Mutational Analysis of Ocriplasmin to Reduce Proteolytic and Autolytic Activity in Pichia pastoris
Mutational Analysis of Ocriplasmin to Reduce Proteolytic and Autolytic Activity in Pichia pastoris
نویسندگان: رقیه باغبان , صفر فرج نیا , نصرت اله ضرغامی , اعظم صفری
کلمات کلیدی: Ocriplasmin, Pichia pastoris, Site-directed mutagenesis, Proteolytic activity, Autolytic activity
نشریه: 4652 , 25 , 22 , 2020
| نویسنده ثبت کننده مقاله |
صفر فرج نیا |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات بیوتکنولوژی(زیست فناوری) |
| کد مقاله |
74693 |
| عنوان فارسی مقاله |
Mutational Analysis of Ocriplasmin to Reduce Proteolytic and Autolytic Activity in Pichia pastoris |
| عنوان لاتین مقاله |
Mutational Analysis of Ocriplasmin to Reduce Proteolytic and Autolytic Activity in Pichia pastoris |
| ناشر |
7 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
بلی |
| عنوان نشریه (خارج از لیست فوق) |
|
| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| Background: Ocriplasmin (Jetrea) is using for the treatment of symptomatic vitreomacular adhesion. This enzyme
undergoes rapid inactivation and limited activity duration as a result of its autolytic nature after injection within the
eye. Moreover, the proteolytic activity can cause photoreceptor damage, which may result in visual impairment in
more serious cases.
Results: The present research aimed to reduce the disadvantages of ocriplasmin using site-directed mutagenesis.
To reduce the autolytic activity of ocriplasmin in the first variant, lysine 156 changed to glutamic acid and, in the
second variant for the proteolytic activity reduction, alanine 59 mutated to threonine. The third variant contained
both mutations. Expression of wild type and three mutant variants of ocriplasmin constructs were done in the
Pichia pastoris expression system. The mutant variants were analyzed in silico and in vitro and compared to the wild
type. The kinetic parameters of ocriplasmin variants showed both variants with K156E substitution were more
resistant to autolytic degradation than wild-type. These variants also exhibited reduced Kcat and Vmax values. An
increase in their Km values, leading to a decreased catalytic efficiency (the Kcat/Km ratio) of autolytic and mixed
variants. Moreover, in the variant with A59T mutation, Kcat and Vmax values have reduced compared to wild type.
The mix variants showed the most increase in Km value (almost 2-fold) as well as reduced enzymatic affinity to the
substrate. Thus, the results indicated that combined mutations at the ocriplasmin sequence were more effective
compared with single mutations.
Conclusions: The results indicated such variants represent valuable tools for the investigation of therapeutic
strategies aiming at the non-surgical resolution of vitreomacular adhesion. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Baghban2020_Article_MutationalAnalysisOfOcriplasmi.pdf | 1399/10/06 | 2274001 | دانلود |