کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5741047 1616985 2017 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Full length articleTranscript and protein expression analysis of proteases in the blood stages of Plasmodium falciparum
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی انگل شناسی
پیش نمایش صفحه اول مقاله
Full length articleTranscript and protein expression analysis of proteases in the blood stages of Plasmodium falciparum
چکیده انگلیسی


- Plasmodium falciparum database mining identifies about 148 putative proteases.
- Transcript expression profiling of selected proteases shows stage-specific expression of proteases.
- Protein expression analysis of selected proteases confirms their stage-specific expression.
- P. falciparum proteases represent ideal targets for stage-specific or multi-stage drugs.

Proteases are crucial enzymes with varying roles in living organisms. In the malaria parasite Plasmodium falciparum, the role of proteases has been deciphered mainly in the asexual blood stages and shown to represent promising drug targets. However, little is known about their functions in the sexual blood stages, which are important for transmission of the disease from the human to the mosquito vector. Determination of their stage-specific expression during the malaria life-cycle is crucial for the effective design of multi-stage anti-malaria drugs aimed at eradicating the disease. In this study, we screened the P. falciparum genome database for putative proteases and determined the transcript and protein expression profiles of selected proteases in the plasmodial blood stages using semi-quantitative RT-PCR and indirect immunofluorescence assay. Database mining identified a total of 148 putative proteases, out of which 18 were demonstrated to be expressed in the blood stages on the transcript level; for 12 of these proteins synthesis was confirmed. While three of these proteases exhibit gametocyte-specific expression, two are restricted to the asexual blood stages and seven are found in both stages, making them interesting multi-stage drug targets.

111

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Parasitology - Volume 180, September 2017, Pages 33-44
نویسندگان
, , , , ,