Affinity Chromatographic Method for Determining Drug–Protein Interaction with Enhanced Speed Than Typical Frontal Analysis-Reference-Cited by-同舟云学术

Affinity Chromatographic Method for Determining Drug–Protein Interaction with Enhanced Speed Than Typical Frontal Analysis

Published:2023-07-16 Issue:29 Volume:39 Page:10259-10269
ISSN:0743-7463
Container-title:Langmuir
language:en
Short-container-title:Langmuir

Author:

Ou Yuanyuan¹,Qiao Sai¹,Li Ting¹,Zheng Xinxin¹,Zhao Xue¹,Qu Lejing¹,Zhao Xinfeng¹^ORCID,Zhang Yajun¹^ORCID

Affiliation:

1. Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, College of Life Sciences, Northwest University, Xi’an 710069, China

Funder

Shaanxi Administration of Traditional Chinese Medicine

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Electrochemistry,Spectroscopy,Surfaces and Interfaces,Condensed Matter Physics,General Materials Science

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.langmuir.3c01340

Reference46 articles.

1. Precise assembly of inside-out cell membrane camouflaged nanoparticles via bioorthogonal reactions for improving drug leads capturing

2. Target–drug interactions: first principles and their application to drug discovery

3. High-throughput screening of protein binding by equilibrium dialysis combined with liquid chromatography and mass spectrometry

4. Drug-protein binding mechanism of juglone for early pharmacokinetic profiling: Insights from ultrafiltration, multi-spectroscopic and molecular docking methods

5. Endotoxin Removal from a Small-Molecule Aqueous Drug Substance Using Ultrafiltration: A Case Study

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