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. 2022 Oct 1;20:432. doi: 10.1186/s12951-022-01636-x

Fig. 1.

Fig. 1

Screening of phages and identification of positive phage clones. A The titers of the recovered and amplified phages from each round. The blue plaques formed on agar plates containing tetracycline were used to calculated the phages. B Elisa results for 20 phage clones binding to HSC-T6, BRL-3A, NRK-52E, and H9C2 cells. C Following 4 rounds of phage display biopanning, amino acid sequence with highest frequencies was identified by DNA sequencing. The nucleic acid sequences were analyzed by Chromas. DH Comparison of phage cell-binding Elisa results for the affinity of individual phage clones with same sequence (CDGRPDRAC) to HSC-T6, BRL-3A, NRK-52E, and H9C2 cells. IK Molecular structure and mass spectrogram of the HSTP1, rcHSTP1, and TAT. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001