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Peptide Library

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A novel nanobody and mimotope based immunoassay for rapid analysis of aflatoxin B1.

Talanta
Mimotopes could replace mycotoxins and their conjugates to develop immunoassay methods. The mimotopes obtained by phage display technology were mainly using monoclonal antibodies or polyclonal antibodies as targets. However, the mimotope of recombina...

[Construction and identification of nanobody phage display library targeting Middle East respiratory syndrome coronavirus].

Xi bao yu fen zi mian yi xue za zhi = Chinese journal of cellular and molecular immunology
Objective To construct a phage display library of specific nano-antibodies against the Middle East respiratory syndrome coronavirus (MERS-CoV) and apply it to the screening of neutralizing nano-antibodies. Methods MERS-CoV receptor-binding domain (RB...

Effective binding to protein antigens by antibodies from antibody libraries designed with enhanced protein recognition propensities.

mAbs
Antibodies provide immune protection by recognizing antigens of diverse chemical properties, but elucidating the amino acid sequence-function relationships underlying the specificity and affinity of antibody-antigen interactions remains challenging. ...

Large-scale network analysis reveals the sequence space architecture of antibody repertoires.

Nature communications
The architecture of mouse and human antibody repertoires is defined by the sequence similarity networks of the clones that compose them. The major principles that define the architecture of antibody repertoires have remained largely unknown. Here, we...

Prosit: proteome-wide prediction of peptide tandem mass spectra by deep learning.

Nature methods
In mass-spectrometry-based proteomics, the identification and quantification of peptides and proteins heavily rely on sequence database searching or spectral library matching. The lack of accurate predictive models for fragment ion intensities impair...

Supervised Learning and Mass Spectrometry Predicts the Fate of Nanomaterials.

ACS nano
The surface of nanoparticles changes immediately after intravenous injection because blood proteins adsorb on the surface. How this interface changes during circulation and its impact on nanoparticle distribution within the body is not understood. He...