A comparative spectroscopic and calorimetric investigation of the interaction of amsacrine with heme proteins, hemoglobin and myoglobin
IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata
View Archive Info| Field | Value | |
| Title |
A comparative spectroscopic and calorimetric investigation of the interaction of amsacrine with heme proteins, hemoglobin and myoglobin
|
|
| Creator |
Bhowmik, Debipreeta
Kumar, Gopinatha Suresh |
|
| Subject |
Chemistry
|
|
| Description |
The binding of the anilido aminoacridine derivative amsacrine with the heme proteins, hemoglobin, and myoglobin, was characterized by various spectroscopic and calorimetric methods. The binding affinity to hemoglobin was (1.21 ± .05) × 105 M−1, while that to myoglobin was three times higher (3.59 ± .15) × 105 M−1. The temperature-dependent fluorescence study confirmed the formation of ground-state complexes with both the proteins. The stronger binding to myoglobin was confirmed from both spectroscopic and calorimetric studies. The binding was exothermic in both cases at the three temperatures studied, and was favored by both enthalpy and entropy changes. Circular dichroism results, three-dimensional (3D) and synchronous fluorescence studies confirmed that the binding of amsacrine significantly changed the secondary structure of hemoglobin, while the change in the secondary structure of myoglobin was much less. New insights, in terms
of structural and energetic aspects of the interaction of amsacrine with the heme proteins, presented here may help in
understanding the structure-activity relationship, therapeutic efficacy, and drug design aspects of acridine
|
|
| Date |
2017
|
|
| Type |
Article
PeerReviewed |
|
| Format |
application/pdf
|
|
| Identifier |
http://www.eprints.iicb.res.in/2668/1/Journal_of_Biomolecular_Structure_and_Dynamics%2C_2017.pdf
Bhowmik, Debipreeta and Kumar, Gopinatha Suresh (2017) A comparative spectroscopic and calorimetric investigation of the interaction of amsacrine with heme proteins, hemoglobin and myoglobin. Journal of Biomolecular Structure and Dynamics, 35 (6). pp. 1260-1271. |
|
| Relation |
http://dx.doi.org/10.1080/07391102.2016.1176958
http://www.eprints.iicb.res.in/2668/ |
|