A comparison of two different analytical workflows to determine the venom proteome composition of Naja kaouthia from North-East India and immunological profiling of venom against commercial antivenoms

被引:13
|
作者
Kakati, Hirakjyoti [1 ]
Patra, Aparup [1 ,2 ]
Kalita, Bhargab [3 ,4 ]
Chanda, Abhishek [1 ]
Rapole, Srikanth [4 ]
Mukherjee, Ashis K. [1 ,2 ]
机构
[1] Tezpur Univ, Dept Mol Biol & Biotechnol, Tezpur 784028, Assam, India
[2] Inst Adv Study Sci & Technol, Div Life Sci, Gauhati 781035, Assam, India
[3] Amrita Vishwa Vidyapeetham, Amrita Inst Med Sci & Res Ctr, Ctr Nanosci & Mol Med, Kochi 682041, Kerala, India
[4] Savitribai Phule Pune Univ Campus, Prote Lab, Natl Ctr Cell Sci, NCCS Complex,Ganeshkhind Rd, Pune 411007, Maharashtra, India
关键词
Indian monocled cobra; LC-MS/MS analysis; Venom proteomics; Venom-antivenom interaction; DABOIA-RUSSELII-RUSSELII; KRAIT BUNGARUS-CAERULEUS; MALAYAN PIT VIPER; PHARMACOLOGICAL-PROPERTIES; MONOCLED COBRA; PATHOPHYSIOLOGICAL SIGNIFICANCE; CLINICAL-MANIFESTATIONS; PHOSPHOLIPASES A(2); SPECTACLED COBRA; NEUTRALIZATION;
D O I
10.1016/j.ijbiomac.2022.03.095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Indian monocled cobra (Naja kaouthia) is one of the most prevalent venomous snakes in northeast India (NEI) and is the cause of many fatalities. The composition of NEI N. kaouthia venom (NkV) was deciphered using two different proteomic approaches: (i) 1D SDS-PAGE coupled to label-free quantification of protein bands using stringent identification criteria and (ii) reversed-phase high-performance liquid chromatography (RP-HPLC) followed by quantification based on area under the RP-HPLC peaks. The proteomic data from both strategies were compared. Proteomic analyses from both workflows identified 32 proteins (toxins) distributed over 10-14 snake venom protein families in NEI NkV. The relative abundances of the venom proteins determined from the analytical workflows coincided with the densitometry band intensities of the NEI NkV. Phospholipase A2 (13.1-16.0%) and three-finger toxins (58.5-64.2%) represented the most abundant enzymatic and non enzymatic proteins in NEI NkV, respectively. Immuno-cross-reactivity studies by enzyme-linked immunoassay and immunoblot analyses pointed to the poor efficacy of commercial PAVs in recognizing the low molecular mass (< 15 kDa) toxins of NEI NkV. Spectrofluorometric titration determined the presence of NEI NkV-specific antibodies in commercial PAV, at a level that was higher than that previously reported for eastern India NkV-specific antibodies in commercial antivenom.
引用
收藏
页码:275 / 287
页数:13
相关论文
共 4 条
  • [1] Comparative analysis of Naja kaouthia venom from North-East India and Bangladesh and its cross reactivity with Indian polyvalent antivenoms
    Deka, Archana
    Abu Reza, Md
    Hoque, Kazi Md Faisal
    Deka, Kamalakshi
    Saha, Sougata
    Doley, Robin
    TOXICON, 2019, 164 : 31 - 43
  • [2] Proteomics of Naja kaouthia venom from North East India and assessment of Indian polyvalent antivenom by third generation antivenomics
    Deka, Archana
    Gogoi, Aditi
    Das, Diganta
    Purkayastha, Jayaditya
    Doley, Robin
    JOURNAL OF PROTEOMICS, 2019, 207
  • [3] Bungarus fasciatus venom from eastern and north-east India: venom variation and immune cross-reactivity with Indian polyvalent antivenoms
    Amit Talukdar
    Anita Malhotra
    H. T. Lalremsanga
    Vishal Santra
    Robin Doley
    Journal of Proteins and Proteomics, 2023, 14 (1) : 61 - 76
  • [4] Proteomics analysis to compare the venom composition between Naja naja and Naja kaouthia from the same geographical location of eastern India: Correlation with pathophysiology of envenomation and immunological cross-reactivity towards commercial polyantivenom
    Chanda, Abhishek
    Patra, Aparup
    Kalita, Bhargab
    Mukherjee, Ashis K.
    EXPERT REVIEW OF PROTEOMICS, 2018, 15 (11) : 949 - 961