000581007 001__ 581007 000581007 005__ 20250715173712.0 000581007 0247_ $$2doi$$a10.3390/cryst13081225 000581007 0247_ $$2datacite_doi$$a10.3204/PUBDB-2023-01521 000581007 0247_ $$2WOS$$aWOS:001055304900001 000581007 0247_ $$2openalex$$aopenalex:W4385708691 000581007 037__ $$aPUBDB-2023-01521 000581007 041__ $$aEnglish 000581007 082__ $$a540 000581007 1001_ $$0P:(DE-H253)PIP1081165$$aGalchenkova, Marina$$b0 000581007 245__ $$aAn Optimized Approach for Serial Crystallography Using Chips 000581007 260__ $$aBasel$$bMDPI$$c2023 000581007 3367_ $$2DRIVER$$aarticle 000581007 3367_ $$2DataCite$$aOutput Types/Journal article 000581007 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1705333764_3778160 000581007 3367_ $$2BibTeX$$aARTICLE 000581007 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000581007 3367_ $$00$$2EndNote$$aJournal Article 000581007 520__ $$aSerial crystallography is a rapidly developing field that makes it possible to determine the structure of biomolecules at room temperature with atomic resolution. Numerous advances in detectors, data analysis pipelines, sample delivery methods, and crystallization protocols expand the scope of structural biology to understand the fundamental processes that take place in living cells. At the same time, all stages of experiments should be maximally optimized to avoid loss of beamtime. Thus, this paper proposes a strategy for optimizing beamtime utilization while using a fixed target sample delivery method such as chips. The strategy consists of two steps: first, a fast raster scan of the chip is performed to determine the positions of the crystals, and then small rotational series are measured at predetermined positions. 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