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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Dual “Click-On” phage display for nanoscaffolds with discretely tunable lateral display density</dc:title><dc:creator>Gnidovec,	Klemen	(Avtor)
	</dc:creator><dc:creator>Ulčakar,	Liza	(Avtor)
	</dc:creator><dc:creator>Bozovičar,	Krištof	(Avtor)
	</dc:creator><dc:creator>Romih,	Rok	(Avtor)
	</dc:creator><dc:creator>Ljubetič,	Ajasja	(Avtor)
	</dc:creator><dc:creator>Bratkovič,	Tomaž	(Avtor)
	</dc:creator><dc:subject>filamentous phage</dc:subject><dc:subject>nanoscaffold</dc:subject><dc:subject>dual display</dc:subject><dc:subject>signal sequence</dc:subject><dc:subject>split protein</dc:subject><dc:subject>SpyTag/SpyCatcher</dc:subject><dc:subject>SnoopTag/SnoopCatcher</dc:subject><dc:description>Filamentous bacteriophages are monodisperse, high-aspect-ratio protein nanofibers that provide a scalable and genetically addressable platform for biohybrid nanomaterials. However, direct fusion of heterologous proteins to capsid proteins often disrupts assembly and limits high-density functionalization to short peptides. Here, we report a dual-display “type 388” phage vector enabling orthogonal and adjustable surface functionalization. SnoopTag was fused to the minor coat protein p3 for low-valency tip display, while SpyTag variants were displayed on the major coat protein p8 for sidewall presentation. Using fluorescent and immunochemical methods, and high-resolution microscopy techniques, we show that the lateral display density on p8 can be discretely adjusted by selecting distinct signal sequence-SpyTag combinations that modulate the efficiency of bacterial inner membrane integration and capsid incorporation. Replacement of the native p8 signal sequence with a signal recognition particle-compatible counterpart enhances functional display, enabling adjustable multivalent patterning. Orthogonal Tag/Catcher pairs and post-assembly cargo conjugation together establish a plug-and-play, anisotropic nanoscaffold for precision biofunctionalization. As a proof of concept, the phage nanotemplate was functionalized with targeting and reporter modules to generate an antibody-mimetic probe for analyte detection.</dc:description><dc:date>2026</dc:date><dc:date>2026-11-10 07:32:47</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>190990</dc:identifier><dc:identifier>UDK: 66.017-022.513.2:620.3</dc:identifier><dc:identifier>ISSN pri članku: 2574-0970</dc:identifier><dc:identifier>DOI: 10.1021/acsanm.6c02379</dc:identifier><dc:identifier>COBISS_ID: 304353539</dc:identifier><dc:language>sl</dc:language></metadata>
