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From
Identification of Novel Multi Epitopes Vaccine against the Capsid Protein (
ORF2
) of Hepatitis E Virus
Mashair A. A. Nouri, Yassir A. Almofti, Khoubieb Ali Abd-elrahman, Elsideeq E. M. Eltilib
American Journal of Infectious Diseases and Microbiology
.
2019
, 7(1), 26-42 doi:10.12691/ajidm-7-1-5
Figure
1.
Evolutionary divergence analysis of capsid protein of the HEV. The retrieved strains showed divergence in their common ancestors
Full size figure and legend
Figure
2.
Multiple sequence alignment (MSA) of the retrieved strains using Bioedit software and ClustalW. Dots indicated the conservancy and letters in cubes showed the alteration in amino acid
Full size figure and legend
Figure
3.
Prediction of B-cell epitopes using (a) Bepipred linear epitope, threshold value 0.353 (b) Emini surface accessibility, threshold value 1.000 and (c) Kolaskar & Tongaonkar antigenicity methods, threshold value 1.031. Yellow areas above the threshold (red line) are suggested to be a part of B cell epitope, while green areas are not
Full size figure and legend
Figure
4.
Position of proposed conserved B cell epitopes in structural level of the capsid protein. Five epitopes were illustrated in this figure to interact with B cell. These epitopes showed conservancy, high score in surface accessibility and antigenicity using IEDB software. The ball like structures represent the predicted epitopes. The position of these epitopes was according to their position in the capsid protein
Full size figure and legend
Figure
5.
T cell proposed epitopes that interact with MHC-I alleles. These epitopes are
367
GIALTLFNL
375
,
379
LLGGLPTEL
387
,
394
QLFYSRPVV
402
and
389
SSAGGQLFY
397
. The first three epitopes
were found interacting with both MHC-1 and MHC-II alleles. The latter interacted only with MHC-I alleles and it was shown in figure (6). The ball like structures represent the predicted epitopes. The positions of these proposed epitopes was according to their position in the capsid protein of HEV
Full size figure and legend
Figure
6.
T cell proposed epitopes that interact with MHC-II alleles. These epitopes were
205
YAISISFWP
213
,
299
LLDFALELE
307
,
341
LTTTAATRF
349
,
368
IALTLFNLA
376
,
367
GIALTLFNL
375
,
379
LLGGLPTEL
387
and
394
QLFYSRPVV
402
. The last three epitopes were shown in Figure 5.
The epitope
389
SSAGGQLFY
397
also interacted with MHC-1 alleles. The ball like structures represent the predicted epitopes. The positions of these proposed epitopes was according to their position in the capsid protein of HEV
Full size figure and legend