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Data · dataset · 2026

<p>Grass carp NHRE3 interacts with ISG15.</p>

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<p>(A) Non-specific proteins identified via immunoprecipitation–mass spectrometry (IP–MS) in the control group (NHRE3 overexpression without viral challenge).

Description

(B) Candidate interacting proteins identified via IP–MS in the experimental group (NHRE3 overexpression with viral challenge). (C) Venn diagram of proteins identified with IP–MS in the control and experimental groups.

After excluding 23 non-specific proteins found in the control group, six candidate interacting proteins were identified in the experimental group. (D) Annotation information for the six candidate interacting proteins. (E) Co-immunoprecipitation (Co-IP) was performed 24 h after co-transfection of pcDNA-NHRE3-HA and pCMV-ISG15-MYC in 293T cells.

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A distinct band was observed in the IP fraction corresponding to the interaction between NHRE3 and ISG15. (F) Colocalization analysis was performed 24 h after co-transfection of pGFP-NHRE3 and pmCherry-ISG15 in CIK cells. Confocal microscopy revealed cytoplasmic colocalization, which was confirmed by analysis using the ImageJ Colocalization Finder plugin, yielding a Pearson correlation coefficient of 0.57.

(G) Domain structure of NHRE3 and construction of truncation mutants. (H) Co-IP was performed 24 h after co-transfection of NHRE3_N and NHRE3_C truncation mutants with pCMV-ISG15-MYC in 293T cells. A distinct band was observed in the IP fraction corresponding to the interaction between the NHRE3_C mutant and ISG15.

All experiments were repeated for at least three times with similar results.</p>

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Inferred from text
Mass spectrometry 75% · Microscopy 75%
Provenance · 1 source records, 19 field assertions
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