An in silico analysis on the photoproteins Mnemiopsin 1 and Mnemiopsin 2 to explain the experimental results

Author:

Asadi Sofilar Ashraf1,Shirdel Akram1ORCID,Jafarian Vahab2ORCID,Khalifeh Khosrow13ORCID

Affiliation:

1. Department of Biology, Faculty of Sciences University of Zanjan Zanjan Iran

2. Department of Biology, Faculty of Science University of Guilan Rasht Iran

3. Department of Biotechnology, Research Institute of Modern Biological Techniques University of Zanjan Zanjan Iran

Abstract

AbstractMnemiopsin 1 (Mn1) and Mnemiopsin 2 (Mn2) are photoproteins found in Mnemiopsis leidyi. We have tried to answer the question of whether the structural features of photoproteins can explain the observed activity data. According to the activity measurements data, they have the same characteristic wavelength. However, the initial intensity of Mn2 is significantly higher than that of Mn1, and decay time of Mn1 (0.92 s−1) is lower than that of Mn2 (1.46 s−1). The phylogenetic analysis demonstrates that, compared with Obelin and Aequorin from Obelia longissima and Aequorea victoria, respectively, a gene modification event may have caused the expansion of the N‐terminal side of all photoproteins from M. leidyi. An in silico study has shown that the stability of the photoprotein–substrate complex of Mn2 is higher than that of Mn1, indicating a higher affinity of the substrate for Mn2 compared with Mn1. It was revealed that the active EF‐hand loops 1 and III in Mn2 is locally more rigid compared with those in Mn1. We concluded that different stability of the photoprotein complexes leads to different initial intensity. While different patterns of the local dynamics of loops I and III may influence the decay rate.

Funder

University of Zanjan

Publisher

Wiley

Subject

Chemistry (miscellaneous),Biophysics

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