Label-free molecular binding assays using holographic video microscopy

Author(s):  
Fook Chiong Cheong ◽  
David G. Grier
Lab on a Chip ◽  
2005 ◽  
Vol 5 (9) ◽  
pp. 959 ◽  
Author(s):  
Po Ki Yuen ◽  
Norman H. Fontaine ◽  
Mark A. Quesada ◽  
Prantik Mazumder ◽  
Richard Bergman ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Stefan D. Krämer ◽  
Johannes Wöhrle ◽  
Philipp A. Meyer ◽  
Gerald A. Urban ◽  
Günter Roth

Abstract Analogous to a photocopier, we developed a DNA microarray copy technique and were able to copy patterned original DNA microarrays. With this process the appearance of the copied DNA microarray can also be altered compared to the original by producing copies of different resolutions. As a homage to the very first photocopy made by Chester Charlson and Otto Kornei, we performed a lookalike DNA microarray copy exactly 80 years later. Those copies were also used for label-free real-time kinetic binding assays of apo-dCas9 to double stranded DNA and of thrombin to single stranded DNA. Since each DNA microarray copy was made with only 5 µl of spPCR mix, the whole process is cost-efficient. Hence, our DNA microarray copier has a great potential for becoming a standard lab tool.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Yvonne Zagzag ◽  
M. Francesca Soddu ◽  
Andrew D. Hollingsworth ◽  
David G. Grier

2014 ◽  
Vol 5 (11) ◽  
pp. 4375-4381 ◽  
Author(s):  
Yan Guan ◽  
Xiaonan Shan ◽  
Shaopeng Wang ◽  
Peiming Zhang ◽  
Nongjian Tao

We report a charge sensitive optical detection technique for the label-free study of molecular interactions.


2014 ◽  
Vol 19 (03) ◽  
pp. 1 ◽  
Author(s):  
Srikanth V. Kesavan ◽  
Fabrice P. Navarro Y Garcia ◽  
Mathilde Menneteau ◽  
Frédérique Mittler ◽  
Brigitte David-Watine ◽  
...  

1998 ◽  
Vol 3 (3) ◽  
pp. 231-236 ◽  
Author(s):  
Evelyn Good ◽  
Scott Perschke ◽  
Rani Lopez ◽  
Sonia Chang ◽  
April Kinsler ◽  
...  

Cell lines provide a readily available source of target material for functional and molecular binding screens in drug discovery. The Cell PROFILE® program at NovaScreen® represents an effort to identify receptors and enzymes expressed in established cell lines that are relevant to important drug screening endeavors. In this report, we present data on a selected number of receptors and enzymes for four cell lines studied in this survey. The objective of this survey was not to compare one cell line with another, but to illustrate the diversity of pharmacologic targets and the untapped potential of databases for readily obtainable cell lines. The following cell lines, which are all derived from human tumors, were included in this study (with some relevant pharmacologic/pathologic targets): HT-29, derived from an adenocarcinoma of the colon (colorectal cancer); SK-N-MC, derived from a neuroepithelioma (NPY receptors, apoptosis, HIV type I infection); H-4, derived from a neuroglioma (Alzheimer's disease); and LNCaP, derived from a prostate carcinoma (androgen receptor, prostate cancer). Specific to this survey were receptor-binding assays for androgens, corticotropin-releasing factor, endothelin, GABA, NMDA, somatostatin, and alpha and beta adrenergic ligands, as well as binding sites for ion channels. A comparison of specific binding of these various sites between target tissues routinely used in our assays and established cell lines reveals a diversity of receptors heretofore not reported for the latter and represents a potential database for screening and pharmacologic research.


2009 ◽  
Vol 23 (S1) ◽  
Author(s):  
Matthew Wayne Olson ◽  
Jukka Kervinen ◽  
Carsten Schubert ◽  
Jennifer Kirkpatrick ◽  
James Kranz ◽  
...  

2009 ◽  
Vol 17 (15) ◽  
pp. 13071 ◽  
Author(s):  
Fook Chiong Cheong ◽  
Bo Sun Rémi Dreyfus ◽  
Jesse Amato-Grill ◽  
Ke Xiao ◽  
Lisa Dixon ◽  
...  

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