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. 2022 Oct 6;13:5879. doi: 10.1038/s41467-022-33662-6

Fig. 7. HIV-1 infectivity assays probing a role of Pro residues in the context of CPSF6(LCR-FG-LCR).

Fig. 7

a Schematic of WT and mutant CPSF61-358 constructs. Amino acid sequences of the CPSF6(LCR-FG-LCR) segment targeted by mutagenesis are shown. CPSF6358/WT: native Pro residues are in bold and underlined. The FG containing peptide is highlighted in green. CPSF6358(ΔFG): FG residues were deleted. CPSF6358/mP-FGp: Pro residues in the FG-containing peptide were substituted with Gly or Ser. CPSF6358/mP-LCR: Pro residues in the LCR segments were substituted with non-charged residues. CPSF6358/mP-ED: Pro residues in the LCR segments were substituted with charged residues Glu or Asp. CPSF6358/NE: the LCR segments of CPSF6358 were replaced with non-LCR counterparts from NEURM97-179. CPSF6358/FU: the LCR segments of CPSF6358 were replaced with alternative LCR from FUS35-117. CPSF6358(ΔFG)/FU: FG residues were deleted from CPSF6358/FU. b Relative infectivity of VSV-G pseudotyped HIV-1 in the Hela cells stably overexpressing proteins shown in a. Infectivity was normalized to CPSF6358(ΔFG). The averaged data (+/− SD) from three independent experiments are shown. Source data are provided as a Source Data file.