کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
877694 911041 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Nanoprobing of α-synuclein misfolding and aggregation with atomic force microscopy
موضوعات مرتبط
مهندسی و علوم پایه سایر رشته های مهندسی مهندسی پزشکی
پیش نمایش صفحه اول مقاله
Nanoprobing of α-synuclein misfolding and aggregation with atomic force microscopy
چکیده انگلیسی

Atomic force microscopy (AFM) force spectroscopy is a technique with broad nanomedical applications, widely used for the characterization of molecular interactions on the nanoscale. Here we test this technique to evaluate compounds for influencing the protein aggregation process. The results demonstrate that Zn2+ or Al3+ cations bring about a dramatic increase of α-synuclein interactions in unfavorable conditions for α-synuclein misfolding (neutral pH). We did not observe the effect of dopamine at favorable conditions for α-synuclein misfolding (acidic pH). We also found that electrostatic interactions do not play a significant role at acidic pH. These findings are generally in line with previous studies by various techniques. The high sensitivity of AFM force spectroscopy as well as its ability to test compounds for the same experimental system makes AFM an efficient nanotool for rapid analysis of compounds inhibiting early protein aggregation studies and quantitative selection of potential therapeutics for neurodegenerative diseases.From the Clinical EditorAtomic force microscopy is used to interrogate the influence of cations and α-synuclein on the protein aggregation process. The report illustrates an application of AFM to unravel the potential of novel therapeutics on early protein aggregation intrinsic in neurodegenerative diseases.

Graphical AbstractAFM force spectroscopy is a technique with broad nanomedical applications, widely used for the characterization of molecular interactions at nanoscale level. Here we test this technique to evaluate compounds for influencing the protein aggregation process. The results demonstrate that Zn2+ or Al3+ cations lead to a dramatic increase of α-synuclein interactions in unfavorable conditions for α-synuclein misfolding (neutral pH). We did not observe the effect of dopamine at favorable condition for α-synuclein misfolding (acidit pH). We also found that electrostatic interactions do not play a significant role at acidic pH. These findings are generally in line with previous studies by various techniques. The high sensitivity of AFM force spectroscopy as well as its ability to test compounds for the same experimental system makes AFM an efficient nanotool for rapid analysis of compounds inhibiting early protein aggregation studies and uantitative selection of potential therapeutics for neurodegenerative diseases.Figure optionsDownload high-quality image (63 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Nanomedicine: Nanotechnology, Biology and Medicine - Volume 7, Issue 2, April 2011, Pages 146–152
نویسندگان
, , ,