Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Todd L. Mollan"'
Autor:
John S. Olson, Abdu I. Alayash, Wayne Hicks, Tigist Kassa, Michael Brad Strader, Eileen W. Singleton, Michael T. Wilson, Todd L. Mollan, Mitchell J. Weiss, Jayashree Soman
Publikováno v:
Journal of Biological Chemistry. 289:22342-22357
A pathogenic V67M mutation occurs at the E11 helical position within the heme pockets of variant human fetal and adult hemoglobins (Hb). Subsequent post-translational modification of Met to Asp was reported in γ subunits of human fetal Hb Toms River
Autor:
Yiping Jia, Sambuddha Banerjee, Gang Wu, R. Timothy Kreulen, John S. Olson, Ah-Lim Tsai, Alvin L. Crumbliss, Todd L. Mollan, Abdu I. Alayash
Publikováno v:
Free Radical Biology and Medicine. 69:265-277
Haptoglobin (Hp) is an abundant and conserved plasma glycoprotein, which binds acellular adult hemoglobin (Hb) dimers with high affinity and facilitates their rapid clearance from circulation after hemolysis. Humans possess three main phenotypes of H
Autor:
Eugene Khandros, Joel P. Mackay, Claire F. Dickson, Todd L. Mollan, John S. Olson, Peter A. Lay, Anne M. Rich, Jason A. Lowry, W. d’Avigdor, Daniel A. T. Collins, Mitchell J. Weiss, David A. Gell
Publikováno v:
Journal of Biological Chemistry. 288:19986-20001
α-Hemoglobin (αHb)-stabilizing protein (AHSP) is a molecular chaperone that assists hemoglobin assembly. AHSP induces changes in αHb heme coordination, but how these changes are facilitated by interactions at the αHb·AHSP interface is not well u
Autor:
Ivan Birukou, Todd L. Mollan, Bryan J.Z. Smith, Cornelius L. Varnado, Douglas P. Henderson, John S. Olson
Publikováno v:
Antioxidants & Redox Signaling. 18:2314-2328
Significance: The worldwide blood shortage has generated a significant demand for alternatives to whole blood and packed red blood cells for use in transfusion therapy. One such alternative involves the use of acellular recombinant hemoglobin (Hb) as
Autor:
John S. Olson, Jay N. Lozier, Michael Brad Strader, Abdu I. Alayash, Yiping Jia, Todd L. Mollan, Bindu Abraham
Publikováno v:
Protein Science. 21:1444-1455
Hemoglobin Brigham (β Pro100 to Leu) was first reported in a patient with familial erythrocytosis. Erythrocytes of an affected individual from the same family contain both HbA and Hb Brigham and exhibit elevated O2 affinity compared with normal cell
Publikováno v:
Blood. 113:5961-5969
Alpha hemoglobin stabilizing protein (AHSP) reversibly binds nascent α globin to maintain its native structure and facilitate its incorporation into hemoglobin A. Previous studies indicate that some naturally occurring human α globin mutations may
Autor:
Michael Brad, Strader, Wayne A, Hicks, Tigist, Kassa, Eileen, Singleton, Jayashree, Soman, John S, Olson, Mitchell J, Weiss, Todd L, Mollan, Michael T, Wilson, Abdu I, Alayash
Publikováno v:
The Journal of biological chemistry. 289(32)
A pathogenic V67M mutation occurs at the E11 helical position within the heme pockets of variant human fetal and adult hemoglobins (Hb). Subsequent post-translational modification of Met to Asp was reported in γ subunits of human fetal Hb Toms River
Autor:
Mitchell J. Weiss, Todd L. Mollan, Abdu I. Alayash, Claire J. Parker Siburt, Sambuddha Banerjee, Gang Wu, John S. Olson, Ah-Lim Tsai, Alvin L. Crumbliss
Publikováno v:
The Journal of biological chemistry. 288(6)
α-Hemoglobin stabilizing protein (AHSP) is a molecular chaperone that binds monomeric α-subunits of human hemoglobin A (HbA) and modulates heme iron oxidation and subunit folding states. Although AHSP·αHb complexes autoxidize more rapidly than Hb
Autor:
Todd L, Mollan, Bindu, Abraham, Michael Brad, Strader, Yiping, Jia, Jay N, Lozier, John S, Olson, Abdu I, Alayash
Publikováno v:
Protein science : a publication of the Protein Society. 21(10)
Hemoglobin Brigham (β Pro100 to Leu) was first reported in a patient with familial erythrocytosis. Erythrocytes of an affected individual from the same family contain both HbA and Hb Brigham and exhibit elevated O2 affinity compared with normal cell
Human α-hemoglobin stabilizing protein (AHSP) is a conserved mammalian erythroid protein that facilitates the production of Hemoglobin A by stabilizing free α-globin. AHSP rapidly binds to ferrous α with association (k'(AHSP)) and dissociation (k(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05af8742ca6e84efa0b8310bbf0572c4
https://europepmc.org/articles/PMC3322864/
https://europepmc.org/articles/PMC3322864/