Rapid Identification of Fluorochrome Modification Sites in Proteins by LC ESI-Q-TOF Mass Spectrometry-Reference-Cited by-同舟云学术

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Rapid Identification of Fluorochrome Modification Sites in Proteins by LC ESI-Q-TOF Mass Spectrometry

Published:2011-06-07 Issue:7 Volume:22 Page:1330-1336
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Manikwar Prakash¹,Zimmerman Tahl²,Blanco Francisco J.²³,Williams Todd D.⁴,Siahaan Teruna J.¹

Affiliation:

1. Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, Kansas 66047, United States

2. Unidad de Biología Estructural, CIC bioGUNE, 48160 Derio, Bizkaia, Spain

3. IKERBASQUE, Basque Foundation for Science, 48011 Bilbao, Spain

4. Mass Spectrometry Laboratory, University of Kansas, Lawrence, Kansas 66045, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/bc100560c

Reference29 articles.

1. [9] Quantitative fluorometric assay for detection and characterization of Fc receptors

2. Reaction of Fluorescein Isothiocyanate with Thiol and Amino Groups of Sarcoplasmic ATPase

3. Crystal structure of the I-domain from the CD11a/CD18 (LFA-1, alpha L beta 2) integrin.

4. Structures of the αL I Domain and Its Complex with ICAM-1 Reveal a Shape-Shifting Pathway for Integrin Regulation

5. The I Domain of Integrin LFA-1 Interacts with ICAM-1 Domain 1 at Residue Glu-34 but Not Gln-73

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