4.7 Article

Identification and location of sericin in silkworm with anti-sericin antibodies

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ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.06.044

关键词

Sericin; Antibody; Silk gland; Silkworm

资金

  1. National Natural Science Foundation of China [31972618]
  2. Chongqing Research Program of Basic Research and Frontier Technology [CSTC2018JCYJAX0396]
  3. Project of Innovative Talents Training of Chongqing [CY200239]

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This study for the first time successfully prepared polyclonal antibodies against sericin, confirmed their specificity through dot blot, immunoblotting, and mass spectrometry, and revealed the molecular differences of sericin in different regions and strains of silkworms. Immunohistochemistry showed the different distribution of sericin in the middle silk gland, providing a possible molecular detection method for biological products containing silkworm sericin.
Sericin, as the main component of silkworm cocoon silk, surrounds and protects the silk fibroin. Sericin is a natural macromolecular protein complex encoded by the genes Ser1, Ser2, and Ser3. At present, there are no available antibodies against sericin that may be used to identify and locate it at the protein level, hindering the study of its secretion mechanism and materials application. Therefore, the development of effective antibodies against sericin is an urgent necessity. To address this problem, we prepared polyclonal antibodies against the Ser1, Ser2 and Ser3 proteins using synthesized peptides for the first time. The specificity of the antibodies was confirmed using dot blot, immunoblotting and mass spectrometry on the hybrid bands of the middle silk gland. The immunoblotting results of anti-sericin antibodies showed that sericin has different molecular weights in different regions of the middle silk gland and strains in the 5th instar. Through immunohistochemistry, anti-sericin antibodies revealed that sericin presented different distributions in the anterior part of the middle silk gland of 872 strain at the 7th day of 5th instar. In addition, the prepared antibodies not only detected intact sericin molecules, but also detected degraded sericin that was dissolved in five different solvents. In summary, this work prepared effective sericin antibodies for silk protein synthesis and secretion research and provides a possible molecular detection method for biological products containing silkworm sericin.

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