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It is demonstrated that TEMI overcomes the long-standing spatial limitations of MSI without requiring hardware modifications, ensuring compatibility with existing MSI instruments and promoting broad accessibility and adoption within the research community.
These findings reveal that the RSV F antigen recognizes both the wild-type and AAS-mutated bispecific antibodies in a conformation-dependent manner, with binding preferentially observed for larger conformations.
This work provides a foundational framework for optimizing spectral library selection in neuropeptidomics and underscores the importance of model-specific biases when analyzing structurally diverse endogenous peptides.
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