Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain
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Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain
Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain
解放军医学杂志(英文版)1993年第3期 页码:246-253
Affiliations:
1. Institute of Medical Biotechnology and Molecular Genetics Second Military Medical University
2. ,200433
Author bio:
Funds:
This study was supported by UNDP/WORLD BANK/WHO Special Programme for Research and Training in Tropical Diseases(TDR),ID No.910265
DOI:
中图分类号:
纸质出版:1993
Accepted:
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Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain[J]. 解放军医学杂志(英文版), 1993,(3):246-253.
[1]杨树桐,潘卫庆,邓海琳,陆德如.Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain[J].Journal of Medical Colleges of PLA,1993(03):246-253.
Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain[J]. 解放军医学杂志(英文版), 1993,(3):246-253.DOI:
[1]杨树桐,潘卫庆,邓海琳,陆德如.Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain[J].Journal of Medical Colleges of PLA,1993(03):246-253.DOI:
Subcloning,sequencing and expressing of conserved blocks of P190 gene of Plasmodium falciparum FCC1/HN strain
摘要
Abstract
<正> 190-kilodalton glycoprotein (P190) of Plasmodium falciparum
precursor of themajor surface protein of merozoites
is considered a promising candidate for blood stage malarialvaccine.Six primers were designed according to the sequence of MAD20 strain
with a GCclamp and BamH Ⅰ site at the 5’-end of each one
and a GC clamp and Xba Ⅰ site at the 3’-endof each one.The primers were synthesized by phosphoramidite approach (User’s Manual ofABI Company) and purified using HPLC.Three fragments in the second
third and fourth con-served regions of P190 gene of Plasrnodium falciparum FCC1/HN strain isolated from theblood of patients in Hainan Province of China were amplified by the polymerase chain reaction(PCR).The amplified fragments were suhcloned into pUC18 vectors and sequenced using thedideoxy chain termination method.All three regions of P190 gene of FCC1/HN strain also werehighly conservative as compared with P190 gene of MAD20 (Papua New Guinea isolate)
K1(Thailand isolate)
Wellcome (West Africa isolate) and CAMP (Malaysia) strains ofPlasmodium falciparum.The C at position 81 in the second conserved block of P190 gene ofFCC1/HN isolate was substituted by T
which did not change the amino acid determined by thecodon corresponding to the substitution.The genes sequenced were cloned into rpGEX-2T
aglutathione S-transferase gene fusion system for expression.
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