Covalent Immobilization of Peptides on Self-Assembled Monolayer Surfaces Using Soft-Landing of Mass-Selected Ions

2007 ◽  
Vol 129 (28) ◽  
pp. 8682-8683 ◽  
Author(s):  
Peng Wang ◽  
Omar Hadjar ◽  
Julia Laskin

2008 ◽  
Vol 10 (8) ◽  
pp. 1079-1090 ◽  
Author(s):  
Julia Laskin ◽  
Peng Wang ◽  
Omar Hadjar




2008 ◽  
Vol 112 (40) ◽  
pp. 15824-15831 ◽  
Author(s):  
Shuhei Nagaoka ◽  
Kaori Ikemoto ◽  
Takeshi Matsumoto ◽  
Masaaki Mitsui ◽  
Atsushi Nakajima


1998 ◽  
Vol 174 (1-3) ◽  
pp. 193-217 ◽  
Author(s):  
Hai Luo ◽  
Scott A. Miller ◽  
R.Graham Cooks ◽  
Steven J. Pachuta


2006 ◽  
Vol 110 (7) ◽  
pp. 2968-2971 ◽  
Author(s):  
Masaaki Mitsui ◽  
Shuhei Nagaoka ◽  
Takeshi Matsumoto ◽  
Atsushi Nakajima


2016 ◽  
Vol 29 (1) ◽  
pp. 272-279 ◽  
Author(s):  
Reza Karimi Shervedani ◽  
Sonia Bahrani ◽  
Marzieh Samiei Foroushani ◽  
Fariborz Momenbeik


2014 ◽  
Vol 16 (43) ◽  
pp. 23769-23778 ◽  
Author(s):  
Subha Pratihar ◽  
Swapnil C. Kohale ◽  
Dhruv G. Bhakta ◽  
Julia Laskin ◽  
William L. Hase

Combined theoretical/experimental study on the collisions of protonated dialanine with a perfluorinated octanethiolate self-assembled monolayer (F-SAM) surface.



2015 ◽  
Vol 17 (38) ◽  
pp. 24576-24586 ◽  
Author(s):  
S. Pratihar ◽  
N. Kim ◽  
S. C. Kohale ◽  
W. L. Hase

Previous chemical dynamics simulations (Phys. Chem. Chem. Phys., 2014, 16, 23769–23778) were analyzed to delineate mechanistic details of collisional energy transfer and trapping/soft landing for collisions of N-protonated dialanine (ala2-H+) with a C8 perfluorinated self-assembled monolayer.



2009 ◽  
Vol 113 (11) ◽  
pp. 4476-4482 ◽  
Author(s):  
Kaori Ikemoto ◽  
Shuhei Nagaoka ◽  
Takeshi Matsumoto ◽  
Masaaki Mitsui ◽  
Atsushi Nakajima


2011 ◽  
Vol 239-242 ◽  
pp. 1442-1447 ◽  
Author(s):  
Shu Zhen Tan ◽  
Pu Ni Zeng ◽  
Zhong Cao ◽  
Jiao Yun Xia ◽  
Wei Li

A novel technique to covalently immobilize indicator dyes with terminal amino groups for preparing optical sensors is investigated. Au nanoparticles are used as bridges and carriers for anchoring indicator dyes on the surface of a quartz glass slide. 1-Aminopyrene (AP) was employed as an example of indicator dyes and covalently immobilized onto the outmost surface of the glass slide. First, the glass slide was functionalized by (3-mercaptopropyl) trimethoxysilane (MPS) to form a thiol-terminated self-assembled monolayer, where Au nanoparticles were strongly anchored via covalent link. Then, 16-mercaptohexadecanoic acid (MHDA) was self-assembled to bring carboxylic groups onto the surfaces of Au nanoparticles. A further activation by using 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) converted the carboxylic group into succinimide ester. Finally, the active succinimide ester was reacted with 1-aminopyrene (AP). Thus, AP was covalently immobilized to the glass slide and an AP-immobilized sensor was obtained. The resulting sensor was used to determine rutin based on fluorescence quenching. It showed a linear response toward rutin (R) from 5.0 × 10-7 to 6.0 × 10-4 mol L-1 with a detection limit of 2.0× 10-7 mol L-1. This AP-immobilized sensor has very satisfactory reproducibility, reversibility, rapid response and no dye-leaching.



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