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We compare serial femtosecond crystallography data from hemoglobin crystals using 3 and 10\u2005fs pulses at comparable peak intensities (\u223c3 \u00d7 10\n                    <jats:sup>17<\/jats:sup>\n                    \u2005W\u2005cm\n                    <jats:sup>\u22122<\/jats:sup>\n                    ) and fixed photon energy (7.15\u2005keV). Structural refinement produced very similar models and resolution-dependent data-quality indicators remained comparable. Both datasets also retained sufficient anomalous signal for phasing. These observations support the conclusion that high-resolution scattering was preserved under both pulse durations. Hybrid collisional\u2013radiative and molecular-dynamics simulations show that under typical experimental conditions, atomic form-factor changes are negligible (&lt;1%) and atomic displacements fall below the resolution limit imposed by the X-ray photon energy and the geometry of the detector. The combined experimental and theoretical results indicate that 10\u2005fs pulses are adequate to obtain damage-free protein structures using femtosecond crystallography under the intensity conditions explored.\n                  <\/jats:p>","DOI":"10.1107\/s2059798326008569","type":"journal-article","created":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T10:00:22Z","timestamp":1789034422000},"page":"1169-1180","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":0,"title":["Radiation damage in serial femtosecond crystallography studied in hemoglobin"],"prefix":"10.1107","volume":"82","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0978-5695","authenticated-orcid":true,"given":"Marina","family":"Galchenkova","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01js2sh04","id-type":"ROR","asserted-by":"publisher"}],"department":["Center for Free-Electron Laser Science 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