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Furthermore, such heterotypic interactions do not necessitate classical -sheet-rich amyloid fibril formation, but rather favor amorphous, lipidrich, and membranedense inclusions

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We also examined the role of glycosylation by introducing asparagine-to-alanine substitutions at six different potential N -glycosylation sites in surface-targeted LacAnc100, none of which appeared to notably reduce its activity (Supplementary Fig

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