Protein engineering: Regulatory perspectives of stearoyl CoA desaturase

被引:24
|
作者
Kamal, Shagufta [1 ]
Saleem, Ayesha [1 ]
Rehman, Saima [2 ]
Bibi, Ismat [3 ]
Iqbal, Hafiz M. N. [4 ]
机构
[1] Govt Coll Univ, Dept Biochem, Faisalabad 38000, Pakistan
[2] Govt Coll Univ, Dept Chem, Faisalabad 38000, Pakistan
[3] Islamia Univ, Dept Chem, Bahawalpur 63100, Pakistan
[4] Tecnol Monterrey, Sch Sci & Engn, Campus Monterrey,Ave Eugenio Garza Sada 2501, Monterrey 64849, NL, Mexico
关键词
Protein engineering; Stearoyl CoA desaturase; Isoforms; Desaturase index; Regulation; Metabolic disorders; FATTY-ACID-COMPOSITION; GREEN TEA; INSULIN-RESISTANCE; GENE-EXPRESSION; TRANSCRIPTION FACTOR; METABOLIC SYNDROME; HEPATIC STEATOSIS; ADIPOSE-TISSUE; RISK-FACTORS; CHIA SEED;
D O I
10.1016/j.ijbiomac.2018.03.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stearoyl Co A desaturase (SCD) is a rate-limiting lipogenic enzyme that plays an integral role in catalyzing the synthesis of monounsaturated fatty acids, chiefly oleate and palmitoleate. Both contribute a major part of the biological membrane. Numerous SCD isoforms exist in mouse and humans, i.e., SCD-1 to SCD-4 and SCD-1 and SCD-5, respectively. From the biological viewpoint, hyperexpression of SCD1 cause many metabolic disorders including obesity, insulin resistance, hypertension, and hypertriglyceridemia, etc. Herein, an effort has been made to highlight the value of protein engineering in controlling the SCD-1 expression with the involvement of different inhibitors as therapeutic agents. The first part of the review describes Stearoyl CoA desaturase index and different SCD isoforms. Various regulatory aspects of SCD are reviewed in four subsections, i.e., (1) hormonal regulation, (2) regulation by dietary carbohydrates, (3) regulation by green tea, and (4) regulation via polyunsaturated fatty acids (PUFAs). Moreover, the regulation of Stearoyl CoA desaturase expression in the metabolism of fats and carbohydrates is discussed. The third part mainly focuses on natural and synthetic inhibitors. Towards the end, information is also given on potential future considerations of SCD-1 inhibitors as metabolic syndrome therapeutics, yet additional work is required. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:692 / 699
页数:8
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