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Segmented flow generator for serial crystallography at the European X-ray free electron laser.

Austin EchelmeierJorvani Cruz VillarrealMarc MesserschmidtDaihyun KimJesse D CoeDarren ThifaultSabine BothaAna Egatz-GomezSahir GandhiGerrit BrehmChelsie E ConradDebra T HansenCaleb MadsenSasa BajtJ Domingo Meza-AguilarDominik OberthürMax O WiedornHolger FleckensteinDerek MendezJuraj KnoškaJose Manuel Martin-GarciaHao HuStella LisovaAschkan AllahgholiYaroslav GevorkovKartik AyyerSteve AplinHelen Mary GinnHeinz GraafsmaAndrew J MorganDominic GreiffenbergAlexander KlujevTorsten LaurusJennifer PoehlsenUlrich TrunkDavide MezzaBernd SchmittManuela KuhnRaimund FrommeJolanta Sztuk-DambietzNatascha RaabSteffen HaufAlessandro SilenziThomas MichelatChen XuCyril DanilevskiAndrea ParentiLeonce MekindaBritta WeinhausenGrant MillsPatrik VagovicYoonhee KimHenry J KirkwoodRichard BeanJohan BieleckiStephan SternKlaus GiewekemeyerAdam R RoundJoachim SchulzKaterina DörnerThomas D GrantValerio MarianiAnton BartyAdrian P MancusoUwe WeierstallJohn C H SpenceHenry N ChapmanNadia A ZatsepinPetra FrommeRichard A KirianAlexandra Ros
Published in: Nature communications (2020)
Serial femtosecond crystallography (SFX) with X-ray free electron lasers (XFELs) allows structure determination of membrane proteins and time-resolved crystallography. Common liquid sample delivery continuously jets the protein crystal suspension into the path of the XFEL, wasting a vast amount of sample due to the pulsed nature of all current XFEL sources. The European XFEL (EuXFEL) delivers femtosecond (fs) X-ray pulses in trains spaced 100 ms apart whereas pulses within trains are currently separated by 889 ns. Therefore, continuous sample delivery via fast jets wastes >99% of sample. Here, we introduce a microfluidic device delivering crystal laden droplets segmented with an immiscible oil reducing sample waste and demonstrate droplet injection at the EuXFEL compatible with high pressure liquid delivery of an SFX experiment. While achieving ~60% reduction in sample waste, we determine the structure of the enzyme 3-deoxy-D-manno-octulosonate-8-phosphate synthase from microcrystals delivered in droplets revealing distinct structural features not previously reported.
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