Literature DB >> 26440360

Stable Self-Assembly of Bovine α-Lactalbumin Exhibits Target-Specific Antiproliferative Activity in Multiple Cancer Cells.

Sailendra Mahanta1, Subhankar Paul1.   

Abstract

Self-assembly of a protein is a natural phenomenon; however, the process can be performed under a suitable condition in vitro. Since proteins are nontoxic, biodegradable, and biocompatible in nature, they are used in various industrial applications such as biocatalyst, therapeutic agent, and drug carriers. Moreover, their flexible structural state and specific activity are being used as sensors and immensely attract many new applications. However, the inherent potential of protein self-assembly for various applications is yet to be explored in detail. In this study, spherical self-assembly of bovine α-lactalbumin (nsBLA) was synthesized using an optimized ethanol-mediated desolvation process with an average diameter of approximately 300 nm. The self-assembly was found to be highly stable against thermal, pH, and proteases stress. When nsBLA was administered in various cancer cells, it demonstrated high cytotoxicity in three different cancer cells via reactive oxygen species (ROS) generation, whereas it exhibited negligible toxicity in normal human and murine cells. When nsBLA was conjugated with folic acid, it improved the cytotoxicity and perhaps mediated through enhanced cellular uptake in cancer cells through binding with folate receptors. Further, experimental results confirmed that the cancer cell death induced by nsBLA was not caused by apoptosis but a necrotic-like death mechanism. When compared with a well-known protein-based anticancer agent BAMLET (bovine α-lactalbumin made lethal against tumor cell), the self-assembled BLA clearly exhibited higher cytotoxicity to cancer cells than BAMLET. While BAMLET exhibits poor biocompatibility, our nsBLA demonstrated excellent biocompatibility to normal cells. Therefore, in this study, we prepared self-assembled α-lactalbumin that exhibits strong inherent antiproliferative potential in multiple cancer cells which can be used for efficient therapeutic approach in cancer.

Entities:  

Keywords:  BAMLET; biocompatibility; cellular uptake; self-assembled nanostructured bovine α-lactalbumin; self-assembly

Mesh:

Substances:

Year:  2015        PMID: 26440360     DOI: 10.1021/acsami.5b06076

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  4 in total

Review 1.  α-Lactalbumin, Amazing Calcium-Binding Protein.

Authors:  Eugene A Permyakov
Journal:  Biomolecules       Date:  2020-08-20

2.  Drug-loaded oleic-acid grafted mesoporous silica nanoparticles conjugated with α-lactalbumin resembling BAMLET-like anticancer agent with improved biocompatibility and therapeutic efficacy.

Authors:  Wei Pei; Ling Cai; Xing Gong; Li Zhang; Jiarong Zhang; Ping Zhu; Huijun Jiang; Chao Wang; Shoulin Wang; Jin Chen
Journal:  Mater Today Bio       Date:  2022-05-04

3.  The effect of the type of dietary protein on the development of ovarian cancer.

Authors:  Ahmed A A Taha; Masafumi Koshiyama; Noriomi Matsumura; Kaoru Abiko; Ken Yamaguchi; Jyunzo Hamanishi; Tsukasa Baba; Budiman Kharma; Ibrahim Hassanin Mohamed; Magdy Mohamed Ameen; Salah Ali Ismail; Ikuo Konishi; Masaki Mandai
Journal:  Oncotarget       Date:  2018-05-08

4.  Cytotoxicity of apo bovine α-lactalbumin complexed with La3+ on cancer cells supported by its high resolution crystal structure.

Authors:  Deepthi S Yarramala; Prem Prakash; Dnyanesh S Ranade; Sejal Doshi; Prasad P Kulkarni; Prasenjit Bhaumik; Chebrolu Pulla Rao
Journal:  Sci Rep       Date:  2019-02-11       Impact factor: 4.379

  4 in total

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