Spoznajte ikonu hudobného sveta

Napísal Albatros Media, Lindeni 20. apríl 2019

David Bowie bol viac ako spevák, viac než umelec. Jeho vplyv na modernú popkultúru je nezmazateľný. Práve o ňom je nádherná kniha Bowie: Ilustrovaný životopis od španielskej autorsko-ilustrátorskej dvojice Fran Ruiz – Mariá Hesseová, ktorá práve vyšla vo vydavateľstve Lindeni. 

Vďaka nej budete mať pocit, že príbeh o životnej dráhe Bowieho počúvate priamo z jeho úst. Spoznajte muža mnohých tvárí, kontroverznú ikonu hudobného sveta aj jeho alter ego Ziggyho Stardusta.

Beletrizovaná biografia s iluzórnymi ilustráciami a surrealistickými motívmi odráža to, čo Bowie celý svoj život predstavoval – zmes obrovského talentu, nápaditého štýlu aj krehkej duše. A tak poňali aj knihu autor Fran Ruiz a ilustrátorka María Hesseová.„Bowie bol majstrom afektovaného správania, zahmlievania a tajnostkárstva. Aby sme vám porozprávali jeho príbeh, rozhodli sme sa zachovať rovnaký prístup. Prostredníctvom svojho diela nás náš hrdina naučil, že ukazovať veci z jediného uhla pohľadu, nech by bol sebaúprimnejší, môže byť vo výsledku falošnejšie, ako ponúkať roztrieštenú a nejednoznačnú podobu,“vysvetľujú hneď v úvode knihy, ako vznikala. „Nielen kvôli tomu, ale aj preto, že si uvedomujeme, že každá biografia je napokon do istej miery fikciou, sme sa rozhodli, že reálne okamihy Bowieho života zmiešame s fantazijnými prvkami...“

Kniha na 168 stranách popisuje zásadné aj menej známe okamihy života umeleckého mága, ktorý skonal na rakovinu v januári 2016. Dva dni pred smrťou, na svoje 69. narodeniny stihol ešte vydať svoj dvadsiaty piaty štúdiový album Blackstar, o ktorého nahrávaní nemal takmer nikto ani potuchy. Na zem, podľa svojich slov, prišiel ako hviezdny prach a odišiel, už podľa fanúšikov aj kritikov, ako legenda. „Som kapitán Tom. Ziggy Stardust. The Thin White Duke. Som mimozemšťan. Kráľ škriatkov. Som sloním mužom. Umierajúcim, ktorý nemôže umrieť. Som bratom toho, ktorý odvráva. Som Lazarom. Človekom, ktorý na svojich bedrách nesie veľkú čiernu hviezdu. Ja sám som tou čiernou hviezdou. Som všetko, čo si nevieš predstaviť,“ začína sa tajomne jeho ilustrovaný životopis. Stačí sa už len pustiť do čítania a vnímať, kto vlastne David Bowie bol.

Aj keď nevedno, či vám to sám spevák umožní:„Hneď, ako sa rozhodneš rozpoznať, čo sa schováva za mojím tieňom, budem už znovu prevtelený.“

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    The beads had been washed with pre-RC buffer and the proteins nonetheless
    sure to DNA were eluted by DNase I. The eluate was analysed by SDS-PAGE stained with
    silver or coomassie blue. The SDS-PAGE outcomes had been used
    to discover out DH-DDK interaction. In contrast to a Cdc7 kinase inhibitor,
    this mode of inhibition could permit increased specificity for
    the inhibition of helicase activation. To our surprise, within the MD-(ATPγS) structure we observed an ATPγS molecule bound to the
    Oligonucleotide/Oligosaccharide-Binding (OB)-fold interface of Mcm2/6, a non-canonical nucleotide-binding web site (Supplementary Fig. 11a).

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    The data also signifies that the flexibleness of the Mcm4 tail alone may
    not be sufficient for substrate binding and provides a model for target selection of DDK atypical websites.

    The MD-(ATPγS) structure can readily clarify how Cdc7 can attain the Mcm4 N-terminal extension and phosphorylate it, because the Mcm
    tail is in direct proximity to the kinase. Nevertheless,
    DDK also phosphorylates Mcm2 and Mcm6, that are distant from the observed binding web site.
    We questioned whether or not alternative constructions may exist
    and therefore screened ATP analogues for various conformational states (Supplementary Fig. 1d).
    We discovered that within the presence of ADP-BeF3,
    DDK adopts two totally different conformations on the DH, specifically MD-(ADP-BeF3) state I and MD-(ADP-BeF3) swiveled state,
    in a ~70/30 distribution, respectively (Fig. 6b, c; Supplementary Fig. 8).

    The calculated weight might sound deceptively light, but
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    This contrasts the end result seen with the DNA sure DH construction, which had no nucleotide at the Mcm7/4
    and Mcm4/6 interfaces and ADP on the remaining nucleotide-binding sites.

    This contrasts earlier biochemical observations46, which didn't detect significant ADP release, doubtlessly because
    of the longer incubation time or the addition of DDK in our experiments.
    Out of the three MD complexes, state III was resolved to the best imply decision of three.1 Å,
    with DDK having a neighborhood decision of three.5 Å (Fig. 
    1d and Supplementary Fig. 3). We resolved density for 87% of Cdc7, including all conserved kinase motifs,
    41% of Dbf4, together with the conserved N,
    M and C motifs and 72% of MCM2-7 (Fig. 1c–e and
    Supplementary Fig. 4).
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    Just Lately, it was proven that the unstructured tail of Mcm2 is also
    required for DDK recruitment14,15, but the mechanism is still unclear.

    As such we propose that the unstructured tail acts as an preliminary contact, which consequently becomes complemented or replaced by the Mcm2-HBRCT-Dbf4 interaction.
    This dual recruitment mechanism can doubtlessly explain why deletion of the Dbf4
    HBRCT domain is lethal in embryonic mouse cells60 and never in yeast44.
    A–d Three different structural states (I-III) derived
    from the same MD-(ATPγS) cryo-EM data set. A Cryo-EM 3D auto-refined map (see Methods) of MD-(ATPγS) state I.

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