2022
DOI: 10.1016/j.ijbiomac.2022.03.113
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An overview on display systems (phage, bacterial, and yeast display) for production of anticancer antibodies; advantages and disadvantages

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Cited by 59 publications
(33 citation statements)
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“…Although antibodies have been widely used as targeting probes, they have several limitations for in vivo imaging, including difficult modification, low binding efficiency, and slow metabolism. 14,15 In contrast, antibody mimetic peptides have gained increasing attention in MR-based molecular imaging due to their fabulous features including easy synthesis, convenient modification and fast binding. 16 We herein report the construction of a collagen-targeting MRI peptide contrast agent for in vivo imaging of hepatic fibrosis (Fig.…”
mentioning
confidence: 99%
“…Although antibodies have been widely used as targeting probes, they have several limitations for in vivo imaging, including difficult modification, low binding efficiency, and slow metabolism. 14,15 In contrast, antibody mimetic peptides have gained increasing attention in MR-based molecular imaging due to their fabulous features including easy synthesis, convenient modification and fast binding. 16 We herein report the construction of a collagen-targeting MRI peptide contrast agent for in vivo imaging of hepatic fibrosis (Fig.…”
mentioning
confidence: 99%
“…In addition, fusion and incorporation of the phage coat protein with its fusion partner occur in the periplasm. This feature is an advantage for several proteins, including secreted heterologous proteins but a disadvantage for cytoplasmic proteins or molecules that have an inhibitory effect on the secretion process, which cannot pass through the inner membrane and cannot be transported to the periplasm to complete the folding and be finally displayed correctly on the phage surface [ 81 ]. To overcome the deficiency of M13, scientists have focused on virulent phage T7 in the field of pathogenic microorganisms.…”
Section: Conclusion and Future Perspectivementioning
confidence: 99%
“…Additionally, biological display systems ensure strict expression regulation and easy library amplification at low cost as well as rapid information decoding of candidates via polymerase chain reaction (PCR) and sequencing. Currently, representative display platforms are phage, bacteria, yeast, ribosome, mRNA, and mammalian cell display systems [17,18]. More importantly, the microplates and microarray chips of libraries or target molecules can be integrated with the above physical detection instruments to establish a high-throughput screening platform, which enables rapid and automatic screening of thousands of samples for affinity toward one or more molecules in parallel [19].…”
Section: High-throughput Screening Using Biological Display Systemsmentioning
confidence: 99%