Site‐Specific DNA‐Programmed Growth of Fluorescent and Functional Silver Nanoclusters

2011 ◽  
Vol 17 (13) ◽  
pp. 3774-3780 ◽  
Author(s):  
Zhenzhen Huang ◽  
Fang Pu ◽  
Dan Hu ◽  
Chunyan Wang ◽  
Jinsong Ren ◽  
...  
2011 ◽  
Vol 123 (18) ◽  
pp. 4262-4265 ◽  
Author(s):  
Suchetan Pal ◽  
Reji Varghese ◽  
Zhengtao Deng ◽  
Zhao Zhao ◽  
Ashok Kumar ◽  
...  

2012 ◽  
Vol 724 ◽  
pp. 86-91 ◽  
Author(s):  
Qinghua Cui ◽  
Kun Ma ◽  
Yong Shao ◽  
Shujuan Xu ◽  
Fei Wu ◽  
...  

2012 ◽  
Vol 40 (16) ◽  
pp. e122-e122 ◽  
Author(s):  
Lingyan Feng ◽  
Zhenzhen Huang ◽  
Jinsong Ren ◽  
Xiaogang Qu

2011 ◽  
Vol 50 (18) ◽  
pp. 4176-4179 ◽  
Author(s):  
Suchetan Pal ◽  
Reji Varghese ◽  
Zhengtao Deng ◽  
Zhao Zhao ◽  
Ashok Kumar ◽  
...  

2018 ◽  
Vol 140 (3) ◽  
pp. 1069-1076 ◽  
Author(s):  
Zhao-Yang Wang ◽  
Meng-Qi Wang ◽  
Yan-Ling Li ◽  
Peng Luo ◽  
Tong-Tong Jia ◽  
...  

Author(s):  
Richard D. Powell ◽  
James F. Hainfeld ◽  
Carol M. R. Halsey ◽  
David L. Spector ◽  
Shelley Kaurin ◽  
...  

Two new types of covalently linked, site-specific immunoprobes have been prepared using metal cluster labels, and used to stain components of cells. Combined fluorescein and 1.4 nm “Nanogold” labels were prepared by using the fluorescein-conjugated tris (aryl) phosphine ligand and the amino-substituted ligand in the synthesis of the Nanogold cluster. This cluster label was activated by reaction with a 60-fold excess of (sulfo-Succinimidyl-4-N-maleiniido-cyclohexane-l-carboxylate (sulfo-SMCC) at pH 7.5, separated from excess cross-linking reagent by gel filtration, and mixed in ten-fold excess with Goat Fab’ fragments against mouse IgG (obtained by reduction of F(ab’)2 fragments with 50 mM mercaptoethylamine hydrochloride). Labeled Fab’ fragments were isolated by gel filtration HPLC (Superose-12, Pharmacia). A combined Nanogold and Texas Red label was also prepared, using a Nanogold cluster derivatized with both and its protected analog: the cluster was reacted with an eight-fold excess of Texas Red sulfonyl chloride at pH 9.0, separated from excess Texas Red by gel filtration, then deprotected with HC1 in methanol to yield the amino-substituted label.


2020 ◽  
Vol 64 (1) ◽  
pp. 135-153 ◽  
Author(s):  
Lauren Elizabeth Smith ◽  
Adelina Rogowska-Wrzesinska

Abstract Post-translational modifications (PTMs) are integral to the regulation of protein function, characterising their role in this process is vital to understanding how cells work in both healthy and diseased states. Mass spectrometry (MS) facilitates the mass determination and sequencing of peptides, and thereby also the detection of site-specific PTMs. However, numerous challenges in this field continue to persist. The diverse chemical properties, low abundance, labile nature and instability of many PTMs, in combination with the more practical issues of compatibility with MS and bioinformatics challenges, contribute to the arduous nature of their analysis. In this review, we present an overview of the established MS-based approaches for analysing PTMs and the common complications associated with their investigation, including examples of specific challenges focusing on phosphorylation, lysine acetylation and redox modifications.


1987 ◽  
Vol 48 (C9) ◽  
pp. C9-741-C9-744 ◽  
Author(s):  
W. HABENICHT ◽  
L. A. CHEWTER ◽  
M. SANDER ◽  
K. MÜLLER-DETHLEFS ◽  
E. W. SCHLAG

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