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Paper-scoped peptide mentionSequence not reported or unresolved

MPI-C

PMC10043419::PEP000002

Source publication

Bioengineered bacterial outer membrane vesicles encapsulated Polybia–mastoparan I fusion peptide as a promising nanoplatform for bladder cancer immune-modulatory chemotherapy

Frontiers in Immunology · 2023

Sequence status
not reported or unresolved
Standardization
Sequence unresolved
Source location
unknown
Activity records
7

Sequence evidence

Reported molecular identity

The publication reports a peptide label or compound identity, but no sequence could be safely standardized from the available text, table, figure, or structure context.

Fusion protein with MPI at the C terminal (MPI-C). The gene encoding eGFP was amplified ... and inserted into pET43.1a ... Subsequently, the synthesized DNA sequence of MPI including a terminator TAA ... was attached behind eGFP gene.

Experimental observations

Records linked to this mention

AnticancerCytotoxicPositive observation
Record detail

Both of them had a pronounced reduction of their viabilities when treated with bioengineered OMVs ... while OMV^MPI-C had the lowest half-maximal inhibitory concentration (IC50) (Figures 2B, C).

Measure
other
Value
lowest IC50
Target
MB49
Assay
Not reported by source
Source publication
AnticancerCytotoxicPositive observation
Record detail

Both of them had a pronounced reduction of their viabilities when treated with bioengineered OMVs ... while OMV^MPI-C had the lowest half-maximal inhibitory concentration (IC50) (Figures 2B, C).

Measure
other
Value
lowest IC50
Target
UMUC3
Assay
Not reported by source
Source publication
AnticancerCytotoxicPositive observation
Record detail

The results presented in Figure 2F manifested the percentage of apoptotic MB49 cells increased to 44.3% in OMV^MPI-C group, much higher than the 8.43% in PBS group and 11.0% in OMV^WT group.

Measure
percent_inhibition
Value
44.3%
Target
MB49
Assay
Not reported by source
Source publication
AnticancerCytotoxicNegative / threshold
Record detail

However, a non-carcinomatous cell named bEnd.3 ... exhibited no viability suppression when being treated with different OMVs at the concentration of <100 μg/ml (Figure S5), indicating the specific destruction ability of MPI fusion peptides in bioengineered OMVs to tumor cells.

Mention PMC10043419::PEP000002PMC10043419supplement
Measure
cell_viability
Value
no viability suppression at <100 μg/ml
Target
bEnd.3
Assay
Not reported by source
Source publication
AnticancerCytotoxicPositive observation
Record detail

Tumor growth curves shown in Figure 3C depicted different therapy efficacies of OMVs ... OMV^MPI-SP and OMV^MPI-C treatments resulted in better therapeutic outcomes with statistical significance when compared with the PBS group.

Measure
survival_rate
Value
tumor growth restricted
Target
Mus musculus
Assay
Not reported by source
Source publication
ToxicityHemolyticNegative / threshold
Record detail

After incubation ... the calculated hemolysis ratio of OMV groups was lower than 5% (Figures 5A, B), indicating the negligible hemolysis caused by bioengineered OMVs in vitro.

Measure
hemolysis
Value
<5%
Target
Mus musculus
Assay
Not reported by source
Source publication

Local peptide labels such as P1, PEP1, or peptide 1 are grouped only within this paper and are not assumed to represent the same molecule across publications.