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用于疫苗研发的恶性疟原虫α-螺旋卷曲螺旋结构域中的序列保守性

Sequence conservation in Plasmodium falciparum alpha-helical coiled coil domains proposed for vaccine development.

作者信息

Kulangara Caroline, Kajava Andrey V, Corradin Giampietro, Felger Ingrid

机构信息

Swiss Tropical Institute, Basel, Switzerland.

出版信息

PLoS One. 2009 May 25;4(5):e5419. doi: 10.1371/journal.pone.0005419.

Abstract

BACKGROUND

The availability of the P. falciparum genome has led to novel ways to identify potential vaccine candidates. A new approach for antigen discovery based on the bioinformatic selection of heptad repeat motifs corresponding to alpha-helical coiled coil structures yielded promising results. To elucidate the question about the relationship between the coiled coil motifs and their sequence conservation, we have assessed the extent of polymorphism in putative alpha-helical coiled coil domains in culture strains, in natural populations and in the single nucleotide polymorphism data available at PlasmoDB.

METHODOLOGY/PRINCIPAL FINDINGS: 14 alpha-helical coiled coil domains were selected based on preclinical experimental evaluation. They were tested by PCR amplification and sequencing of different P. falciparum culture strains and field isolates. We found that only 3 out of 14 alpha-helical coiled coils showed point mutations and/or length polymorphisms. Based on promising immunological results 5 of these peptides were selected for further analysis. Direct sequencing of field samples from Papua New Guinea and Tanzania showed that 3 out of these 5 peptides were completely conserved. An in silico analysis of polymorphism was performed for all 166 putative alpha-helical coiled coil domains originally identified in the P. falciparum genome. We found that 82% (137/166) of these peptides were conserved, and for one peptide only the detected SNPs decreased substantially the probability score for alpha-helical coiled coil formation. More SNPs were found in arrays of almost perfect tandem repeats. In summary, the coiled coil structure prediction was rarely modified by SNPs. The analysis revealed a number of peptides with strictly conserved alpha-helical coiled coil motifs.

CONCLUSION/SIGNIFICANCE: We conclude that the selection of alpha-helical coiled coil structural motifs is a valuable approach to identify potential vaccine targets showing a high degree of conservation.

摘要

背景

恶性疟原虫基因组的可得性带来了鉴定潜在疫苗候选物的新方法。一种基于对与α-螺旋卷曲螺旋结构相对应的七肽重复基序进行生物信息学选择的抗原发现新方法产生了有前景的结果。为了阐明卷曲螺旋基序与其序列保守性之间关系的问题,我们评估了培养菌株、自然种群以及疟原虫数据库(PlasmoDB)中可用的单核苷酸多态性数据中假定的α-螺旋卷曲螺旋结构域的多态性程度。

方法/主要发现:基于临床前实验评估选择了14个α-螺旋卷曲螺旋结构域。通过对不同的恶性疟原虫培养菌株和野外分离株进行PCR扩增和测序对它们进行检测。我们发现14个α-螺旋卷曲螺旋中只有3个显示出点突变和/或长度多态性。基于有前景的免疫学结果,选择了其中5个肽进行进一步分析。对来自巴布亚新几内亚和坦桑尼亚的野外样本进行直接测序表明,这5个肽中有3个是完全保守的。对最初在恶性疟原虫基因组中鉴定出的所有166个假定的α-螺旋卷曲螺旋结构域进行了多态性的计算机分析。我们发现这些肽中有82%(137/166)是保守的,并且对于一个肽,仅检测到的单核苷酸多态性就大大降低了α-螺旋卷曲螺旋形成的概率得分。在几乎完美的串联重复序列阵列中发现了更多的单核苷酸多态性。总之,卷曲螺旋结构预测很少因单核苷酸多态性而改变。分析揭示了许多具有严格保守的α-螺旋卷曲螺旋基序的肽。

结论/意义:我们得出结论,选择α-螺旋卷曲螺旋结构基序是鉴定显示高度保守性的潜在疫苗靶点的一种有价值的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d392/2683929/5a6b7bbf720e/pone.0005419.g001.jpg

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