of structural data from multiple sources in contributing to editablemodelsoflivingsystems.Ontheother,thespeculativenatureof
theliquidimageisstrategicinkeepingupwithvitalflux.Onemightconsider
how genetic mutations that change instructions for protein assembly will impact the entry of viral biomolecules into host cellular receptors—an under-standingcriticaltodrugdesign.Forthe“bestunderstoodofanyorganism,”
asillustratorDavidGoodsellputsit,HIVclocksover90drugresistantgenetic
mutations.3 Scientists continue to visualize and simulate HIV “molecular dockingevents”athostcellularsitesthatenablethedesignofnewdrugs—
molecules which can sit in the docking site and block viral entry.4 Dynamic speculative images keep pace with evolving virus-human emergences in these molecular-cellular contexts.
[Figure1]Screenshotfrom“HIVLifeCycle”5
ThemediaticcaptureofHIV-1emergesattheintersectionofbasicscience
laboratories and creative media industries. While media histories starting fromthefirstcaptureofthetobaccomosaicvirusundertheelectronmicro-scopein1938revealashiftfrommorphologicalpreoccupationstodecoding
viralgenomesinthemid-twentiethcentury,biomolecularmodelsofvirus
3 StanfordUniversityHIVDrugResistanceDatabase(https://hivdb.stanford.edu/).
4 Scientificvisualizationsthatmodelcrowd-sourceddataplayacriticalroleinanti-viral strategies of epidemic mediation. The histories of SciVis are vast because they includematerialpracticesobtainingacrosscomputergraphics,biosciencelaboratory
techniques,andvirtualart.Idiscusstheirconjugationfurtherinmycurrentbook
project,The Virus Touch: Theorizing Epidemic Mediation.
5 Fortheanimation,seehttps://vimeo.com/260291601. This was made collaboratively with the Department of Biochemistry at the University at Utah and the CHEETAH consortium (https://biochem.web.utah.edu/iwasa/projects/HIV.html).JanetIwasa(AnimationLab),
whosescientificanimationsIhaveexploredelsewhere,headedtheprojectwithdata
sourcedfromresearchersglobally.See,Ghosh2016.
176 Pandemic Media
macromolecules remain critical to integrative research.6 No doubt the push arrives with the turn to complex systems thinking in the life sciences that made computation central to the study of living organisms. In attempting to understandtheeffectsofvitalprocessesatonescale(e.g.biochemicalcellular
reactions)onanother(e.g.foldingofproteinmolecules),scientistsofdifferent
clothincreasinglysharestructuraldataandtestcompetinghypotheses,com-municate and educate on new media platforms such as (Maxon’s) Cinema 4Dor(Autodesk’s)Maya.The“molecularmovies,”astheyaredubbed,are
robustcollaborationsbetweenacademicresearchers,biotechcorporations,
and digital animators.7Makingtheunseenvisible,astheSciVismantragoes,
moving images integrate structural data and simulate possible molecular events in this post-cinematic context. With new data inputs come new possibilities.
Inliquidimages,“life”asvitalprocessappearsas“lifeitself.”Asshorthand,
“lifeitself”referstothemediaticappearance of vital processes.8 Life “emerges with”matter:bodilymedialikebloodorrespiratorymucosasustainthevirus.
Technical-aesthetic mediation detects and composes the interactions of viral particlesinbodilyfluidsasthenumericdistributionofx copies in y milliliter blood(àlatheviralloadtest).SarahKemberandJohannaZylinska(2010)name
research on identifying viruses began in earnest. The focus on virus morphologies soongavewaytotheromancewithgenomiccodesinthemid-20th century as molecular biologistsdrilleddowntogenomicfingerprintsofvirusesinhostDNA.Thelatter
remainsthebedrockofvirologicalresearch,evenas,stilllaterinthe20thcentury,the
onus fell on integrating research with the rise of systems biology.
7 ThemantraisassociatedwithSciVispracticeswhichbeginstocommerciallycohere
in the late eighties (the precedents in molecular graphics go back much further). The firstSciViscongregation(theVisualizationinScientificComputingConference),in
1987,broughttogetherindustry,academics,andgovernmentofficials.Thus,beganthe
industrial enterprise of new media platforms that allowed scientists and animators to produce images based on experimental data necessary for designing source materials
readying them for other interventions such as gene-splicing or drug therapy.
9 Forthemultisensorydimensionofbuildingproteinmacromolecules,oneofthebest
studiesisNatashaMyers’(2015)ethnographyofproteincrystallography.Myerstraces
Of Liquid Images and Vital Flux 177
The point is better made with brief illustration: I focus on the making of HIV macromolecules at the Center for Computational Structural Biology (formerly,MolecularGraphicsLab)attheScrippsResearchInstitute,Univer-sityofCalifornia,SanDiego.Itschiefbiologist,ArthurOlson,wasapioneer
in the computer graphics foundational to molecular visualizations. Founded in1981,the“OlsonLab”(asitisnicknamed)sourcesitsdatafrommolecular
biologists(studyinggenetranscriptions),biochemists(studyingchemical
interactions),andstructuralbiologists(studyingproteinassemblies)tobuild
integrative crowd-sourced models which allow researchers to move beyond their silos of expertise.10Untilnow,thelabhasmadesixmodelsoftheHIV-1
macromolecule on media platforms so that researchers can manually move moleculesaround,watchforfolds,accelerateordeceleratemotion.Whilethe
game industry’s VR platforms provide inspiration for analyzing biomolecular structuresin3-D,sophisticatedtoolkitsspecificallytailoredforbiological
researcharenowavailable;someofthesehavebeendevelopedattheOlson
Lab.11Abiology-specificextensionofthebetter-knownAutoPACKisasuiteof
programscalledcellPACK,whichwasdevelopedincollaborationwithmed-ical-illustrator-turned-software-designerGrahamJohnson(MesoscopeLab,
UniversityofCalifornia,SanFrancisco).12 Structural biologist and illustrator DavidGoodsell’slegendary“zoomable”watercolors,whichmagnifiedcellular
structuresintotheirmolecularcomponents,arethemethodologicalandaes-theticbasesforbuildingunifiedhybridmodelsoncellPACK(fig.2a).13
the haptic and kinesthetic qualities of modeling proteins to argue for a sensuous engagementwithscientificmolecularstructures.
10 Arthur Olson has been envisioning HIV from the start of the epidemic in the United States.StudyingthestructuraldimensionsofHIV,theOlsonLab’s“AIDS-RelatedStruc-turalBiologyProgram”isanNIH-fundedoperation.Theteamatthelabincludesarange
of scientists from David Goodsell (on the technical-aesthetic end) to Stefano Forli (on the biotechindustryend).Thelabdevelopedatleastonethousandstructuresofprotease,
one of the three important HIV enzymes in the viral replication cycle. Research on HIV enzymebiostructureshaseverythingtodowiththelife-savingproteaseinhibitors,
placingtheOlsonLabsquarelywithinongoingeffortstodeveloppharmacological
solutionsto“managedHIV”(asitisnowcalled).
11 Intheareaofsoftwareprograms,thelab’ssuccessesaremany.“Autodock,”aprogram
forbiomolecularstructureanalysis,hasbeenadoptedbyfourthousandlaboratoriesall
over the world.
12 cellPACK was developed at the Olson Lab (with Ludovic Antin) while Johnson was finishinghispost-graduatework.Theopen-sourceprogramintegratesstructuralbiology
andsystemsbiologydatawithpackingalgorithmstoassemblecomprehensive3D
modelsofcell-scalestructuresinmoleculardetail.
13 DavidGoodsellisacentralfigurewhoiswellknownforhiswatercolorillustrations
basedonrealdatasourcesandmagnificationspecifications;theseareavailableonthe
ProteinDataBank.Goodsellhasnotonlyledonthescientificfront,buthisbooks, The Machinery of Life(1993)andAtomic Evidence(2016),arewidelyconsideredexemplarsof
sciencecommunication.Basedonhisaestheticprotocols,theOlsonLabhasproduced
asmanyas6HIV-1modelstodate(HIV-11.2,1.3…),eachmanuallycuratedwithwidely
sourced data.
178 Pandemic Media
[Figure2a–b]WatercolorofHIVinBloodPlasma,1999;HIV-in-BloodPlasmaVisualization,2015
The idea is to combine data from all branches of biology into a compre-hensivemesoscalemodelrangingfrom0.1micronto10nanometers.“Artistic
depictionsofcellularenvironments”builtonthecellPACKsuitecanintegrate
datafromultrastructural(lightandelectronmicroscopy),infrastructural
atomic(x-raycrystallographyandNMRspectroscopy),andbiochemical
(forconcentrationsandinteractions)sources(Johnsonetal.2015,85-91).
“Ingredients”fromthesedatasourcesproducescientific“recipes”(asthelab’s
extendedcookingmetaphorruns)forvariouspartsofthemodel.Fig.2bisan
image,HIV-in-Blood Plasma,madeupofsevendifferentrecipes(eachwitha
differentcolorcoding)thatareunifiedintoasinglemodel.Endlessupdatesto
the“editablemodelofHIV”becomepossibleintheseplastic,malleableliquid
images.TheOlsonLab’sHIV-1ultrastructure(theHIVenvelope)functionsas
thepolyhedral“mesh”orEuclidean“statespace”(addingtimetogeometric
coordinates)forpackingingredients(DeLanda2011).Thisisaccomplishedby
cellPACK’svirtuoso“packingalgorithms”thatdeterminehowthemeshisfilled
outtoproduceascalableimage(seefig.3).
Of Liquid Images and Vital Flux 179
[Figure3]PackingtheHIV-1mesh
Such a drive toward consistent precision in modelling biomolecular structures enablesthestudyof“activesites”oncellularsurfacesthatdrugtherapies
targettoblockthesuccessful“docking”ofHIV.StefanoForli,whoisthebio-techinterfaceatthelab,explainedhowanimating3-Dmodelsonnewmedia
platformsnotonlyprovidedtheopportunitytocircle,view,andanalyze
cellularstructures,butitalsoenabledcalculatingthedensities,forces,and
propensities of molecules as they interacted with each other. Real-time video-trackingallowedformovingmoleculesaround,acceleratingordecelerating
molecularmotion.AsthemoleculesvibratedinBrownianmotion,Olson
noted,scientistscouldbetterunderstandtheelectrostaticcomplementarity
and hydrogen bonding that forms molecular structures. They could zoom into specificsitesofstructuraluncertaintyandthenouttothebiggerpicture—the
HIV-1viralcapsidintheextracellularenvironment.
Thisexampleofliquidimagesdisclosestheirinfinitemalleability.Tobesure,
these“technicalimages,”torecallVilémFlusser(1985),concretizinga“universe
ofparticlesmovingtowarddissipation,”areasplasticasareall digital images.
Eachimageliquidatesandreconfigurestheprevioustrace.Andyet,thepoint
of the constant update is to keep up with high volumes of incoming data:
theOlsonLab’sreleaseofHIV1.6demonstratedthepossibilityofintegrating
crowd-sourced structural data at speeds commensurate with the fast pace of
180 Pandemic Media
research(Johnsonetal.2014,23-44).Further,whenanimated,scientistswere
able to experiment with multiple outcomes for the molecules in motion—
colliding,adhering,separating.Suchdynamismiscriticaltosimulatingthe
changefulinteractivityofparasiticrelations.Asobligateparasites,bitsof
nucleicacidwithaproteincoatandwithoutcellwalls,weknowthatviruses
“comealive”assecondaryorganismsalwaysinvitalrelationtoahost;they
need host resources to replicate.14 But this biological partnership is con-stantly negotiated as virus-host vital relations continue to emerge.15 Computer animationscansimulatetheprocessualitiesofemergences,predictingarange
of probable outcomes for the form and evolution of vital relations.
Investigatingsimulationsoflivingsystems,ManuelDeLanda(2011)examines
the computational rendering of biologic “possibilityspaces”—thespaceof
genes,thespaceofstructuralproteins,thespaceofspatialstructures—into
synthetic possibilityspaces.Theefficacyofthescalable liquid image lies in rendering biological possibilities as calculable mathematical probabilities.
Inthisenrichedmechanisticaccountoflife,DeLandaasks:What“individual
singularities”ariseininteractionsbetweenagentswithinapossibilityspace?
Definingindividualsingularitiesasnew properties,DeLandaarguesthat
hydrogenandoxygenproducealiquidstatemorethanthesumofitsparts,a
state whose properties (such as the temperature at which water boils) are dis-tinct from the two gaseous entities. Secondary mutations of HIV that evolve as
14 Eversinceitsdiscoveryinthelate19thcentury,thevirushasalwaysbeenaborder
object,inthesensethatitlacksanimportantdefinitivefeatureoflivingorganisms—the
as opposed to a facultative parasite that can live independently but becomes parasite undercertainconditions.Theviruscanonlylivewithinhosts.Itliterally“comesalive”
from dormant crystalline states when it senses a host.
15 Oneoftheforemostscholarsofparasitism,AngelaDouglascharacterizessymbiosisas
a derived state: a gradual evolutionary transition from antagonism (including virulent pathogenesis)tomutuallybeneficialrelationsincludingastable,managedpartitioning
of resources.Onepartner,usuallythehost,takescontrolofresourcedistributionover
time,imposingsanctionsandcontrollingtransmissionsforbothpartners,evenasboth
organismsdevelopnovelcapacities(alateral,nothereditary,transferofproperties)in
order to live with the perturbations that the other generates. Symbiosis-at-risk is one steponaspectrumofrelationsbetweenparasitesandhosts;andsomerelationships
(e.g. human-Ebola) never move past that point. Symbiotic relations are those that are mutuallybeneficialtotheparticipantsforthemajordurationoftheirlifetime.Thisdoes
notmeanthatparasitismisnotsymbiotic,butthatpathogenicparasitismisnot.Less
virulentparasitesareataselectiveadvantageinthisregard,sincetheydonotdeplete
theresourcesofthehost.Wecan“livewith”virulentpathogenslikeHIVonlywiththe
technologicalmediationofdrugtherapies.See,AngelaDouglas,The Symbiotic Habit (PrincetonUP,2010),Symbiotic Interaction(1994),andThe Biology of Symbiosis(1987).
Of Liquid Images and Vital Flux 181
drug resistance are examples of such individual singularities: these properties emergeatnegotiationsbetweenhostresources,viralparticles,andchemical
drugmolecules.Whilesuchnewpropertiescanbedecodedanddocumented,
what remains speculative are the capacities and tendencies that come into play within living systems. Enter liquid images: the attempt to predict outcomes of new individual singularities arising in cellular environments.
Asanimagecomposedatonescaleliquidatestoreassembleintoanother,
perhapslarger,whole,orviceversa,liquidimagesnotonlypresentvariable
trajectories but they also predict what is not yet known. They are crucial sites forcreativeactualizationsofscientifichypothesesbasedonmathematical
possibilities. Whether those hypotheses concern envisioning the capacities andtendenciesofcomplexsystems,ortrackingevolvingchangesinnew
after years of study. Even though HIV is relatively simple in its composition (madeofjusteightstructuralproteins),the“HIVtrimer”wasonthe“most
wanted”listofproteinmacromoleculesuntil2013,whenthescientificcom-munitycouldagreeonitsdefinitivecrystallinestructure.Theliquidimageis
an object lesson in patience.
WewillhavetoinhabitthemolecularfantasticofSARS-Cov2forthefore-seeablefuture,watchingasthisincreasinglyfamiliarorbcirclesandenters
itsnewhosts,leavingcellularruininitswake.Theliquidimageisalwaysat
alagforvitalfluxcontinuestoexceedallsynthetictranscription.Delving
deeper,movingfaster,thesespeculativeimagesremaininhotpursuitofever-emergent virus-host vital relations.
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